Human Biology 1995: Vol 67 Index

13 Pages·1995·2.5 MB·English

Index to Volume 67
ABO biood group, 547-559, 595-612, aging effects, 387-406
629-640 agriculture distances, 577-594
aborigines, 37-57 agriculturists, 827-842
abortion ahaptoglobinemia, 37-57
spontaneous, 283-290, 657-672, AK (adenylate kinase), 547-559, 769-778
779-787 Alaskan populations, 407-426
therapeutic, 657-672 Alcantara, V.M., 717-726
a-b ridge count, 121-133 aldosterone, 769-778
‘‘a-b Ridge Count in a Basque Population: Aleuts, 427-458, 459-479
Fluctuating Asymmetry and Algonquian Indians, 355-374, 375-386
Comparison with Other Populations,”’ ‘*Allele and Haplotype Frequency
121-133 Distribution of EcoRI, Rsal, and Msp!
acceleration, 755-767 COL1A2 RFLPs among Various
acid phosphatase (ACP), 37-57, 547-559 Human Populations,’’ 905-920
acid phosphatase 1 (ACP1), 769-778 alleles, 195-215. See also specific alleles
ACP (acid phosphatase), 37-57, 547-559, APOE, 195-215
769-778 apolipoprotein C-H deficiency, 1-36
acrophase, 769-778 associations, 195-215
ADA (adenosine deaminase), 769-778 distribution, 217-229
adenosine deaminase (ADA), 769-778 frequency, 195-215, 311-319, 547-559,
adenylate kinase (AK), 547-559 689-701, 739-753, 789-795, 905-920
adenylate kinase 1 (AK1), 769-778 5’ HVR, 535-546
admixture analysis, 547-559, 717-726, IZHVR, 535-546
843-866 polymorphic, 703-715
adolescents, 739-753 SSTR, 703-715
AFLPs (amplified fragment length Allen, Gordon, 251-263
polymorphisms), 689-701 allotypes, 231-249
Africans, 291-309, 547-559, 905-920. a-globin, 535-546
See also West Africa “*a-Globin Gene Haplotypes in South
ancestry, 311-319 American Indians,’’ 535-546
mitochondrial diversity, 1-36 Alzheimer’s disease, 195-215
age, 111-120, 407-426, 727-738, Amazon, 535-546
827-842 amenorrhea, postpartum, 867-886
biological, 87-109 American ethnic groups, 217-229
distributions, 499-516, 657-672 Amerindians, 231-249, 427-458,
at first pregnancy, 779-787 499-516, 547-559. See also specific
marital, 867-886 Amerindian tribes and Native
maternal, 59-67, 921-931 Americans
at menarche, 739-753, 755-767, amplified fragment length polymorphisms
779-787 (AFLPs), 689-701
of return marriage, 867-886 amyloid plaques, 195-215
964 / Index
ancestral populations, 1-36, 311-319, BCHE locus, 717-726
407-426, 843-866 Bengalis, 843-866
anthropology, 355-374, 819-825 Berba population, 905-920
anthropometry Bhattacharya, Bishwanath, 867-886
analysis, 407-426, 459-479 Bhattacharya, S.K., 827-842
characters, 291-309 biacromial breadth, 459-479
data, 355-374, 387-406, 427-458 biological age, 87-109
distances, 375-386 biological distance, 355-374, 481-498
features, 291-309 biological relationships, 355-374
measurements, 337-344, 727-738, ‘‘Biological Relationships among the
827-842 Iroquois,’’ 355-374
phenotypes, 337-344 biological rhythms, 769-778
traits, 755-767 birth certificates, 755-767
variables, 291-309 birth-cohort analysis, 739-753
antigenic determinants, 231-249 birth order, 59-67, 251-263, 921-931
APOE (apolipoprotein E) gene, 195-215 birth region, 629-640
apolipoprotein C-H deficiency allele, birth registers, 111-120
1-36 birth weight, 135-150, 387-406, 641-656,
