Prenatal diagnosis and molecular cytogenetic characterization of a chromosome 1q42.3-q44 deletion in a fetus associated with ventriculomegaly on prenatal ultrasound

Author:

Chen Chih-Ping,Ko Tsang-Ming,Wang Liang-Kai,Chern Schu-Rern,Wu Peih-Shan,Chen Shin-Wen,Wu Fang-Tzu,Chen Yun-Yi,Chen Wen-Lin,Wang Wayseen

Funder

Ministry of Science and Technology, Taiwan

MacKay Memorial Hospital, Taipei, Taiwan

Publisher

Elsevier BV

Subject

Obstetrics and Gynaecology

Reference36 articles.

1. Toward clinical and molecular understanding of pathogenic variants in the ZBTB18 gene;van der Schoot;Mol Genet Genomic Med,2018

2. High-resolution array CGH defines critical regions and candidate genes for microcephaly, abnormalities of the corpus callosum, and seizure phenotypes in patients with microdeletions of 1q43q44;Ballif;Hum Genet,2012

3. Prenatal diagnosis of a fetus with terminal deletion of chromosome 1 (q41);Rotmensch;Prenat Diagn,1991

4. Prenatal diagnosis of terminal deletion 1 (q42);Dallapiccola;Prenat Diagn,1992

5. Prenatal diagnosis of partial monosomy 1q (1q42.3→qter) associated with hydrocephalus and corpus callosum agenesis;Chen;Genet Counsel,2010

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