Familial 10p trisomy resulting from a maternal pericentric inversion
Author:
Publisher
Wiley
Subject
Genetics(clinical)
Reference38 articles.
1. Trisomy 10p due to a de novo t(10p;13p)
2. Trisomy 10p due to t(5;10)(p15;p11) segregating in a large sibship
3. Increased HK1 activity levels in the red cells of a patient with a de novo trisomy 10p: t(Y;10)(p11;p12)
4. Brother and sister with trisomy 10p
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1. Molecular cytogenetic analysis of partial monosomy 10p and trisomy 10q resulting from familial pericentric inversion (10): a first case report in Chinese population;Molecular Cytogenetics;2022-06-07
2. Novel case of paternal paracentric inversion causing partial trisomy 13 and review of the literature;American Journal of Medical Genetics Part A;2017-04-10
3. Oculofacial Manifestations of Chromosomal Aberrations;The Eye in Pediatric Systemic Disease;2017
4. 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
5. An unusual de novo duplication 10p/deletion 10q syndrome: The first case in Korea;Journal of Genetic Medicine;2015-06-30
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