apolipoprotein E (APOE), 195-215 755-767
‘*Apolipoprotein E Polymorphism and bivariate analysis, 151-170
Susceptibility to Alzheimer’s Disease,”’ bizygomatic breadth, 459-479
195-215 blacks, 921-931
‘*Application of Two STRs (VWA and Blagitko, N., 217-229
TPO) to Human Population Profiling: blood groups, 769-778
Survey in Galicia,’’ 789-796 ABO, 547-559, 595-612, 629-640
archeology, 427-458 Rh, 547-559
‘*Are the SSTR Alleles Stable Enough To blood pressure, 827-842
Be Considered Monophyletic and blood quantum, 499-516
Hence Reliable Anthropogenetic ‘*Blood Quantum and Ethnic
Markers? Linkage Disequilibrium Study Intermarriage in the Boas Data Set,”’
on the (ACT),, COL1A2 SSTR,”’ 499-516
703-715 BMI (body mass index), 739-753
Arrieta, M.I., 121-133 Boas, Franz, 345-353
Ashkenazi, Israel E., 769-778 Boas anthropometric collection, 337-344
Ashkenazic Jews, 561-576 body dimensions, 291-309
Asians, 905-920, 921-931. See also body mass index (BMI), 739-753
Cambodians, Indian populations, body size, neonatal, 755-767
Japanese, Koreans, Malaysia, Sri body weight, 135-150, 283-290,
Lanka, Thai, Vietnamese 629-640, 739-753
assortative mating, 111-120 Bois, Etienne, 231-249
‘*Assortative Mating: Sex Differences in Bonatto, Sandro L., 547-559
Mate Selection for Married and bones, hand, 87-109
Unmarried Couples,”’ 111-120 book reviewers
asymmetry, fluctuating, 121-133 Amos, Christopher, 517-518
Bayne, Kathryn A.L., 185-188
Bariba population, 905-920 Cameron, Noél, 518-522
Bar-On, H., 151-170 Dyke, Bennett, 181-183
Basque population, 121-133 Gibson, Kathleen R., 959-961
Index | 965
Hall, Teri R., 330-332 Lessons and Other Stories (Neel),
Hixson, James E., 323-325 321-323
Jaquish, Cashell E., 328-330 Primate Social Conflict (Mason and
Korey, Kenneth, 805-807 Mendoza), 185-188
Maki, Susan, 526-529 Sex and Gender Hierarchies (Miller),
McGrath, Janet W., 188-190 325-328
Oths, Kathryn S., 808-810 Species, Species Concepts, and Primate
Pauley, John, 526-529 Evolution (Kimbel and Martin),
Pollitzer, William S., 321-323 522-525
Relethford, John H., 673-676 Bortolini, Maria Catira, 547-559
Rogers, Jeffrey, 522-525 bottlenecks, 1-36
Tardif, Suzette D., 325-328 Brancati, C., 689-701
Willey, P., 183-185 Brazilian Indians, 311-319, 535-546,
Williams-Blangero, Sarah, 179-180 717-726
book reviews breast feeding, 867-886
AIDS and Contemporary History brief communications
(Berridge and Strong), 188-190 ‘*Application of Two STRs (VWA and
Anthropometry: The Individual and the TPO) to Human Population Profiling:
Population (Ulijaszek and Mascie- Survey in Galicia,’’ 789-796
Taylor), 518-522 ‘‘Complete Map of Cystic Fibrosis
Basic Human Genetics (Mange and Mutation DF508 Frequencies in
Mange), 179-180 Western Europe and Correlation
Dancing Skeletons: Life and Death in between Mutation Frequencies and
West Africa (Dettwyler), 330-332 Incidence of Disease,’’ 797-803
Disease and Social Diversity: The “*D1S80 Locus Variability in Three
European Impact on the Health of Non- Brazilian Ethnic Groups,”’ 311-319
“‘Haplotypes without Children: PCR
Europeans (Kunitz), 808-810
Applied to Close Loci on Individual
Evolution (Ridley), 805-807
