17p13.3 Microdeletion: Insights on Genotype-Phenotype Correlation-Reference-Cited by-同舟云学术

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17p13.3 Microdeletion: Insights on Genotype-Phenotype Correlation

Published:2016-11-25 Issue:1 Volume:8 Page:36-41
ISSN:1661-8769
Container-title:Molecular Syndromology
language:en
Short-container-title:Mol Syndromol

Author:

Barros Fontes Marshall I.,dos Santos Ana P.,Rossi Torres Fábio,Lopes-Cendes Iscia,Cendes Fernando,Appenzeller Simone,Kawasaki de Araujo Tânia,Lopes Monlleó Isabella,Gil-da-Silva-Lopes Vera L.

Publisher

S. Karger AG

Subject

Genetics (clinical),Genetics

Cited by 16 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. Crk and Crkl Are Required in the Endocardial Lineage for Heart Valve Development;Journal of the American Heart Association;2023-09-19

2. Clinical findings and genetic analysis of patients with copy number variants involving 17p13.3 using a single nucleotide polymorphism array: a single-center experience;BMC Medical Genomics;2022-12-21

3. Further expansion and confirmation of phenotype in rare loss of YWHAE gene distinct from Miller–Dieker syndrome;American Journal of Medical Genetics Part A;2022-11-25

4. Prenatal diagnosis of Miller-Dieker syndrome/PAFAH1B1-related lissencephaly: Ultrasonography and genetically investigative results;European Journal of Obstetrics & Gynecology and Reproductive Biology;2022-07

5. Case Report: First Case of Non-restrictive Ventricular Septal Defect With Congestive Heart Failure in a Chinese Han Male Infant Carrying a Class II Chromosome 17p13.3 Microduplication;Frontiers in Pediatrics;2022-02-28

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