Works matching IS 01973851 AND DT 1996 AND VI 16 AND IP 2

Results: 18

PRENATAL DIAGNOSIS OF ROBERTS SYNDROME: TWO NEW CASES.

Published in:

Prenatal Diagnosis, 1996, v. 16, n. 2, p. 125, doi. 10.1002/(SICI)1097-0223(199602)16:2<125::AID-PD822>3.0.CO;2-S

By:

BENZACKEN, B.;
SAVARY, J. B.;
MANOUVRIER, S.;
BUCOURT, M.;
GONZALES, J.

Publication type:

Article

BLOOD CONTAMINATION OF AMNIOTIC FLUID AFTER AMNIOCENTESIS IN RELATION TO PLACENTAL LOCATION.

Published in:

Prenatal Diagnosis, 1996, v. 16, n. 2, p. 180, doi. 10.1002/(SICI)1097-0223(199602)16:2<180::AID-PD833>3.0.CO;2-B

By:

GIORLANDINO, CLAUDIO;
GAMBUZZA, GIOVANNI;
D'ALESSIO, PAOLO;
SANTORO, MARIA LUISA;
GENTILI, PAOLO;
VIZZONE, ANTONIO

Publication type:

Article

MULTIPLE FETAL INTRACARDIAC ECHOGENIC FOCI: NOT ALWAYS A BENIGN SONOGRAPHIC FINDING.

Published in:

Prenatal Diagnosis, 1996, v. 16, n. 2, p. 131, doi. 10.1002/(SICI)1097-0223(199602)16:2<131::AID-PD823>3.0.CO;2-Q

By:

BRONSHTEIN, MOSHE;
JAKOBI, PETER;
OFIR, CHAGIT

Publication type:

Article

Announcement.

Published in:: Prenatal Diagnosis, 1996, v. 16, n. 2, p. I, doi. 10.1002/pd.1970160218
Publication type:: Article

CLINICAL EXPERIENCE WITH PREIMPLANTATION GENETIC DIAGNOSIS OF CYSTIC FIBROSIS (ΔF508).

Published in:

Prenatal Diagnosis, 1996, v. 16, n. 2, p. 137, doi. 10.1002/(SICI)1097-0223(199602)16:2<137::AID-PD824>3.0.CO;2-H

By:

AO, ASANGLA;
RAY, PIERRE;
HARPER, JOYCE;
LESKO, JOHN;
PARASCHOS, THANOS;
ATKINSON, GLENN;
SOUSSIS, IAKOVOS;
TAYLOR, DEBBIE;
HANDYSIDE, ALAN;
HUGHES, MARK;
WINSTON, ROBERT M. L.

Publication type:

Article

FIRST-TRIMESTER PRENATAL DIAGNOSIS OF CROUZON SYNDROME.

Published in:

Prenatal Diagnosis, 1996, v. 16, n. 2, p. 155, doi. 10.1002/(SICI)1097-0223(199602)16:2<155::AID-PD826>3.0.CO;2-7

By:

SCHWARTZ, MARIANNE;
KREIBORG, SVEN;
SKOVBY, FLEMMING

Publication type:

Article

PRENATAL DETECTION OF TWO DIFFERENT MONOSOMIC CELL LINES BY CHORIONIC VILLUS SAMPLING.

Published in:

Prenatal Diagnosis, 1996, v. 16, n. 2, p. 169, doi. 10.1002/(SICI)1097-0223(199602)16:2<169::AID-PD819>3.0.CO;2-T

By:

HSU, TE-YAO;
LIOU, JUI-DER;
COPEL, JOSHUA A.;
MAHONEY, MAURICE J.;
BREG, W. ROY;
YANG-FENG, TERESA L.

Publication type:

Article

LETTER TO THE EDITOR. Multiple-marker Screen Positive Results in Noonan Syndrome.

Published in:

Prenatal Diagnosis, 1996, v. 16, n. 2, p. 183, doi. 10.1002/(SICI)1097-0223(199602)16:2<183::AID-PD850>3.0.CO;2-F

By:

ARANGUREN, GABRIEL;
GARCÍA-MIÑAUR, SIXTO;
LORIDAN, LILIANE;
URIBARREN, ADOLFO;
MARTÍN VARGAS, LUCI;
RODRÍGUEZ-SORIANO, JUAN

Publication type:

Article

PRENATAL ULTRASOUND FINDINGS IN HYDROLETHALUS: CONTINUING DIFFICULTIES IN DIAGNOSIS.

