Prenatal diagnosis of familial transmission of 17q12 microduplication associated with no apparent phenotypic abnormality

Author:

Chen Chih-Ping,Fu Chung-Hu,Lin Yi-Hui,Chern Schu-Rern,Wu Peih-Shan,Chen Yen-Ni,Chen Shin-Wen,Wang Wayseen

Funder

Ministry of Science and Technology

MacKay Memorial Hospital, Taipei, Taiwan

Publisher

Elsevier BV

Subject

Obstetrics and Gynaecology

Reference17 articles.

1. Detection of recurrent transmission of 17q12 microdeletion by array comparative genomic hybridization in a fetus with prenatally diagnosed hydronephrosis, hydroureter and multicystic kidney, and variable clinical spectrum in the family;Chen;Taiwan J Obstet Gynecol,2013

2. Prenatal diagnosis of 17q12 duplication and deletion syndrome in two fetuses with congenital anomalies;Li;Taiwan J Obstet Gynecol,2014

3. Mefford H, Mitchell E, Hodge J. 17q12 recurrent duplication. In: Pagon RA, Adam MP, Ardinger HH, Wallace SE, Amemiya A, Bean LJH, et al, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington; 1993–2016. Available at: http://www.ncbi.nlm.nih.gov/pubmed/26925472. [accessed 02.08.16].

4. Two members of an HNF1 homeoprotein family are expressed in human liver;Bach;Nucl Acids Res,1991

5. Requirement for Lim1 in head-organizer function;Shawlot;Nature,1995

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