Duplication deficiency as the result of meiotic segregation of a maternal InV (10)
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics (clinical),Genetics
Link
http://link.springer.com/content/pdf/10.1007/BF00271171.pdf
Cited by 12 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 molecular cytogenetic characterization of rec(10)dup(10p)inv(10)(p11.2q26.3) in a fetus associated with paternal pericentric inversion;Taiwanese Journal of Obstetrics and Gynecology;2016-10
2. An unusual de novo duplication 10p/deletion 10q syndrome: The first case in Korea;Journal of Genetic Medicine;2015-06-30
3. Relatives with Opposite Chromosome Constitutions, rec(10)dup(10p)inv(10)(p15.1q26.12) and rec(10)dup(10q)inv(10)(p15.1q26.12), due to a Familial Pericentric Inversion;Cytogenetic and Genome Research;2014
4. First small supernumerary ring chromosome carrying 10q euchromatin in a patient with mild phenotype characterized by molecular cytogenetic techniques and review of the literature;Cytogenetic and Genome Research;2004-12-13
5. Case report of rec(7)dup(7q)inv(7)(p22q22) and a review of the recombinants resulting from parental pericentric inversions on any chromosomes;American Journal of Medical Genetics;1997-12-19
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