The discovery of microdeletion syndromes in the post-genomic era: review of the methodology and characterization of a new 1q41q42 microdeletion syndrome-Reference-Cited by-同舟云学术

The discovery of microdeletion syndromes in the post-genomic era: review of the methodology and characterization of a new 1q41q42 microdeletion syndrome

Published:2007-09 Issue:9 Volume:9 Page:607-616
ISSN:1098-3600
Container-title:Genetics in Medicine
language:en
Short-container-title:Genetics in Medicine

Author:

Shaffer Lisa G.,Theisen Aaron,Bejjani Bassem A.,Ballif Blake C.,Aylsworth Arthur S.,Lim Cynthia,McDonald Marie,Ellison Jay W.,Kostiner Dana,Saitta Sulagna,Shaikh Tamim

Publisher

Elsevier BV

Subject

Genetics (clinical)

Reference70 articles.

1. Supravalvular aortic stenosis: a complex syndrome with and without mental retardation;Beuren;Birth Defects Orig Artic Ser,1972

2. Familial 15q12 duplication associated with Williams phenotype;Miles;Am J Hum Genet,1983

Cited by 143 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. Prenatal Ultrasound Diagnosis of Congenital Diaphragmatic Hernia in a Fetus With Fryns “Anophthalmia-Plus” Syndrome: A Case Report;Cureus;2024-08-28

2. G protein-coupled estrogen receptor 1 deficiency impairs adult hippocampal neurogenesis in mice with schizophrenia;Journal of Chemical Neuroanatomy;2023-10

3. High Performance of a Dominant/X-Linked Gene Panel in Patients with Neurodevelopmental Disorders;Genes;2023-03-13

4. Sushi domain-containing protein 4 binds to epithelial growth factor receptor and initiates autophagy in an EGFR phosphorylation independent manner;Journal of Experimental & Clinical Cancer Research;2022-12-29

5. Molecular Mechanisms Contributing to the Etiology of Congenital Diaphragmatic Hernia: A Review and Novel Cases;The Journal of Pediatrics;2022-07