Renatal diagnosis of mosaic tetrasomy 12p/trisomy 12p by fluorescentin situ hybridization in amniotic fluid cells: A case report of pallister–killian syndrome-Reference-Cited by-同舟云学术

Renatal diagnosis of mosaic tetrasomy 12p/trisomy 12p by fluorescentin situ hybridization in amniotic fluid cells: A case report of pallister–killian syndrome

Published:1995-12 Issue:12 Volume:15 Page:1155-1159
ISSN:0197-3851
Container-title:Prenatal Diagnosis
language:en
Short-container-title:Prenat. Diagn.

Author:

Los Frans J.,Van Opstal Diane,Schol Martin P.,Gaillard Johannes L. J.,Brandenburg Helen,Van Den Ouweland Ans M. W.,In 'T Veld Peter A.

Publisher

Wiley

Subject

Genetics (clinical),Obstetrics and Gynecology

Reference23 articles.

1. Prenatal diagnosis of the Pallister-Killian mosaic aneuploidy syndrome by CVS

2. Double translocation t(7;12),t(2;6) heterozygosity in one family

3. Prenatal diagnosis of tetrasomy 12p byin situ hybridization: Varying levels of mosaicism in different fetal tissues

4. Pallister Killian-mosaic tetrasomy 12 p syndrome. Another prenatally diagnosed case

5. Anthropometric measurements in the second trimester fetus

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