The prenatal diagnosis and genetic counseling of chromosomal micro-duplication on 10q24.3 in a fetus

Author:

Lai Shaoyang,Zhang Xueqin,Feng Ling,He Mengzhou,Wang Shaoshuai

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

General Medicine

Reference36 articles.

1. Single-cell analysis of cardiogenesis reveals basis for organ-level developmental defects;de Soysa;Nature,2019

2. Environmental and individual exposure and the risk of congenital anomalies: a review of recent epidemiological evidence;Baldacci;Epidemiol Prev,2018

3. A 0.7 Mb de novo duplication at 7q21;Velinov;3 including the genes DLX5 and DLX6 in a patient with split-hand/split-foot malformation Am J Med Genet A,2012

4. A genomic rearrangement resulting in a tandem duplication is associated with split hand-split foot malformation 3 (SHFM3) at 10q24;de Mollerat;Hum Mol Genet,2003

5. Duplications of BHLHA9 are associated with ectrodactyly and tibia hemimelia inherited in non-Mendelian fashion;Klopocki;J Med Genet,2012

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