Handbook of Human Genetic Linkage Human Sperm,”’ 171-178
Bué, C., 703-715
(Terwilliger and Ott), 517-518
Hannah’s Heirs: The Quest for the butyrylcholinesterase (BCHE)
Genetic Origins of Alzheimer’s Disease polymorphisms, 717-726
(Pollen), 181-183 “‘Butyrylcholinesterase Polymorphisms
(BCHE and CHE2 Loci) in Brazilian
The History and Geography of Human
Indian and Admixed Populations,”’
Genes (Cavalli-Sforza et al.), 673-677
717-726
Hominid Culture in Primate Perspective
(Quiatt and Itani), 959-961 Buzhievskaya, Tamara I., 657-672
Human Gene Mapping, 1993: A
Compendium (Cuticchia and Pearson), Caeiro, B., 789-795
323-325 California, 921-931
In the Wake of Contact: Biological Callegari-Jacques, Sidia Maria, 547-559
Responses to Conquest (Larsen and Cambodians, 921-931
Milner), 183-185 Campbell, Janis E., 499-516
Life History Invariants (Charnov), canonical variate analysis, 355-374,
328-330 459-479
The Lopsided Ape (Corballis), 526-529 caste system, 867-886
Physician to the Gene Pool: Genetic Cayuga Indians, 355-374
966 / Index
CFTR (cystic fibrosis transmembrane crown-to-heel length, 135-150
conductance regulator), 561-576, cystic fibrosis, 561-576, 797-813
797-813 cystic fibrosis transmembrane conductance
Chacon-Puignau, Grace, 111-120 regulator (CFTR), 561-576, 797-813
Chautard-Freire-Maia, E.A., 717-726
CHE2 locus, 717-726 **D1S80 Locus Variability in Three
Chen, Jiangtian, 595-612 Brazilian Ethic Groups,’’ 311-319
Chernoby] effect, 657-672 D1S80 polymorphism, 311-319, 689-701
Cherokee Indians, 355-374, 499-516 D12S67 polymorphism, 689-701
child development, 739-753 Das, Ketaki, 933-942
chi-square analysis, 641-656, 843-866 Das, M.K., 933-942
cholesterol, 195-215 Das, Rabindra N., 827-842
chromosomes, 171-178, 195-215, De Benedictis, G., 689-701
535-546, 797-813 De Braekeleer, Marc, 797-803
chronobiology, 769-778 dehydroepiandrosterone sulfate (DHEA-
circadian rhythm, 769-778 S), 769-778
CIS (former Soviet Union), 755—767 delivery outcomes, 657-672
Clegg, J.B., 535-546 De Lourengo, M.A.C., 717-726
climate adaptation, 407-426 De Luca, M., 689-701
cluster analysis, 613-628, 769-778 Demidova, Galina G., 657-672
cohorts, 755-767 demographics, 1-36
Coimbra, Carlos E.A., Jr., 311-319, Dendi population, 905-920
717-726 dendritic analysis, 595-612
COLI1A2 gene, 905-919 dendrograms, 231-249, 427-458,
common ancestor, 1-36 595-612, 769-778
‘‘Common Genetic Influences on BMI dermatoglyphic distance matrices,
and Age at Menarche,”’ 739-753 265-282
‘*‘Complete Map of Cystic Fibrosis De Silvestri, A., 613-628
Mutation DF508 Frequencies in developmental defects, 657-672
Western Europe and Correlation DHEA-S (dehydroepiandrosterone
between Mutation Frequencies and sulfate), 769-778
Incidence of Disease,’’ 797-803 diabetes mellitus, 151-170
computer simulation, 251-263 diachronic comparison, 459-479
Comuzzie, Anthony G., 217-229, ‘Differential Fertility of Mothers of
459-479 Twins and Mothers of Singletons:
congenital anomalies, 657-672 Study in Limon, Costa Rica,’’ 779-787
consanguinity, 535-546 ‘‘Differential Reproductive Success and
contraception, 779-787 Body Dimensions in Kavango Males
