Proximal 10q duplication in a child with severe central hypotonia characterized by array-comparative genomic hybridization: A case report and review of the literature-Reference-Cited by-同舟云学术

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Proximal 10q duplication in a child with severe central hypotonia characterized by array-comparative genomic hybridization: A case report and review of the literature

Published:2014-02-06 Issue:4 Volume:7 Page:953-957
ISSN:1792-0981
Container-title:Experimental and Therapeutic Medicine
language:en
Short-container-title:

Author:

MANOLAKOS EMMANOUIL,VETRO ANNALISA,GARAS ANTONIOS,THOMAIDIS LORETTA,KEFALAS KONSTANTINOS,KITSOS GEORGE,ZIEGLER MONIKA,LIEHR THOMAS,ZUFFARDI ORSETTA,PAPOULIDIS IOANNIS

Publisher

Spandidos Publications

Subject

Cancer Research,Immunology and Microbiology (miscellaneous),General Medicine

Cited by 6 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 diagnosis and genetic counseling of a de novo 10q11.21q11.23 duplication associated with a normal phenotype;Journal of International Medical Research;2024-08

2. The clinical diagnostic utility of array cgh in children with syndromic microcephaly;Annals of Indian Academy of Neurology;2022

3. Prenatal exome sequencing and chromosomal microarray analysis in fetal structural anomalies in a highly consanguineous population reveals a propensity of ciliopathy genes causing multisystem phenotypes;Human Genetics;2021-12-01

4. Clinical Characterization of a 6-Year-Old Patient with Autism and Two Adjacent Duplications on 10q11.22q11.23. A Case Report;Children;2021-06-18

5. Recurrent Rare Copy Number Variants Increase Risk for Esotropia;Investigative Opthalmology & Visual Science;2020-08-11

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