10p11.2 to 10q11.2 is a yet unreported region leading to unbalanced chromosomal abnormalities without phenotypic consequences-Reference-Cited by-同舟云学术

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10p11.2 to 10q11.2 is a yet unreported region leading to unbalanced chromosomal abnormalities without phenotypic consequences

Published:2009 Issue:1 Volume:124 Page:102-105
ISSN:1424-8581
Container-title:Cytogenetic and Genome Research
language:en
Short-container-title:Cytogenet Genome Res

Author:

Liehr T.,Stumm M.,Wegner R.D.,Bhatt S.,Hickmann P.,Patsalis P.C.,Meins M.,Morlot S.,Klaschka V.,Ewers E.,Hinreiner S.,Mrasek K.,Kosyakova N.,Cai W.W.,Cheung S.W.,Weise A.

Publisher

S. Karger AG

Subject

Genetics (clinical),Genetics,Molecular Biology

Cited by 17 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. Molecular cytogenetic characteristics of small supernumerary marker chromosomes 15 and 22 in asymptomatic carriers;Bulletin of Russian State Medical University;2024-01

3. Molekulyarno-citogeneticheskaya harakteristika malyh sverhchislennyh markernyh hromosom 15 i 22 u asimptomaticheskih nositelej;Вестник Российского государственного медицинского университета;2023-01

4. Prenatal diagnosis and genetic counseling of an inherited unbalanced chromosome abnormalities in a Chinese family;Molecular Cytogenetics;2022-08-15

5. Prenatal diagnosis and genetic counseling of a 10p11.23q11.21 duplication associated with normal phenotype;Molecular Cytogenetics;2022-06-03

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