correlation component analysis, 577-594 from Urban and Rural Areas in
cortisol, 769-778 Northern Namibia,’’ 291-309
Costa Rica, 779-787 disease(s). See also specific diseases
craniometric studies, 427-458 statistics, 387-406
Crawford, Michael H., 217-229, 459-479, status, 827-842
683-687 distance matrices, 577-594
Cree Indians, 375-386 dermatoglyphic, 265-282
Criado, B., 121-133 genetic, 231-249
cross-cultural analysis, 779-787 Gimbutas hypothesis, 577-594
Crouau-Roy, B., 171-178 Mahalanobis, 481-498
Index | 967
dizygotic twins, 251-263, 739-753, evolution, 111-120, 481-498
779-187 ‘*Evolutionary Relationships between
DNA, 427-458, 535-546 Black South American and African
analysis, 217-229, 689-701 Populations,’’ 547-559
genetic markers, 231-249 exercise, 283-290
probe, 311-319
Doi, Toru, 641-656 facial structure, 459-479
Down syndrome, 657-672 ‘‘Factors Affecting the Sex Ratio in
Dravidian population, 933-942 Humans: Multivariate Analysis of the
Italian Population,’’ 59-67
Dubrova, Yuri E., 755-767
Falcone, E., 689-701
Duggirala, R., 459-479
family
Dugoujon, Jean-Michael, 231-249
correlations, 727-738, 739-753
Dutch famine birth cohort study, 135-150
environmental variables, 727-738
“‘DYS19, D12S67, and D1S80
Germanic, 577-594
Polymorphisms in Population Samples
resemblance, 827-842
from Southern Italy and Greece,”’
family planning, natural, 283-290
689-701
famine, 135-150
DYS19 polymorphism, 689-701
‘Famine, Third-Trimester Pregnancy
Weight Gain, and Intrauterine Growth:
economic factors, 867-886
The Dutch Famine Birth Cohort
EcoRI, 905-920
Study,’ 135-150
ectomorphy, 727-738
fecundity, 867-886
educational achievement, 111-120,
females, 283-290, 769-778. See also
629-640, 827-842
mothers
‘Effect of Interregional Migration on
fertility, 283-290, 291-309, 779-787,
Geographic Variability in Biological
867-886
and Social Traits in Great Britain,”’
depression, 69-86
629-640
regulation, 283-290
“*Effect of Occupation on Menstrual
fertilization efficiency, 59-67
Cycle Length: Causal Model,”’
fetal hemoglobin, 535-546
283-290
Figueiredo, Mauro S., 535-546
Ehlers-Danlos syndrome, 905-920
Finnish twin cohort study, 739-753
endomorphy, 727-738
firstborn proportion, 59-67
Eskimos, 231-249, 427-458
Floris, G., 265-282
esterase D (ESD), 37-57, 769-778 Fon population, 905-920
estradiol, 769-778
founder effect, 535-546, 561-576
‘“*Ethnic Comparison of Twinning Rates in
‘*Franz Boas and Native American
California,’ 921-931
Biological Variability,’’ 345-353
ethnic groups, 87-109, 151-170,
Friedlander, Y., 151-170
407-426, 769-778, 843-866, 921-931
Furuta, Mizuho, 641-656
ethnographic data, 427-458
ethnohistorical data, 427-458 G6PD (glucose-6-phosphate
Europeans, 135-150, 407-426, 547-559, dehydrogenase), 37-57, 547-559
561-576. See also Basque population, Galicia, 789-796
Great Britain, Greece, Italy, Prussia, gametic association, 171-178
Romanians, Russia, Sardinia, Siberia, gender differences, 407-426
Spain, Western Europe a-b ridge count, 121-133
Everson, P.M., 69-86 aging, 87-109
968 / Index
gender differences (cont.) Variation of Mean Birth Weight in
blood pressure, 827-842 Japan,’’ 641-656
mate selection, 111-120 geographic distances, 265-282, 375-386,
