22q11.2 deletions in a series of patients with non-selective congenital heart defects: incidence, type of defects and parental origin-Reference-Cited by-同舟云学术

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22q11.2 deletions in a series of patients with non-selective congenital heart defects: incidence, type of defects and parental origin

Published:1998-01 Issue:1 Volume:53 Page:63-69
ISSN:0009-9163
Container-title:Clinical Genetics
language:en
Short-container-title:Clin Genet

Author:

Fokstuen S,Arbenz U,Artan S,Dutly F,Bauersfeld U,Brecevic L,Fasnacht M,Rathlisberger B,Schinzel A

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Cited by 62 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Sex-specific recombination patterns predict parent of origin for recurrent genomic disorders;BMC Medical Genomics;2021-06-09

2. CNVs in the 22q11.2 Chromosomal Region Should Be an Early Suspect in Infants with Congenital Cardiac Disease;Clinical Medicine Insights: Cardiology;2021-01

3. Congenital Heart Defects and Dysmorphic Facial Features in Patients Suspicious of 22q11.2 Deletion Syndrome in Southern Brazil;Journal of Pediatric Genetics;2020-06-17

4. Ontogeny of the facial phenotypic variability in Mexican patients with 22q11.2 deletion syndrome;Head & Face Medicine;2019-12

5. The 22q11.2 Microdeletion in Pediatric Patients with Cleft Lip, Palate, or Both and Congenital Heart Disease: A Systematic Review;Journal of Pediatric Genetics;2019-10-23

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