Prenatal diagnosis of de novo interstitial deletions involving 5q23.1–q23.3 and 18q12.1–q12.3 by array CGH using uncultured amniocytes in a pregnancy with fetal interrupted aortic arch and atrial septal defect-Reference-Cited by-同舟云学术

Prenatal diagnosis of de novo interstitial deletions involving 5q23.1–q23.3 and 18q12.1–q12.3 by array CGH using uncultured amniocytes in a pregnancy with fetal interrupted aortic arch and atrial septal defect

Published:2013-12 Issue:2 Volume:531 Page:496-501
ISSN:0378-1119
Container-title:Gene
language:en
Short-container-title:Gene

Author:

Chen Chih-Ping,Huang Ming-Chao,Chen Yi-Yung,Chern Schu-Rern,Wu Peih-Shan,Chen Yu-Ting,Su Jun-Wei,Wang Wayseen

Funder

National Science Council

Mackay Memorial Hospital, Taipei, Taiwan

Publisher

Elsevier BV

Subject

Genetics,General Medicine

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4. FBN2 mutations in congenital contractural arachnodactyly (CCA);Carmical;Am. J. Hum. Genet.,2000

5. Fibrillins 1 and 2 perform partially overlapping functions during aortic development;Carta;J. Biol. Chem.,2006

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5. Prenatal diagnosis and molecular cytogenetic characterization of an interstitial deletion of 18q12.1-q12.3 encompassing DTNA , CELF4 and SETBP1;Taiwanese Journal of Obstetrics and Gynecology;2017-12