parental investment, 291-309 577-594, 595-612
somatotype, 727-738 geographic distributions, 231-249,
gene(s), 121-133. See also specific genes 561-576, 629-640, 797-813
diversity, 547-559, 843-866 ‘‘Geographic Variation of Native People
flow, 337-344, 355-374 along the Pacific Coast,’’ 407-426
frequency, 37-57 Germanic countries, 561-576
locus, 843-866 Germanic family, 577-594
rearrangements, 535-546 gestation, 641-656
genealogy, 1-36 Gil, A., 121-133
‘Genetic Affinities of Sri Lankan Gimbutas hypothesis distance matrix,
Populations,’’ 843-866 577-594
‘‘Genetic and Environmental Influences GLO1 (glyoxalase I), 37-57, 769-778
on Somatotype Components: Family glucose, 151-170
Study in a Spanish Population,” glucose-6-phosphate dehydrogenase
727-738 (G6PD), 37-57, 547-559
genetic distance, 37-57, 231-249, glucose tolerance, 151-170
547-559, 595-612, 769-778, 843-866 glutamic pyruvate transaminase (GPT1),
genetic diversity, 1-36, 231-249, 769-778 769-778
genetic drift, 355-374, 535-546 glyoxalase I (GLO1), 37-57, 769-778
“*Genetic Epidemiology of Blood Pressure GM haplotype frequencies, 231-249
in Two Indian Populations: Some GPT (glutamic pyruvate transaminase),
Lessons,’’ 827-842 769-778
‘*Genetic Evidence on Modern Human Great Britain, 629-640
Origins,’’ 1-36 Great Lakes region, 355-374, 375-386
genetic maps, 217-229, 231-249 Greece, 689-701
genetic markers, 37-57, 769-778 Guerreiro, Joao F., 535-546
genetics, 87-109, 577-594 Guglielmino, C.R., 613-628
analyses, 427-458, 595-612, 789-795 Guitard, Evelyne, 231-249
epidemiology, 827-842 Gupta, Ranjan, 819-825
influences, 739-753
investigation, 337-344 habitat, 407-426
kinship, 887-904 Hall, Don Alan, 407-426
predisposition, 87-109 Hall, Roberta L., 407-426
structure, 613-628 hand, 87-109, 121-133
genetic variance-covariance matrix (G), haplotypes, 535-546, 703-715, 905-920
481-498 ‘*Haplotypes without Children: PCR
genotypes, 311-319, 689-701, 789-795 Applied to Close Loci on Individual
‘Geographic and Ethnic Distributions of Human Sperm,”’ 171-178
the More Frequent Cystic Fibrosis haptoglobins, 37-57, 547-559, 769-778
Mutations in Europe Show That a Hardy-Weinberg equilibrium, 37-57,
Founder Effect Is Apparent for Several 311-319, 789-795, 905-920
Mutant Alleles,’’ 561-576 Harpending-Ward model, 355-374
geographic barriers, 613-628 Haus, Erhard, 769-778
geographic differences, 641-656, 769-778 Hazout, Serge, 231-249, 561-576,
‘Geographic Differences in Seasonal 797-803
Index | 969
HDL (high-density lipoprotein), 195-215 interindividual variation, 171-178
health status, 933-942 intermarriage, 407-426, 499-516
Heath-Carter anthropometric method, intermatch distribution, 1-36
727-738 interobserver error, 337-344
Heidrich, Elisa M., 311-319 interpopulational distances, 265-282
height, 283-290, 387-406, 629-640 interpopulational variation, 265-282
hemoglobin, 37-57, 535-546, 547-559, ‘‘Intersection of Economics, History, and
933-942 Human Biology: Secular Trends in
heterogeneity, 789-795 Stature in Nineteenth-Century Sioux
heterozygosity, 37-57, 547-559, 843-866 Indians,’’ 387-406
high-density lipoprotein (HDL), 195-215 intrauterine growth retardation (IUGR),
