Familial Translocation t(6;20)(p21;p13) Resulting in Partial Trisomy 6p and Partial Monosomy 20p: Report of a New Case and Review of the Literature
Author:
Publisher
S. Karger AG
Subject
Genetics(clinical),Genetics,Molecular Biology
Reference6 articles.
1. Alagille syndrome and deletion of 20p.
2. Partial trisomy 6p due to familial translocation t(6;20)(p21;p13)
3. A tale of two deletions: A report of two novel 20p13 → pter deletions
4. Aneuploid and unbalanced sperm in two translocation carriers: evaluation of the genetic risk
Cited by 3 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. De novo t(1;6)(p13p21.3) Dengeli Resiprokal Translokasyonun İnfertilite ile İlişkisi;Düzce Üniversitesi Sağlık Bilimleri Enstitüsü Dergisi;2020-01-31
2. Renal complications in 6p duplication syndrome: Microarray-based investigation of the candidate gene(s) for the development of congenital anomalies of the kidney and urinary tract (CAKUT) and focal segmental glomerular sclerosis (FSGS);American Journal of Medical Genetics Part A;2015-02-18
3. Karyotype-Phenotype Correlation in Partial Trisomies of the Short Arm of Chromosome 6: A Family Case Report and Review of the Literature;Cytogenetic and Genome Research;2013
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