Molecular genetic characterization of a prenatally detected de novo interstitial deletion of chromosome 20p (20p12-p13) encompassing JAG1 and a literature review of prenatal diagnosis of Alagille syndrome-Reference-Cited by-同舟云学术

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Molecular genetic characterization of a prenatally detected de novo interstitial deletion of chromosome 20p (20p12-p13) encompassing JAG1 and a literature review of prenatal diagnosis of Alagille syndrome

Published:2017-06 Issue:3 Volume:56 Page:390-393
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,Yin Chang-Sheng,Wang Liang-Kai,Chern Schu-Rern,Chen Shin-Wen,Lai Shih-Ting,Wu Peih-Shan,Chen Wen-Lin,Wang Wayseen

Funder

Ministry of Science and Technology

MacKay Memorial Hospital, Taipei, Taiwan

Publisher

Elsevier BV

Subject

Obstetrics and Gynecology

Reference15 articles.

1. Alagille syndrome;Spinner,1993

2. Alagille syndrome: clinical perspectives;Saleh;Appl Clin Genet,2016

3. Deletions of 20p12 in Alagille syndrome: frequency and molecular characterization;Krantz;Am J Med Genet,1997

4. Exon 6 of human Jagged-1 encodes an autonomously folding unit;Guarnaccia;FEBS Lett,2004

5. Prenatal diagnosis and array comparative genomic hybridization characterization of a de novo interstitial deletion of chromosome 20p;Chen;Taiwan J Obstet Gynecol,2011

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