Prenatal Diagnosis 1993: Vol 13 Table of Contents

13 Pages·1993·3 MB·English

PRENATAL DIAGNOSIS
(Prenat. diagn.)
CONTENTS
VOLUME 13, ISSUE Nos. 1-12
Issue No. 1, January
Fetal Blood Sampling and Cytogenetic Abnormalities: J.-D. Liou,
C.-P. Chen, W. R. Breg, J. C. Hobbins, M. J. Mahoney and T. L.
Yang-Feng
An Association Berween Fetal Abdominal Wall Defects ond Elevated
Levels of Human Chorionic Gonadotropin in Mid-Trimester: D.
Schmidt, E. Rose and F. Greenberg.
Prenatal Diagnosis of Syndromes Associating Albinism ond immune
Deficiencies (Chediak-Higashi Syndrome and Variant): A. Durandy,
J. Breton-Gorius, D. Guy-Grand, C. Dumez and C. Griscelli
Early Genetic Amniocentesis—4 Years’ Experience: S. Kerber and
K. R. Held
Prospective Maternal Serum Humen Chorionic Genadowepin Scrveen-
ing for the Risk of Fetal Chromosome Anomalies and of Subsequent
Fetal and Neonatal Deaths: F. Muller, P. Aegerter and A. Boue
Detection of Both the Normal and Mutant Alleles in Single Cells of
Individuals Heterozygous for the Sickle Cell Mutation—Prelude
to Preimplantation — M. Monk, M.-R. ee and
S. Mohadjerani
Association of Goneusiined Dystrophic Raidennshale Bulieee with
Positive Acetylcholinesterase and Markedly Elevated Maternal
Serum and Amniotic Fluid Alpha- aman H. N. Bass, C.
Miranda, R. Oei and B.F. Crandall .
Umbilical Cord Haemangioma Associated with an Eestive Cosmnesue
Haemangioma in a Female Infant: L. K. Weyerts, M. C. Jones,
M. Grafe and A. L. Scioscia
Prenatal Diagnosis of Congenital Cystic Adenomatoid Lung
Malformation: A Report of Seven Cases: A. aeteenneee P. A.
Stewart, J. W. Wiadimiroff and F.J.Los . :
SHORT COMMUNICATION
Prenatal Sonographic Diagnosis of Metastatic Neuroblastoma:
Report of a Case and Review of the Literature: A. J. Jaffa,
A. Many, J. Hartoov, M. J. Kupferminc and M. R. Peyser
Issue No. 2, February
Prenatal Diagnosis of Trisomy 9 Mosaic Presenting as a Case of
Dandy-Walker Malformation: Y.-A. Bureau, W. Fraser and
B. Fouquet ;
Prenatal Diagnosis of Dandy- Walker Malformation ii na Family Dis-
playing X-Linked Inheritance: 7. Cowles, P. Furman and/ . Wilkins .
A Comparison of Amniotic Fluid Alpha-Fetoprotein and Acetyl-
cholinesterase in the Prenatal Diagnosis of Open Neural Tube
Defects and Anterior Abdominal Wall Defects: A. G. A. Loft, E.
Hoagdall, S. O. Larsen and B. Nergaard-Pedersen ; ;
PRENATAL DIAGNOSIS
(Prenat. diagn.)
CONTENTS
VOLUME 13, ISSUE Nos. 1-12
Issue No. 1, January
Fetal Blood Sampling and Cytogenetic Abnormalities: J.-D. Liou,
C.-P. Chen, W. R. Breg, J. C. Hobbins, M. J. Mahoney and T. L.
Yang-Feng
An Association Berween Fetal Abdominal Wall Defects ond Elevated
Levels of Human Chorionic Gonadotropin in Mid-Trimester: D.
Schmidt, E. Rose and F. Greenberg.