Hindus, 867-886 135-150
Hiroshige, Yuka, 641-656 Iroquois Indians, 355-374
histograms, 217-229 island model migration, 1-36
historical birth cohort study, 135-150 isonymy, 613-628
HLA system, 1-36, 171-178, 231-249 Israeli studies, 151-170
Hoff, Charles, 943-947 Italy, 59-67, 613-628, 689-701
hormones, plasma, 769-778 IUGR (intrauterine growth retardation),
‘‘Human Genetic Diversity 135-150
(Immunoglobulin GM Allotypes),
Linguistic Data, and Migrations of Jaffe, Klaus, 111-120
Amerindian Tribes,’’ 231-249 Jantz, R.L., 345-353, 375-386
human population history, 1-36 Japan, 641-656
human thyroid peroxidase (TPO), Japanese, 769-778
789-795 Japanese women, 769-778
Hutz, Mara H., 311-319 Jerusalem, 151-170
HVRs (hypervariable regions), 535-546, Jesup North Pacific Expedition (JNPE),
703-715 345-353
Jews, 151-170, 561-576
immigration, 613-628, 843-866 Jeyaseelan, L., 283-290
immunocompetence, 933-942 Jodice, C., 905-920
‘Immunoglobulin Levels in Populations Jorde, Lynn B., 1-36
with Low Hemoglobin Levels: Study of
Five Tribes of Central India,’’ 933-942 Kahyo, Hiroaki, 641-656
immunoglobulins, 231-249, 933-942 Kamboh, M. Ilyas, 195-215
income, 283-290 Kansas, 69-86
India, 867-886, 933-942 Kaprio, Jaakko, 739-753
Indian populations, 535-546, 827-842, Kark, J.D., 151-170
887-904, 921-931. See also Bengalis Kavango population, 291-309
Indo-Aryans, 933-942 Kholod, Olga N., 755-767
Indo-Europeans, 577--594 Kidron, M., 151-170
Indonesians, 905-920 Kiev, 657-672
infant survival, 135-150 Kirchengast, Sylvia, 291-309, 949-957
infertility, 283-290 Koblyanskaya, Galina N., 657-672
“In Memoriam: Elizabeth Smithgall Kobyliansky, E., 87-109
Watts-Parish (1941-1994),”’ 943-947 Kolmogorov-Smirnov test, 217-229
insulin, 769-778 Konigsberg, Lyle W., 481-498
intergroup relationships, 355-374 Koreans, 921-931
970 / Index
Kshatriya, Gautam Kumar, 843-866 mate selection, 111-120, 355-374
Kurbatova, Olga L., 755-767 matrix correlations, 577-594, 595-612
of genetic distances, 595-612
Langdon, Stephen P., 355-374 of linguistic distances, 595-612
language, 311-319, 375-386, 427-458, Matsuda, Shinya, 641-656
459-479, 577-594 maximum-likelihood estimates, 905-920
LAN (lexicostatistical dissimilarities), maximum linkage cluster, 231-249
577-594 McComb, J., 217-229
Lasker, G.W., 629-640 Meadows, Lee, 375-386
latitude, 407-426 Meloni, G.F., 703-715
Layrisse, Zulay, 547-559 menarche, 739-753, 755-767
LDL-receptor related protein, 195-215 Mennonites, 69-86
least-squares reduction, 217-229 menopause, 867-886
Leonard, W.R., 217-229, 459-479 menstrual cycle, 283-290
lexicostatistical dissimilarities (LAN), mesomorphy, 727-738
577-594 messenger RNA (mRNA), 561-576
LH (luteinizing hormone), 769-778 metacarpal cortical thickness, 87-109
life table estimates, 867-886 Mexican Americans, 217-229
linguistic(s), 37-57, 355-374 MHC (major histocompatibility complex),
data, 231-249, 427-458, 595-612 171-178
distances, 375-386, 577-594, 595-612 microsatellite analysis, 703-715
structure, 595-612 migration, 69-86, 231-249, 921-931
lipoprotein metabolism, 195-215 immigration, 613-628, 843-866
Liu, Y., 37-57 interregional, 629-640
