Works matching IS 01973851 AND DT 1999 AND VI 19 AND IP 10

Results: 22

Fetal cells in maternal blood: NIFTY clinical trial interim analysis.

Published in:

Prenatal Diagnosis, 1999, v. 19, n. 10, p. 994, doi. 10.1002/(SICI)1097-0223(199910)19:10<994::AID-PD662>3.0.CO;2-H

By:

Bianchi, Diana W.;
Simpson, Joe Leigh;
Jackson, Laird G.;
Evans, Mark I.;
Elias, Sherman;
Holzgreve, Wolfgang;
Sullivan, Lisa M.;
de la Cruz, Felix

Publication type:

Article

Sonographic diagnosis of limb reduction defects in a fetus with haemoglobin Bart's disease at 12 weeks of gestation.

Published in:

Prenatal Diagnosis, 1999, v. 19, n. 10, p. 983, doi. 10.1002/(SICI)1097-0223(199910)19:10<983::AID-PD671>3.0.CO;2-N

By:

Lam, Yung Hang;
Tang, Mary Hoi Yin

Publication type:

Article

Prenatal diagnosis of lysosomal storage diseases using fetal blood.

Published in:

Prenatal Diagnosis, 1999, v. 19, n. 10, p. 930, doi. 10.1002/(SICI)1097-0223(199910)19:10<930::AID-PD664>3.0.CO;2-X

By:

Groener, Johanna E. M.;
de Graaf, Frank L.;
Poorthuis, Ben J. H. M.;
Kanhai, Humphrey H. H.

Publication type:

Article

Maternal urine hyperglycosylated hCG in pregnancies with Down syndrome.

Published in:

Prenatal Diagnosis, 1999, v. 19, n. 10, p. 918, doi. 10.1002/(SICI)1097-0223(199910)19:10<918::AID-PD680>3.0.CO;2-4

By:

Cuckle, H. S.;
Shahabi, S.;
Sehmi, I. K.;
Jones, R.;
Cole, L. A.

Publication type:

Article

Prenatal diagnosis on fetal cells obtained from maternal peripheral blood: Report of 66 cases.

Published in:

Prenatal Diagnosis, 1999, v. 19, n. 10, p. 934, doi. 10.1002/(SICI)1097-0223(199910)19:10<934::AID-PD675>3.0.CO;2-P

By:

Rodríguez de Alba, M.;
Palomino, P.;
Jurado, A.;
Sanz, R.;
Ibañez, M. A.;
Fernández-Moya, J. M.;
Ayuso, C.;
Díaz-Recasens, J.;
Lahoz, C.;
Ramos, C.

Publication type:

Article

Fetal muscle biopsy as a diagnostic tool in Duchenne muscular dystrophy.

Published in:

Prenatal Diagnosis, 1999, v. 19, n. 10, p. 921, doi. 10.1002/(SICI)1097-0223(199910)19:10<921::AID-PD660>3.0.CO;2-A

By:

Nevo, Yoram;
Shomrat, Ruth;
Yaron, Yuval;
Orr-Urtreger, Avi;
Harel, Shaul;
Legum, Cyril

Publication type:

Article

Nuchal translucency and trisomy 18.

Published in:

Prenatal Diagnosis, 1999, v. 19, n. 10, p. 995, doi. 10.1002/(SICI)1097-0223(199910)19:10<995::AID-PD673>3.0.CO;2-C

By:

Wald, Nicholas J.;
Hackshaw, Allan K.;
Watt, Hilary

Publication type:

Article

Accuracy of the haemoglobin alkaline denaturation test for detecting maternal blood contamination of fetal blood samples for prenatal karyotyping.

Published in:

Prenatal Diagnosis, 1999, v. 19, n. 10, p. 927, doi. 10.1002/(SICI)1097-0223(199910)19:10<927::AID-PD668>3.0.CO;2-H

By:

Sepulveda, Waldo;
Be, Cecilia;
Youlton, Ronald;
Gutierrez, Jorge;
Carstens, Eduardo

Publication type:

Article

A retrospective evaluation of second-trimester serum screening for fetal trisomy 18: experience of two laboratories.

Published in:

Prenatal Diagnosis, 1999, v. 19, n. 10, p. 947, doi. 10.1002/(SICI)1097-0223(199910)19:10<947::AID-PD674>3.0.CO;2-M

By:

Sancken, U.;
Bartels, I.;
Louwen, F.;
Eiben, B.

Publication type:

Article

Fetus with long QT syndrome manifested by tachyarrhythmia: a case report.

Published in:

Prenatal Diagnosis, 1999, v. 19, n. 10, p. 990, doi. 10.1002/(SICI)1097-0223(199910)19:10<990::AID-PD679>3.0.CO;2-#

By:

Ohkuchi, Akihide;
Shiraishi, Hirohiko;
Minakami, Hisanori;
Eguchi, Yukari;
Izumi, Akio;
Sato, Ikuo

Publication type:

Article

Cloning of multiple keratin 16 genes facilitates prenatal diagnosis of pachyonychia congenita type 1.

Published in:

Prenatal Diagnosis, 1999, v. 19, n. 10, p. 941, doi. 10.1002/(SICI)1097-0223(199910)19:10<941::AID-PD663>3.0.CO;2-W

By:

Smith, Frances J. D.;
McKusick, Victor A.;
Nielsen, Karl;
Pfendner, Ellen;
Uitto, Jouni;
McLean, W. H. Irwin

Publication type:

Article

Elevated second-trimester maternal serum hCG in patients undergoing haemodialysis.

