Detection of paternal uniparental disomy 9 in a neonate with prenatally detected mosaicism for a small supernumerary marker chromosome 9 and a supernumerary ring chromosome 9-Reference-Cited by-同舟云学术

Detection of paternal uniparental disomy 9 in a neonate with prenatally detected mosaicism for a small supernumerary marker chromosome 9 and a supernumerary ring chromosome 9

Published:2017-08 Issue:4 Volume:56 Page:527-533
ISSN:1028-4559
Container-title:Taiwanese Journal of Obstetrics and Gynecology
language:en
Short-container-title:Taiwanese Journal of Obstetrics and Gynecology

Author:

Chen Chih-Ping,Chen Ming,Wang Liang-Kai,Chern Schu-Rern,Wu Peih-Shan,Chen Shin-Wen,Lai Shih-Ting,Chang Shun-Ping,Yang Chien-Wen,Pan Chen-Wen,Wang Wayseen

Funder

Ministry of Science and Technology

MacKay Memorial Hospital

Publisher

Elsevier BV

Subject

Obstetrics and Gynecology

Reference41 articles.

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2. Small marker chromosomes in man: origin from pericentric heterochromatin of chromosomes 1, 9, and 16;Callen;J Med Genet,1990

3. Molecular cytogenetic and clinical studies of 42 patients with marker chromosomes;Callen;Am J Med Genet,1992

4. Chromosomal origin of de novo marker chromosomes identified prenatally;Miller;Am J Hum Genet,1992

5. Characterization of supernumerary ring marker chromosomes by fluorescence in situ hybridization (FISH);Blennow;Am J Hum Genet,1993

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