Livshits, G., 87-109 island model, 1-36
Lostao, C.M., 121-133 matrix method, 887-904
Low, P.S., 37-57 miscarriages, 283-290, 657-672, 779-787
Lucotte, Gérard, 561-576, 797-803 mitochondrial DNA (mtDNA), 1-36,
Luis, J.R., 789-795 427-458
Lumey, L.H., 135-150 MMPI personality scales, 739-753
luteinizing hormone (LH), 769-778 mobile site method, 231-249
modeling, bone, 87—109
Madrigal, L., 779-787 Modiano, G., 703-715, 905-920
Mahalanobis, Prasanta Chandra, 819-825 Mohawk Indians, 355-374
Mahalanobis distance matrix, 481-498 monomorphic systems, 37-57
major histocompatibility complex (MHC), monozygotic twins, 251-263, 739-753,
171-178 779-187
Majumder, Partha P., 827-842 Monte Carlo computation, 577-594
Mak, J.W., 37-57 Moore, John H., 499-516
Malaysia, 37-57 morphology, 427-458
males, 265-282, 291-309 mortality, 69-86, 657-672, 779-787
Mantel tests, 265-282, 577-594 ‘*Mortality in a Migrating Mennonite
marital exchanges, 887-904 Church Congregation,’’ 69-86
Martinez, B., 121-133 mothers
Martinson, Jeremy J., 535-546 age at menarche, 755-767
Marwari population, 827-842 correlations with daughters, 739-753
Mascie-Taylor, C.G.N., 629-640 of singletons, 779-787
maternal age, 59-67, 921-931 stature at menarche, 755—767
Index / 971
of twins, 779-787 occupational stress, 283-290
weight gain during pregnancy, 135-150 Oceanic populations, 535-546
Mourrieras, Bruno, 231-249 oligonucleotides, 171-178, 689-701
mRNA (messenger RNA), 561--576 Oneida Indians, 355-374
MspI, 903-917 Onondaga Indians, 355-374
mtDNA (mitochondrial DNA), 1-36, ‘‘Origins of Indo-Europeans and the
427-458 Spread of Agriculture in Europe:
Mukherjee, B.N., 827-842 Comparison of Lexicostatistical and
multiple regression analysis, 283-290, Genetic Evidence,’ 577-594
755-767 Orlandi, P., 703-715
multiregional hypothesis, 1-36 osteography, 87-109
multivariate analysis, 59-67, 231-249, osteoporosis, 87—109
613-628 Ousley, Stephen D., 427-458, 481-498
multivariate quantitative genetics, ‘‘Overview of the Boas Anthropometric
481-498 Collection and Its Utility in
‘*Multivariate Quantitative Genetics of Understanding the Biology of Native
Anthropometric Traits from the Boas North Americans,’’ 337-344
Data,’’ 481-498
mutations, 561-576, 703-715, 797-813 Pacific Islanders, 921-931
palmar main line terminations, 265-282
N1303K cystic fibrosis mutation, 561-576 parents, 111-120, 727-738
Na-Dene, 231-249 path analysis, 827-842
Namibia, 291-309 pathogenic association, 195-215
nasal breadth, 459-479 Pattusali population, 887-904
nasal index, 407-426 Pavlovsky, O., 87-109
nationality, 111-120 PCA (principal components analysis),
Native Americans, 217-229, 337-344, 613-628
345-353, 407-426, 921-931. See also **P.C. Mahalanobis Birth Centenary
specific tribes and Amerindians Symposium on Frontiers of
natural selection, 337-344, 779-787 Anthropology,’’ 819-825
Nayak, Sujata, 827-842 PCR (polymerase chain reaction),
Negritos, 37-57 171-178, 535-546, 689-701, 789-795,
neonates, 755-767 905-920
networks, 887-904 Pepe, G., 703-715, 905-920
neural tube defects, 657-672 perinatal mortality, 657-672
neurofibrillary tangles, 195-215 Petzl-Erler, M.L., 717-726