Published in:

Prenatal Diagnosis, 1999, v. 19, n. 10, p. 955, doi. 10.1002/(SICI)1097-0223(199910)19:10<955::AID-PD670>3.0.CO;2-X

By:

Cheng, Po-Jen;
Liu, Ching-Ming;
Chang, Shuenn-Dyh;
Lin, Yu-Ting;
Soong, Yung-Kwei

Publication type:

Article

Collaborative study of maternal urine β -core human chorionic gonadotrophin screening for Down syndrome.

Published in:

Prenatal Diagnosis, 1999, v. 19, n. 10, p. 911, doi. 10.1002/(SICI)1097-0223(199910)19:10<911::AID-PD666>3.0.CO;2-W

By:

Cuckle, Howard S.;
Canick, Jacob A.;
Kellner, Leonard H.

Publication type:

Article

Preconceptional use of folic acid amongst women of advanced maternal age.

Published in:

Prenatal Diagnosis, 1999, v. 19, n. 10, p. 996, doi. 10.1002/(SICI)1097-0223(199910)19:10<996::AID-PD677>3.0.CO;2-#

By:

de Walle, H. E. K.;
Cornel, M. C.;
de Smit, D. J.;
de Jong-van den Berg, L. T. W.

Publication type:

Article

The cardiac echogenic focus.

Published in:

Prenatal Diagnosis, 1999, v. 19, n. 10, p. 972, doi. 10.1002/(SICI)1097-0223(199910)19:10<972::AID-PD650>3.0.CO;2-W

By:

Simpson, John

Publication type:

Article

Prenatal diagnosis of Sanfilippo type A syndrome in a family with S66W mutant allele.

Published in:

Prenatal Diagnosis, 1999, v. 19, n. 10, p. 993, doi. 10.1002/(SICI)1097-0223(199910)19:10<993::AID-PD661>3.0.CO;2-L

By:

Di Natale, Paola;
Villani, Guglielmo R. D.;
Esposito, Sabrina;
Balzano, Nicola;
Filocamo, Mirella;
Gatti, Rosanna

Publication type:

Article

Prenatal diagnosis of partial trisomy 3p(3p23→pter) and monosomy 7q(7q36→qter) in a fetus with microcephaly alobar holoprosencephaly and cyclopia.

Published in:

Prenatal Diagnosis, 1999, v. 19, n. 10, p. 986, doi. 10.1002/(SICI)1097-0223(199910)19:10<986::AID-PD672>3.0.CO;2-H

By:

Chen, Chih-Ping;
Devriendt, Koenraad;
Lee, Chen-Chi;
Chen, Wen-Lin;
Wang, Wayseen;
Wang, Tao-Yeuan

Publication type:

Article

Non-lethal arthrogryposis multiplex congenita presenting with cystic hygroma at 13 weeks gestational age.

Published in:

Prenatal Diagnosis, 1999, v. 19, n. 10, p. 966, doi. 10.1002/(SICI)1097-0223(199910)19:10<966::AID-PD683>3.0.CO;2-J

By:

Scott, Heather;
Hunter, Alasdair;
Bédard, Brigit

Publication type:

Article

Prenatal diagnosis of mosaicism for partial trisomy 8: a case report including fetal pathology.

Published in:

Prenatal Diagnosis, 1999, v. 19, n. 10, p. 976, doi. 10.1002/(SICI)1097-0223(199910)19:10<976::AID-PD665>3.0.CO;2-C

By:

Jay, A.;
Kilby, M. D.;
Roberts, E.;
Brackley, K.;
Platt, C.;
McHugo, J.;
Davison, E. V.

Publication type:

Article

Prenatal diagnosis for facioscapulohumeral muscular dystrophy (FSHD).

Published in:

Prenatal Diagnosis, 1999, v. 19, n. 10, p. 959, doi. 10.1002/(SICI)1097-0223(199910)19:10<959::AID-PD676>3.0.CO;2-B

By:

Upadhyaya, Meena;
MacDonald, Moira;
Ravine, David

Publication type:

Article

The proform of eosinophil major basic protein: a new maternal serum marker for Down syndrome.

Published in:

Prenatal Diagnosis, 1999, v. 19, n. 10, p. 905, doi. 10.1002/(SICI)1097-0223(199910)19:10<905::AID-PD658>3.0.CO;2-Q

By:

Christiansen, Michael;
Oxvig, Claus;
Wagner, Jill M.;
Qin, Qiu-Ping;
Nguyen, Tri H.;
Overgaard, Michael T.;
Larsen, Severin O.;
Sottrup-Jensen, Lars;
Gleich, Gerald J.;
Nørgaard-Pedersen, Bent

Publication type:

Article

Transplacental exposure to antipsychotic drugs during pregnancy and megacystis in the fetus.

Published in:

Prenatal Diagnosis, 1999, v. 19, n. 10, p. 980, doi. 10.1002/(SICI)1097-0223(199910)19:10<980::AID-PD669>3.0.CO;2-3

By:

Okuno, Suzuka;
Hamada, Hiromi;
Fujiki, Yutaka;
Yasuoka, Mana;
Watanabe, Hideki;
Yamada, Naoki;
Sohda, Satoshi;
Kubo, Takeshi

Publication type:

Article