Prenatal Diagnosis of Syndromes Associating Albinism ond immune
Deficiencies (Chediak-Higashi Syndrome and Variant): A. Durandy,
J. Breton-Gorius, D. Guy-Grand, C. Dumez and C. Griscelli
Early Genetic Amniocentesis—4 Years’ Experience: S. Kerber and
K. R. Held
Prospective Maternal Serum Humen Chorionic Genadowepin Scrveen-
ing for the Risk of Fetal Chromosome Anomalies and of Subsequent
Fetal and Neonatal Deaths: F. Muller, P. Aegerter and A. Boue
Detection of Both the Normal and Mutant Alleles in Single Cells of
Individuals Heterozygous for the Sickle Cell Mutation—Prelude
to Preimplantation — M. Monk, M.-R. ee and
S. Mohadjerani
Association of Goneusiined Dystrophic Raidennshale Bulieee with
Positive Acetylcholinesterase and Markedly Elevated Maternal
Serum and Amniotic Fluid Alpha- aman H. N. Bass, C.
Miranda, R. Oei and B.F. Crandall .
Umbilical Cord Haemangioma Associated with an Eestive Cosmnesue
Haemangioma in a Female Infant: L. K. Weyerts, M. C. Jones,
M. Grafe and A. L. Scioscia
Prenatal Diagnosis of Congenital Cystic Adenomatoid Lung
Malformation: A Report of Seven Cases: A. aeteenneee P. A.
Stewart, J. W. Wiadimiroff and F.J.Los . :
SHORT COMMUNICATION
Prenatal Sonographic Diagnosis of Metastatic Neuroblastoma:
Report of a Case and Review of the Literature: A. J. Jaffa,
A. Many, J. Hartoov, M. J. Kupferminc and M. R. Peyser
Issue No. 2, February
Prenatal Diagnosis of Trisomy 9 Mosaic Presenting as a Case of
Dandy-Walker Malformation: Y.-A. Bureau, W. Fraser and
B. Fouquet ;
Prenatal Diagnosis of Dandy- Walker Malformation ii na Family Dis-
playing X-Linked Inheritance: 7. Cowles, P. Furman and/ . Wilkins .
A Comparison of Amniotic Fluid Alpha-Fetoprotein and Acetyl-
cholinesterase in the Prenatal Diagnosis of Open Neural Tube
Defects and Anterior Abdominal Wall Defects: A. G. A. Loft, E.
Hoagdall, S. O. Larsen and B. Nergaard-Pedersen ; ;
VOLUME CONTENTS
Prenatal Diagnosis and Management of Anterior Abdominal Wall
Defects in the West of Scotland: A. J. Morrow, M. J. Whittle, M. B.
McNay, P. A. M. Raine, A. A. M. Gibson and J. Crossley.
Low-Dose Sulprostone for Pregnancy Termination in Cases of Fetal
Abnormality: H. H. H. Kanhai and M. J. N. C. Keirse
Adjustment Formulae for Maternal Serum Alpha-Fetoprotein, eenan
Chorionic Gonadotropin, and Unconjugated Oestriol to Maternal
Weight and Smoking: /. Bartels, B. peeseaetiaaiiane B. Bockel,
S. Herold andJ . Caesar
Prenatal Diagnosis of Casnentetne (CMV) indeation: A Prelimi-
nary Report: W. A. Hogge, G. J. Buffone andJ . S. Hogge
SHORT COMMUNICATIONS
Unusual Segregation for 11q;22q Parental Translocation in a Triplet
Pregnancy: Prenatal Diagnosis in Chorionic Villi and Amniotic
Fluid: A. Soler, A. Carrio, M. T. Perez-Vidal, A. Borrell and
A. Fortuny
Prenatal Diagnosis of Hb H Diseases yn to» Conmeund Netwreevee-
sity for South-East Asian Deletion and Hb Constant Spring by
Polymerase Chain Reaction: 7.-M. Ko, L.-H.a sieadsF .-J. Hsieh
and T.-Y. Lee ; : ;
LETTERS TO THE EDITOR
Prenatal Diagnosis for Cystic Fibrosis Using SSCP Analysis:
