Inv(10)(p11.2q21.2), a variant chromosome-Reference-Cited by-同舟云学术

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Inv(10)(p11.2q21.2), a variant chromosome

Published:1997-11-17 Issue:2 Volume:101 Page:175-180
ISSN:0340-6717
Container-title:Human Genetics
language:
Short-container-title:Human Genetics

Author:

Collinson M. N.,Fisher Andrew M.,Walker Jean,Currie Jane,Williams Lisa,Roberts Paul

Publisher

Springer Science and Business Media LLC

Subject

Genetics(clinical),Genetics

Link

http://link.springer.com/content/pdf/10.1007/s004390050609.pdf

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. Molecular Cytogenetic Characterization of Rare but Repeatedly Observed Inversions in German Population;Cytogenetic and Genome Research;2024-05-24

2. Higher chromosomal abnormality rate in blastocysts from a subset of patients with pericentric inversion (Inv) 1 variant;Human Fertility;2023-02-20

3. Prenatal Diagnosis of Chromosomal Abnormalities through Chorionic Villus Sampling and Amniocentesis;Genetic Disorders and the Fetus;2021-04-20

4. Fertility problems in males carrying an inversion of chromosome 10;Open Medicine;2021-01-01

5. Follow-up of two adult brothers with homozygous CEP57 pathogenic variants expands the phenotype of Mosaic Variegated Aneuploidy Syndrome;European Journal of Medical Genetics;2020-11

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