An Interstitial 4q31.21q31.22 Microdeletion Associated with Developmental Delay: Case Report and Literature Review-Reference-Cited by-同舟云学术

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An Interstitial 4q31.21q31.22 Microdeletion Associated with Developmental Delay: Case Report and Literature Review

Published:2014 Issue:4 Volume:142 Page:227-238
ISSN:1424-8581
Container-title:Cytogenetic and Genome Research
language:en
Short-container-title:Cytogenet Genome Res

Author:

Vlaikou Angeliki-Maria,Manolakos Emmanouil,Noutsopoulos Dimitrios,Markopoulos Georgios,Liehr Thomas,Vetro Annalisa,Ziegler Monika,Weise Anja,Kreskowski Katharina,Papoulidis Ioannis,Thomaidis Loretta,Syrrou Maria

Publisher

S. Karger AG

Subject

Genetics (clinical),Genetics,Molecular Biology

Cited by 9 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. Copy number variants at 4q31.3 affecting the regulatory region of FBXW7 associated with neurodevelopmental delay;Clinical Genetics;2024-05-23

2. A Novel Psychiatric Phenotype of Chromosome 4q Deletion: A case report;2023-09-22

3. Sequence Motif Analysis of PRDM9 and Short Inverted Repeats Suggests Their Contribution to Human Microdeletion and Microduplication Syndromes;BioMedInformatics;2023-04-01

4. Prenatal Diagnosis of Combined Maternal 4q Interstitial Deletion and Paternal 15q Microduplication;Genes;2021-10-16

5. Prenatal diagnosis of a maternal 7.22-Mb deletion at chromosome 4q32.2q32.3 by SNP array;Molecular Cytogenetics;2020-04-10

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