M. Desgeorges, P. Boulot, P. Kjellberg, G. Lefort, M. Rolland,
J. Demaille and M. Ciaustres
Prenatal Diagnosis of Zellweger Seadene u4 sing ‘DNA poarerm
N. Shimozawa, Y. Suzuki, T. Orii, T. Tsukamoto and Y. Fujiki
Prenatal Detection of Succinic a Dehydrogenase
Deficiency (4-Hydroxybutyric Aciduria): C. Jakobs, H. —
D. Rabier and K. M. Gibson .
Genomic Imprinting, Human Chorionic Genedewegin, ond
Triploidy: D. Haig ;
Prenatal Diagnosis of Tetrasomy 12p (Pallister- Killian Senden:
J. H. Priest
Maternal Serum Sereening Risk for Down Syndrome ii s Considered
Positive if a Triple-marker-derived Risk Exceeds the Age- Specific
Risk: Use of this Definition for Women — 35 and Over:
J. Fitzgerald, K. Streets and J. Priest ;
ANNOUNCEMENT .
Issue No. 3, March
Preterm Delivery Rate and Fetal Outcome in Structurally Affected
Twin Pregnancies: A Retrospective Matched Control Study: A.
Heydanus, J. G. Santema, P. A. Stewart, P. G. H. Mulder and
J. W. Wladimiroff
Prenatal Detection of Monsen 21 Mosaicism: A. Ghidini. S. Fallet,
J. Robinowitz, C. J. Lockwood, R. Dische andJ . Willner
Heteroduplex Formation: A Potential Source of Genotyping Error hom
PCR Products: S. L. S. Hatcher, Q. a Lambert, R. L. a and
J. R. Carlson
vi VOLUME CONTENTS
Mosaicism in Chorionic Villus Sampling: An Analysis of Incidence and
Chromosomes Involved in 2612 Consecutive Cases: 8B. B. 7. Wang,
C. H. Rubin and J. Williams II/
Racial Differences in Maternal Serum omen, Chndesie Guano
tropin and Unconjugated Oestriol Levels: P. Ku/ch, S. Keener,
M. Matsumoto and B. F. Crandall
Risk Evaluation of CVS: A. M. Kuliev, B. Modell, L. Jecheon, J L.
Simpson, B. Brambati, G. Rhoads, U. Froster, Y. Verlinsky, S.
Smidt-Jensen, W. oo N. — P. Ammala and Y.
Dumez ;
SHORT COMMUNICATIONS
Complex Mosaicism Associated with Trisomy 9: /. S. Smo/eniec,
T. Davies, P. Lunt, P. J. Berry andD . James .
First- Trimester Alpha-Fetoprotein Screening for Down Syadbeme:
W. Fuhrmann, K. Altland, V. Jovanovic, W. a P. —
D. Wenger and R. Rauskolb .
LETTERS TO THE EDITOR
Direct Prenatal Diagnosis of Friedreich’s Disease: A. Richter, J.
Poirier, J.M ercier andS . B. Melancon .
Poor Pregnancy Outcome Associated with Elevated Maternal
Serum Alpha-Fetoprotein in Combination with Increased Risk for
Down Syndrome: C. P. Walters
Pregnancy Associated Plasma Protein A as a Marker fer Dew
Syndrome in the Second Trimester of Pregnancy: G. J. Knight,
G. E. Palomaki, J. E. Haddow, W. Miller, N. A. inet and
H. Schneider
Low Maternal Serum Oestriol and Chorionic Genadewesia in the
Prediction of Adverse Pregnancy Outcome: G. Mason, S. Lindow,
C. Ramsden, H. Cuckle andS . Holding
Vaginosonography and Chorionic Villus Sampling (CVS): G.
Ghirardini andL . W. Popp
A Further Case of Prenatally Detected Mosaic eshunnnenenn 204:
C. Cooper, A. Fifer and K. Ocraft . 3
Alpha-Fetoprotein and Acetylicholinesterase are not Predictors ot
Fetal Junctional Epidermolysis Bullosa, Herlitz Variant: L. P.
Shulman, S. Elias, J. L. Simpson, K. A. Holbrook, L. T. Smith and
J.-D. Fine
First Trimester penniacentesia Sevanen the Seventh ond 13th
Weeks: Evaluation of the Earliest Possible Genetic Diagnosis:
N. C. Wathen, D. J. Campbell and T. Chard. ;
Authors’ Reply: /. Kennerknecht, D. Grab and R. ——
ANNOUNCEMENT .