Published in:

Prenatal Diagnosis, 1996, v. 16, n. 2, p. 173, doi. 10.1002/(SICI)1097-0223(199602)16:2<173::AID-PD821>3.0.CO;2-I

By:

NORGARD, MICHAEL;
YANKOWITZ, JEROME;
RHEAD, WILLIAM;
KANIS, ADAM B.;
HALL, BRYAN D.

Publication type:

Article

Current awareness in prenatal diagnosis.

Published in:: Prenatal Diagnosis, 1996, v. 16, n. 2, p. 185, doi. 10.1002/pd.1970160217
Publication type:: Article

PK MONDOR: PRENATAL DIAGNOSIS OF A FRAMESHIFT MUTATION IN THE LR PYRUVATE KINASE GENE ASSOCIATED WITH SEVERE HEREDITARY NON-SPHEROCYTIC HAEMOLYTIC ANAEMIA.

Published in:

Prenatal Diagnosis, 1996, v. 16, n. 2, p. 97, doi. 10.1002/(SICI)1097-0223(199602)16:2<97::AID-PD814>3.0.CO;2-O

By:

ROUGER, H.;
GIRODON, E.;
GOOSSENS, M.;
GALACTÉROS, F.;
COHEN-SOLAL, M.

Publication type:

Article

PRENATAL SCREENING FOR DOWN'S SYNDROME USING INHIBIN-A AS A SERUM MARKER.

Published in:

Prenatal Diagnosis, 1996, v. 16, n. 2, p. 143, doi. 10.1002/(SICI)1097-0223(199602)16:2<143::AID-PD825>3.0.CO;2-F

By:

WALD, NICHOLAS J.;
DENSEM, JAMES W.;
GEORGE, LYNNE;
MUTTUKRISHNA, SHAUTHI;
KNIGHT, PHILIP G.

Publication type:

Article

PRENATAL CYTOGENETIC RESULTS FROM CASES REFERRED FOR 44 DIFFERENT TYPES OF ABNORMAL ULTRASOUND FINDINGS.

Published in:

Prenatal Diagnosis, 1996, v. 16, n. 2, p. 109, doi. 10.1002/(SICI)1097-0223(199602)16:2<109::AID-PD818>3.0.CO;2-D

By:

SANFORD HANNA, JULIE;
NEU, RICHARD L.;
LOCKWOOD, DAVID H.

Publication type:

Article

PRENATAL DIAGNOSIS OF MITOCHONDRIAL FATTY ACID OXIDATION DEFECTS.

Published in:

Prenatal Diagnosis, 1996, v. 16, n. 2, p. 117, doi. 10.1002/(SICI)1097-0223(199602)16:2<117::AID-PD820>3.0.CO;2-Z

By:

NADA, MOHAMED A.;
VIANEY-SABAN, CHRISTINE;
ROE, CHARLES R.;
DING, JIA-HUAN;
MATHIEU, MONIQUE;
WAPPNER, REBECCA S.;
BIALER, MARTIN G.;
MCGLYNN, JULIE A.;
MANDON, GINETTE

Publication type:

Article

Masthead.

Published in:: Prenatal Diagnosis, 1996, v. 16, n. 2, p. fmi, doi. 10.1002/pd.1970160201
Publication type:: Article

DISTRIBUTION OF ABNORMAL KARYOTYPES AMONG MALFORMED FETUSES DETECTED BY ULTRASOUND THROUGHOUT GESTATION.

Published in:

Prenatal Diagnosis, 1996, v. 16, n. 2, p. 159, doi. 10.1002/(SICI)1097-0223(199602)16:2<159::AID-PD831>3.0.CO;2-H

By:

RIZZO, NICOLA;
PITTALIS, MARIA CARLA;
PILU, GIANLUIGI;
PEROLO, ANTONELLA;
BANZI, CRISTINA;
VISENTIN, ANTONELLA;
BOVICELLI, LUCIANO

Publication type:

Article

CYTOGENETIC ANALYSIS OF FETAL CHONDROCYTES: A COMPARATIVE STUDY.

Published in:

Prenatal Diagnosis, 1996, v. 16, n. 2, p. 165, doi. 10.1002/(SICI)1097-0223(199602)16:2<165::AID-PD813>3.0.CO;2-E

By:

GELMAN-KOHAN, Z.;
ROSENSAFT, J.;
BEN-HUR, H.;
HABER, A.;
CHEMKE, J.

Publication type:

Article

PRENATAL DIAGNOSIS OF GLYCOGEN STORAGE DISEASE TYPE 1a BY DIRECT MUTATION DETECTION.

Published in:

Prenatal Diagnosis, 1996, v. 16, n. 2, p. 105, doi. 10.1002/(SICI)1097-0223(199602)16:2<105::AID-PD817>3.0.CO;2-K

By:

WONG, LEE-JUN C.

Publication type:

Article