» Articles » PMID: 8506232

Trisomy 15 in Chorionic Villi and Prader-Willi Syndrome at Birth

Overview
Journal Prenat Diagn
Publisher Wiley
Date 1993 Apr 1
PMID 8506232
Citations 4
Authors
Affiliations
Soon will be listed here.
Citing Articles

Possibility of early diagnosis in a fetus affected by Prader‑Willi syndrome with maternal hetero‑UPD15: A lesson to be learned.

Dong Y, Liu S, Li J, Li J, Chen Q, Luo J Mol Med Rep. 2019; 20(1):95-102.

PMID: 31115529 PMC: 6580037. DOI: 10.3892/mmr.2019.10246.


Prader-Willi syndrome in a child with mosaic trisomy 15 and mosaic triplo-X: a molecular analysis.

Devriendt K, Matthijs G, Claes S, Legius E, Proesmans W, Cassiman J J Med Genet. 1997; 34(4):318-22.

PMID: 9138157 PMC: 1050920. DOI: 10.1136/jmg.34.4.318.


Distribution of mosaicism in human placentae.

Henderson K, Shaw T, Barrett I, Telenius A, Wilson R, Kalousek D Hum Genet. 1996; 97(5):650-4.

PMID: 8655147 DOI: 10.1007/BF02281877.


Age-related nonrandom chromosomal abnormalities in human low-grade astrocytomas.

Thiel G, Lozanova T, Vogel S, Kintzel D, JANISCH W, WITKOWSKI R Hum Genet. 1993; 91(6):547-50.

PMID: 8340108 DOI: 10.1007/BF00205078.