Terminal deletion of chromosome 10q26 due to a paternal translocation {(7;10)(q36;q26)}
Author:
Publisher
Wiley
Subject
Genetics (clinical)
Reference13 articles.
1. Severe mental retardation in six generations of a large South African family carrying a translocation t(6;10)(q27;q25.2).
2. Terminal deletion of the long arm of chromosome 10: Case report and review of the literature
3. Familial reciprocal translocation, t(2;10)(p24;q26), resulting in duplication 2p and deletion 10q
4. Phenotype associated with ring 10 chromosome: Report of patient and review of literature
Cited by 7 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. Oculofacial Manifestations of Chromosomal Aberrations;The Eye in Pediatric Systemic Disease;2017
2. Deletion of the distal long arm of chromosome 10; is there a characteristic phenotype? A report of 15 de novo and familial cases;American Journal of Medical Genetics;2003-10-29
3. Terminal deletion of chromosome 10q at band 26.1: Follow-up in an adolescent male with high-output renal failure from congenital obstructive uropathy;American Journal of Medical Genetics;1999-09-10
4. Partial monosomy of distal 10q: Three new cases and a review;American Journal of Medical Genetics;1999-09-03
5. Terminal deletion of the long arm of chromosome 10: A new case with breakpoint in q25.3;American Journal of Medical Genetics;1998-04-28
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