Issue No. 4, April
Rapid Detection of Aneuploidy in Uncultured Chorionic Villus Cells
Using Fluorescence in situ Hybridization: P. N. Rao, R. —-
K. Cox, F. Grass and M. J. Pettenati
‘Late’ Chorionic Villus Sampling: Cregenstic hapeue L Dalpra,
G. Nocera, M. G. Tibiletti, E. Martinoli, A. Oldrini, S. — and
P. G. Crosignani
VOLUME CONTENTS
Evaluation of Amniotic Fluid Cell Filtration: An Experimental Ap-
proach to Early Amniocentesis:/ .K ennerknecht, S. Kramer, D. Grab
and R. Terinde.
A Prospective Cytogenetic Study of Third- Thimenter Plesentes in
Small-for-Date But Otherwise Normal Newborns: /. Kennerknecht,
S. Kramer, D. Grab, R. Terinde and W. Vogel
Second-Trimester Unconjugated Oestriol Levels in Maternal Serum
From Chromosomally Abnormal Pregnancies Using an a
Assay: J. A. Crossley, D. A. Aitken and J.M . Connor
Economic Assessment of Maternal Serum Screening for Down's Syn-
drome Using Human Chorionic Gonadotropin: V. Seror, F. Muller,
J. P. Moatti, C. Le Gales andA . Boue
Erythroid-Specific Antibodies Enhance Detection of Fetal Nucleated
Erythrocytesi n Maternal Blood: D. W. Bianchi, G. K. Zickwolf, M. C.
Yih, A. F. Flint, O. H. Geifman, M. S. Erikson and J. M. Williams
SHORT COMMUNICATION
Evidence of a Second Gamete Fusion After the First Cleavage of the
Zygote in a 47,XX, +18/70,XXX, +18 Mosaic. A Remarkable
Diploid-Triploid Discrepancy After CVS: J. H. A. M. a
A. S. P. M. Breed, R. Vosters and G. J. P. A. Anders
LETTER TO THE EDITOR
Trisomy 15 in Chorionic Villi and Prader-Willi Syndrome at Birth:
N. Morichon-Delvallez, P. Mussat, Y. Dumez and M. Vekemans .
ERRATUM
Issue No. 5, May
Cytogenetic Analysis of Human Oocytes After Subzonal !nsemination:
J. Selva, J. P. Wolf, P. Rince, D. en R. a and P.
Jouannet :
Dystrophin Gene Analysis ond Pronnal Diagnosis of ashes
Muscular Dystrophy in Russia: V. S. Baranov, V. N. Gorbunova,
O. V. Malysheva, O. V. Artemyeva, T. K. Kascheeva, O. V. Evgrafov,
A. V. Polyakov, V. M. Lebedev, T. V. Kuznetzova, S. N. —
A. V. Mikhailov and V. G. Vakharlovsky
Applicability of DNA Isolated from Synertawenhatinn Vestine to
Gene Amplification and Molecular Analysis: G. Co/ucci, E. Pesenti,
E. Molteni, A. Lobbiani, C. De Andreis, S. Pariani, F. Rossella, A. E.
SempriniandG. Simoni .
Grief and Mid-Trimester Fetal Loss: M. Seller, C. Sesaen s. pn T.
Barby and P. Cowmeadow
Rapid Karyotyping in Ectopic Pregnancies: D. Cohen, /. Denes, C.
Berta, M. Fodor, E. Alonso, C. Nasio, L. Kreiman and R. Pineda
Characterization of i(18p) in Prenatal Diagnosis by Fluorescence in
situ Hybridization: L.-C. Yu, J. Williams //1, B. B. T. Wang, M. eee
H.-U. G. Weier, M. Sakamoto and K.-L. Ying .
False-Positive Amniotic Fluid Acetylicholinesterase Anaivele in the
Third Trimester: S. F. Suchy and M. T. Yeager .
First-Trimester Diagnosis of Duodenal Stenosis pasociated with
Oesophageal Atresia: G. L. Tsukerman, G. A. —_— and| . A.
Kirillova , .