nonstable population theory, 69-86 PGD (phosphogluconate dehydrogenase),
North Americans, 769-778 37-57, 547-559, 769-778
North Pacific populations, 427-458 PGM1 (phosphoglucomutase 1), 37-57,
Norwich, Jemma, 535-546 547-559, 769-778
noses, 407-426 phenotypes, 121-133, 355-374, 481-498,
Nufiez, M., 121-133 717-726, 905-920
nutrition, 387-406, 459-479, 933-942 phosphoglucomutase 1 (PGM1), 37-57,
547-559, 769-778
obesity, 827-842 phosphogluconate dehydrogenase (PGD),
‘Obituary for Eike-Meinrad Winkler 37-57, 547-559, 769-778
(1948-1994),’” 949-957 phylogeny, 547-559
occupational level, 111-120 Pollard, Richard, 921-931
972 / Index
polymerase chain reaction (PCR), Environmental Factors in Human
171-178, 535-546, 689-701, 789-795, Female Temporal Organization:
905-920 Preliminary Analysis,’ 769-778
‘Polymorphism of Palmar Main Line Prince, Joseph M., 387-406
Terminations As an Indicator of principal components analysis (PCA),
Relationships among Sardinian 613-628
Linguistic Groups of Males,’’ 265-282 17-OH-progesterone, 769-778
polymorphisms, 1-36, 195-215, 231-249, Prokhorovskaya, Valentina D., 755-767
265-282, 769-778 prolactin, 769-778
amplified fragment length, 689-701 proportionality, 481-498
butyrylcholinesterase, 717-726 proteins, 37-57, 769-778
D1S80, 311-319, 689-701 Proto-Malay, 37-57
DNA markers, 171-178 proximate determinants, 291-309
DYS19, 689-701 ‘*Proximate Determinants of Fertility in
HLA, 1-36 Eastern Uttar Pradesh,’’ 867-886
restriction fragment length, 535-546, Prussia, 69-86
703-715, 905-920 pulmonary tuberculosis, 387-406
ponderal index, 135-150
population, 195-215, 231-249. See also quadruplets, 251-263
specific population groups “‘Quantitative Variation in Sets of Triplets
divergence, 355-374 and Quadruplets: A Simulation,”’
expansion, 1-36 251-263
genetics, 37-57, 217-229
postexpansion, 1-36 R553X cystic fibrosis mutation, 561-576
size estimates, 355-374 race differences, 1-36
structure, 375-386 radioactive pollution, 657-672
‘*Population Biology of Human Aging: radiograms, 87-109
Methods of Assessment and Sex rainfall, 407-426
Variation,’’ 87-109 Rao, A. Ramachandra, 887-904
‘‘Population Genetic Study among the Rao, P.S.S., 283-290
Orang Asli (Semai Senoi) of Malaysia: Ravelli, Anita C.J., 135-150
Malayan Aborigines,’’ 37-57 reciprocity, 887-904
‘*Population Relationships among ‘‘Reciprocity in Marital and Social
Historical and Modern Indigenous Networks: Illustration with Indian
Siberians Based on Anthropometric Data,’’ 887-904
Characters,’’ 459-479 red cell enzymes, 37-57
**Population Structure of Algonquian Reddy, B. Mohan, 819-825
Speakers,’’ 375-386 ‘‘Relationships between Eskimos,
postcranial characters, 459-479 Amerindians, and Aleuts: Old Data,
postnatal mortality, 779-787 New Perspectives,’’ 427-458
postpartum amenorrhea, 867-886 religion, 843-866, 867-886
precipitation, 641-656 Renfrew distances, 577-594
pregnancy, 135-150, 657-672, 779-787 replacement hypothesis, 1-36
prematurity, 657-672 reproduction
prenatal care, 135-150 characteristics, 779-787
Preston’s two-census method of isolation, 355-374
demographic estimation, 69-86 strategy, 111-120
‘*Prevalence of Genetic versus success, 291-309