A Subtle Familial Translocation t(3;21)(p26.3;q22.3): An Apparently Healthy Boy with a 3p Deletion and 21q Duplication-Reference-Cited by-同舟云学术

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A Subtle Familial Translocation t(3;21)(p26.3;q22.3): An Apparently Healthy Boy with a 3p Deletion and 21q Duplication

Published:2010 Issue:4 Volume:128 Page:245-249
ISSN:1424-8581
Container-title:Cytogenetic and Genome Research
language:en
Short-container-title:Cytogenet Genome Res

Author:

Gijsbers A.C.J.,van Haeringen A.,Bosch C.A.J.,Hansson K.,Verschuren M.,Bakker E.,Breuning M.H.,Ruivenkamp C.A.L.

Publisher

S. Karger AG

Subject

Genetics(clinical),Genetics,Molecular Biology

Cited by 10 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. Neuronal migration genes and a familial translocation t (3;17): candidate genes implicated in the phenotype;BMC Medical Genetics;2020-02-06

2. Autism spectrum disorder, anxiety and severe depression in a male patient with deletion and duplication in the 21q22.3 region: A case report;Biomedical Reports;2019-05-13

3. Down syndrome phenotype in a boy with a mosaic microduplication of chromosome 21q22;Molecular Cytogenetics;2018-12

4. Systematic reanalysis of partial trisomy 21 cases with or without Down syndrome suggests a small region on 21q22.13 as critical to the phenotype;Human Molecular Genetics;2016-04-22

5. Prenatal diagnosis and molecular cytogenetic characterization of de novo partial monosomy 3p (3p26.3→pter) and partial trisomy 16q (16q23.1→qter);Taiwanese Journal of Obstetrics and Gynecology;2016-04

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