Vili VOLUME CONTENTS
A Large Retinoblastoma Detected in a Fetus at 21 Weeks of Gestation:
J. A. Maat-Kievit, D.O epkes, N. G. Hartwig, C. a Keers, /. L.
Van Kamp and J. J. P. Van de Kamp
Molecular Cytogenetic Characterization of on Chee
Found at Prenatal Diagnosis: M. R. Verschraegen- nomN . Van a
A. De Perdigo, A. De Paepe andF .S peleman .
SHORT COMMUNICATIONS
Ultrasonographic Features in a Case of Heterozygous Achondro-
plasia at 25 Weeks’ Gestation: M. Cordone, M. Lituania, G.
Bocchino, U. Passamonti, P. Tomé andG . Camera
Prenatal Diagnosis of Isolated Bilateral Microphthelmia with
Confirmation by Evaluation of Products of Conception Obtained
by Dilation and Evacuation: L. P. Shu/man, P. L. Gordon, D. S.
Emerson, R. S. Wilroy andS . Elias
Early Prenatal Sonographic Diagnosis of enmnniide hatte
gryposis Multiplex Congenita with Osseous Heterotopia: F.
Gullino, M. Abrate, E. Zerbino, G. Bricchi and P. D. Rattazzi
Prenatal Diagnosis of Exencephaly: M. Casel/las, M. Ferrer, M.
Rovira, F. Pla, M. A. Martinez and L. Cabero : ; ;
LETTERS TO THE EDITOR
Elevated Maternal Serum Alpha-fetoprotein, Very Low Unconju-
gated Oestriol, and Very Low Human Chorionic Gonadotropin
Associated with Recent Fetal Death: C. P. Walters and W. C.
McKinnon
Turner Syndrome po with ane w D. N.S aller Sr.
J. V. Dailey, D. L. Doyle, S. R. Carr, J. A. Canick and B. B. Rogers
Issue No. 6, June
B-Glucuronidase Deficiency: Identification of an Affected Fetus with
Simultaneous Sampling of Chorionic Villus and Amniotic Fluid:
A. Chabas and A. Guardiola
Prenatal Exclusion of X-Linked Reteneneien: eek of the
Aqueduct of Syivius Sequence Using Closely Linked DNA Markers:
F. Serville, P. Benit, P. Saugier, M. Vibert, G. — A. Pelet, M.
Chery, A. Munnich and S. Lyonnet.
Prenatal Diagnosis of Ornithine eee a Results
in SPF*S" Mice: K. Monastiri, D. Rabier and P. Kamoun .
Short Femur Length Associated with Severe Intrauterine Growth
Retardation: 8. Bromley, D. L. Brown and B. R. Benacerraf
Evaluation of Prenatal Diagnosis of Congenital Heart Disease: C. Sto//,
Y. Alembik, B. Dott, P. M. Roth and B. De Geeter
Antenatal Thrombocytopenia in Three Patients with TAR _—
cytopenia with Absent Radii) Syndrome: Ph. Labrune, J. C. Pons,
M. Khalil, V. Mirlesse, M. C. Imbert, M. Odievre, F. Daffos, G.
Tchernia and R. Frydman
Maternal Serum Biochemical Markers in —— with ‘Fetal
—™ B19 Infection: D. N. Saller Jr., B. Barton — A.
anick
VOLUME CONTENTS
Quantification of Human Amniotic Fluid Constituents by High Resol-
ution Proton Nuclear Magnetic Resonance (NMR) Spectroscopy:
C. J. Sims, D. T. Fujito, D. R. Burholt, J.D adok, H. R. Giles and D.
Allan Wilkinson
Follow-up of Pane Complicated o Placental on
Diagnosed by Chorionic Villus Sampling: J. S. royeune, M. S.
Dimaio, T. L. Yang-Feng and M. J. Mahoney. :
Disappearing Lung Echogenicity in Fetal Ricteaeenbennes. Mal-
formations: A Reassuring Sign?: S. E. Meagher, N. M. Fisk, J. G.
Harvey, G. F. Watson and A. Boogert , .
