Author:
Chen Chih-Ping,Ko Tsang-Ming,Huang Jian-Pei,Chern Schu-Rern,Wu Peih-Shan,Chen Shin-Wen,Wu Fang-Tzu,Chen Wen-Lin,Lee Meng-Shan,Wang Wayseen
Funder
Ministry of Science and Technology
MacKay Memorial Hospital
Subject
Obstetrics and Gynaecology
Reference17 articles.
1. Familial transmission of recurrent 15q11.2 (BP1-BP2) microdeletion encompassing NIPA1, NIPA2, CYFIP1, and TUBGCP5 associated with phenotypic variability in developmental, speech, and motor delay;Chen;Taiwan J Obstet Gynecol,2017
2. Prenatal diagnosis of a familial 15q11.2 (BP1-BP2) microdeletion encompassing TUBGCP5, CYFIP1, NIPA2 and NIPA1 in a fetus with ventriculomegaly, microcephaly and intrauterine growth restriction on prenatal ultrasound;Chen;Taiwan J Obstet Gynecol,2018
3. Form of 15q proximal duplication appears to be a normal euchromatic variant;Jalal;Am J Med Genet,1994
4. Organisation of the pericentromeric region of chromosome 15: at least four partial gene copies are amplified in patients with a proximal duplication of 15q;Fantes;J Med Genet,2002
5. A cosegregating microduplication of chromosome 15q11.2 pinpoints two risk genes for autism spectrum disorder;van der Zwaag;Am J Med Genet B,2010