Application of array-comparative genomic hybridization in tetralogy of Fallot.
Liu, Lin; Wang, Hong-Dan; Cui, Cun-Ying; Wu, Dong; Li, Tao; Fan, Tai-Bing; Peng, Bang-Tian; Zhang, Lian-Zhong; Wang, Cheng-Zeng.
; 95(49): e5552, 2016 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-27930557
Extensive genetic variation in somatic human tissues.
Prenatal Array Comparative Genomic Hybridization in Fetuses With Structural Cardiac Anomalies.
Chromosomal analysis in IVF: just how useful is it?
A familial interstitial 4q35 deletion with no discernible clinical effects.
A Novel Recurrent Breakpoint Responsible for Rearrangements in the Williams-Beuren Region.
rCGH: a comprehensive array-based genomic profile platform for precision medicine.
[Comparative results of preimplantation genetic screening by array comparative genomic hybridization and new-generation sequencing].
[Prenatal diagnosis and genetic analysis of a fetus with 6q27 microdeletion].
Clinical and molecular cytogenetic analyses of four families with 1q21.1 microdeletion or microduplication.
Prenatal diagnosis and molecular cytogenetic characterization of a de novo 4.858-Mb microdeletion in 15q14 associated with ACTC1 and MEIS2 haploinsufficiency and tetralogy of Fallot.