Sonographic Diagnosis of Fetal Congenital Cataracts: —. Z. Zimmer,
M. Bronshtein, E. — |. Meizner, R. Auslender, G. Groisman and
H. Meyer.
SHORT COMMUNICATIONS
Ultrasound Screening for Chromosomal Anomalies in the First Tri-
mester of Pregnancy: G. Savo/delli, F. Binkert, J.A chermann and
W. Schmid . ;
Prenatal Transvaginal re of the Seneteante, Seutened
Dysplasia, Cleft Palate mente —— M. Bronshtein and R.
Gershoni-Baruch .
Achondrogenesis Type 2 —_— by emeniieel vo at
12 Weeks’ Gestation: P. W. Soothill, C. Vuthiwong and H. Rees .
First Report of Prenatal Diagnosis of Long-chain 3-Hydroxyacyl-
CoA Dehydrogenase Deficiency in a Pregnancy at Risk: C.
Perez-Cerda, B. Merinero, A. Jimenez, M. J. Garcia, P. Sanz, L.
Iilst, R. J. A.W anders and M. Ugarte
A Comparison of Total and Free 8- HCG Assays in —_— Saban
Screening: S. Stone, R. Henley, T. Reynolds and R. John
Myasthenia Gravis with Polyhydramnios in the Fetus of an Asymp-
tomatic Mother: E. Verspyck, L. Mandelbrot, M.D ommergues, C.
Huon, F. Woimant, C. Baumann and B. Vernet-Der Garabedian .
LETTER TO THE EDITOR
Improvement of rDNA-based PCR Assay to Detect eepemeaten J.
Cazenave, A. Cheyrou andJ . Begueret ‘
ERRATUM
Issue No. 7, July
Fetal Renal Artery Flow Velocity Waveforms in the Presence of Con-
genital Renal Tract Anomalies: J. W. Wladimiroff, R. — P.A.
Stewart, T. E.C ohen-Overbeek and Ch. Brezinka
The Diagnostic Potential of Fetal Renal Biopsy: P. Greco, G. panei
G. Caruso, R. Clemente and L. Selvaggi . ;
First-Trimester Free Beta (hCG) Screening for Down enn J. N.
Macri, K. Spencer, D. Aitken, K. Garver, P. D. Buchanan, F. Muller
andA . Boue
First- Trimester Maternal as Sema Protein 1 (SP1) in
Pregnancies Associated with Chromosomal Anomalies: M. C. M.
Macintosh, 8B. Brambati, T. Chard and J. G. Grudzinskas
x VOLUME CONTENTS
A Rare Inherited Euchromatic Heteromorphism on Chromosome 1: A.
L. Zaslav, D. Blumenthal, J. E. Fox, K. A. Thomson, R. ane and
M. W. Weinstein
Walker-Warburg Syndrome: a uwensund Findings: N. Vohra,
A. Ghidini, M. Alvarez andC . Lockwood .
Prenatal Diagnosis by jn situ Hybridization on Uneutened fuasio
cytes: Reduced Sensitivity and Potential Risk of Misdiagnosis in
Blood-Stained Samples: 8B. Christensen, T. Bryndorf, J. Philip, Y.
Xiang and W. Hansen
First- Trimester Prenatal Diagnosis of Ocnsogonesis ipartacte hee r
by DNA Analysis and Sonography: M. S. Dimaio, R. Barth, K. E.
Koprivnikar, B. L. Sussman, J. A. Copel, M. J. Mahoney, P. H. Byers
and D. H. Cohn
Transvaginal Sonographic Detection ofS keletal Anomalies! in the First
and Early Second Trimesters: M. Bronshtein, D. Keret, M. Deutsch,
A. Liberson and| .B ar Chava
Emotional Reactions in Women in Late rensenee (24 Weeks or
Longer) Following the Ultrasound Diagnosis of a Severe or Lethal
Fetal Malformation: J. A. M. Hunfeld, J. W. Wladimiroff, J.
Passchier, M. U. Venema-Van Uden, P. G. Frets and F. Verhage
Attitudes of Women of Childbearing Age Towards Prenatal Diagnosis
in Southeastern France: C. Julian-Reynier, G. Macquart-Moulin,
J.-P. Moatti, A. Loundou, Y. Aurran, F. ChabalandS.Aymé .
Prenatal Diagnosis of Gastrointestinal Obstruction: A Correlation
Between Prenatal Ultrasonic Findings and Postnatal Operative
Findings: C. A. Del/ —— V. Tomaselli, E. Teruzzi, B. Tadiniand A.
G. Coran .
SHORT COMMUNICATIONS
Serum PAPP-A Levels are Depressed in Women with Fetal Down
Syndromei n Early Pregnancy: F. Muller, H. Cuckle, B. Teisner and
J. G. Grudzinskas
46,XY/47,.XY,+17p+ Mosaiciem i2n Amnlenpes Associated with
Fetal Abnormalities Despite Normal Fetal Blood Karyotype: H. M.
Kingston, U. Nicolini, J.H aslam and T. Andrews .
Prenatal Diagnosis of the Acute Form of Proximal Spinal Museuter
Atrophy: Experience on the Acceptance of Linkage Analyses by
the Families: J.H uschenbett, R. Hanke, L. Pfeifer and A. Speer
Successful DNA-Based Prenatal Exclusion of Juvenile Neuronal
Ceroid Lipofuscinosis: P. Uvebrant, E. Bjorck, N. Conradi, K.-H.
Hokegard, T. Martinsson and J. Wahlstrom.
LETTERS TO THE EDITOR
Bilateral Pleural Effusion at 8-5 Weeks’ Gestation with Down Syn-
drome and Turner Syndrome: A. Cadkin and E. Pergament .
Prenatal Diagnosis of Huntington's disease: D. Wa//erstein
Issue No. 8, August
Fluorescent in situ Hybridization (FISH): A New Application in the
Delineation of True vs Pseudomosaicism in Prenatal Diagnosis:
S. Schwartz and J. Leana-Cox . ‘ : : 7
VOLUME CONTENTS
Molecular Cytogenetic Analysis of Term Placentae Suspected of
Mosaicism Using Fluorescence jin situ Hybridization: G. H.
Schuring-Blom, M. Keijzer, M. E. Jakobs, D. M. van den Brande,
H. M. Visser, J. Wiegant, J. M. N. Hoovers and N. J. Leschot .
First- Trimester Biochemical Screening for Fetal Chromosome Abnor-
malities and Neural Tube Defects: D. A. Aitken, G. McCaw, J. A.
Crossley, E. Berry, J.M . Connor, K. Spencer and J.N. Macri .
is Selective Abortion for a Genetic Disease an Issue for the Medical
Profession? A Comparative Study of Quebec and France: M.
Renaud, L. Bouchard, O. aes L. Dallaire, J. F. Labadie, J. Bisson
and A. Trugeon
Attitudes Toward Abortion ns Fetal paamiate'i n ‘the Seemed vs Third
Trimester: A Survey of Parisian Obstetricians: G. Geller, E. S. Tambor
and E. Papiernik
Cytogenetic Analysis of 2928 cvs Reet and 1075 hannieneenues
From Randomized Studies: S. Smidt-Jensen, A.-M. Lind, M.
Permin, J. M. Zachary, C. Lundsteen and J. Philip.
Women’s Opinions on the Offer and Use of Maternal Serum ——-
ing: E. E. C. Roelofsen, L. |. Kamerbeek, TJ. —— J. R. Beekhuis
and A. Mantingh :
Measurement of the Fetal Mandible—Feasibility _ — aea
Centile Chart: L. S. Chitty, S. Campbell and D. G. Altman
SHORT COMMUNICATIONS
Verification of Carrier Status for Becker Muscular Dystrophy From
Analysis of a — Ovum: S. D. Wilton, J. Goldblatt and
N.G. Laing . ;
On the Parental Origin of the X's in a — Seneneid
49,XXXXX Syndrome: G. Martini, G. Carillo, F. Catizone, A.
Notarangelo, R. Mingarelli and B. Dallapiccola
LETTERS TO THE EDITOR
How Accurate Does Rapid Fetal Karyotyping Need to be? Case
of Unbalanced t(13;18): J. Jackson, L. Robson, S. —
G. Watson and A. Smith
Fetal Karyotype from Cystic Retenn Fluid: Diploid/Tetraploid
Mosaicism: C. Piquet, M. Gamerre, A. a. C. Scheiner and
N. Philip :
First-Trimester Prenatal neuer - Non- Ketotic Hyperglycinae-
mia by a Micro Assay of Glycine a — M. O. Rolland,
G. Mandon and M. Mathieu
Prenatal Diagnosis of Spina Bifida — — First-h ese
Valproate Exposure: S. Guibaud, E. Robert, A. saieaiis Cc.
Boisson, C. Francannet and M.-H. Patouraux
Second-Trimester CA 125 and Down’s Syndrome: K. Sew
Issue No. 9, September
Magnetic Resonance Imaging of the Fetus: A Study of 20 Cases
Performed Without Curarization: M. P. Revel, J. C. Pons, C.
Lelaidier, P. Fournet, M. Vial, D. Musset, M. Labrune and R.
Frydman .
xii VOLUME CONTENTS
Cytogenetic Analysis of 1375 Amniotic Fluid Specimens from Preg-
nancies with Gestational Age Less Than 14 Weeks: D. H. Lockwood
andR.L.Neu .
Prenatal Cystic Fibrosis Carrier Screening: Fectors in a - Woman'ss
Decision to Decline Testing: M. E. Mennie, A. Gilfillan, M. E.
Compton, W. A. Liston and D. J. H. Brock
Rapid Detection of Numerical Aberrations of Cheemenemee 13, 18
and 21 in Chorionic Mesenchymal Cells: 7. — B.
Christensen, Y. Xiang, A-M. Lind and J. Philip :
Application of Fluorescent jn situ Hybridization for ‘de novo’
Anomalies in Prenatal Diagnosis: D. Van Opstal, H. J. Eussen, J. O.
Van Hemel and E. S. Sachs
Fetal Tissue Involvement in the Late Infantile — of a Coroid
Lipofuscinosis: C. W. Chow, J. Borg, V. R. Billson and B. D. Lake .
Expanding Multiple Marker Screening for Down's Syndrome to
Include Edward's Syndrome: G. Barkai, B. Goldman, L. Ries, R.
Chaki, T. Zer and H. Cuckle
Prenatal Diagnosis of Gall Bladder Anomalies ~ - Report of 17 Cases:
M. Bronshtein, Z. Weiner, H. Abramovici, S. Filmar, Y. Erlik and Z.
Blumenfeld A
The Early Diagnosis of Neural Tube Defects: Z. Blumenfeld, E. Siegler
and M. Bronshtein .
Polymerase Chain Reaction peahain of the Cystic Plasesie AF508
Mutation in Human Blastomeres Following Oocyte Injection of a
Single Sperm from a Carrier: J. Liu, W. Lissens, P. eens A. Van
Steirteghem and| . Liebaers
SHORT COMMUNICATION
Prenatal Diagnosis of DHPR Deficiency by Direct Detection of
Mutation: P. M. Smooker, R. G. H. Cotton and A. Lipson
LETTERS TO THE EDITOR
A Triploid Fetus with a Diploid Placenta: Proposal of a Mechanism:
/. Kennerknecht, W. Just and W. Vogel
Calculating Amniotic Fluid Alpha-fetoprotein Median Values in the
First Trimester: G. E. Palomaki, G. J. Knight andJ . E. Haddow
Unusual aie for soa Parental Translocation: J. E.
Allanson
Authors’ Reply: A. Soler, A. Carié, M. T. Pérez- Vidal, A. Senet
and A. Fortuny. :
Issue No. 10, October
Familial Congenital Diaphragmatic Hernia: Prenatal Diagnosis, Man-
agement, and Outcome: H. Narayan, R. de Chazal, M. Barrow,
P. McKeever and E. Neale
Serum PAPP-A Measurements in First- Trleneater Sercening for Down
Syndrome: P. A. Hurley, R. H. T. Ward, B. Teisner, R. K. Iles, M. Lucas
andJ . G. Grudzinskas
Preaxial Ray Reduction Defects as Part of Valproic Acid ~——
fetopathy: AR. Sharony, A. Garber, D. Viskochil, R. Schreck, L. D.
Platt, R. Ward, B. A. Buehler and J.M . Graham, Jr .