Form of 15q proximal duplication appears to be a normal euchromatic variant
Author:
Publisher
Wiley
Subject
Genetics (clinical)
Reference14 articles.
1. Proximal 15q variant with normal phenotype in three unrelated individuals
2. Conference report: First international scientific workshop on Prader-Willi Syndrome and Other Chromosome 15q Deletion Disorders
3. Duplication of chromosome 15 in the region 15q11-13 in a patient with developmental delay and ataxia with similarities to Angelman syndrome.
4. Proximal duplications of chromosome 15: clinical dilemmas
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1. Prenatal diagnosis and genetic counseling of a paternally inherited microduplication 18q11.1 to 18q11.2 in a chinese family;Molecular Cytogenetics;2022-09-01
2. Prenatal diagnosis and genetic counseling of a paternally inherited microduplication 18q11.1 to 18q11.2 in a Chinese family;2022-08-17
3. Familial microdeletion 18p11.32 to 18p11.31 in a Chinese family with normal phenotype;Molecular Cytogenetics;2022-03-24
4. Prenatal diagnosis of a familial normal euchromatic variant of dup(15)(q11.2q11.2) in a pregnancy with a favorable outcome;Taiwanese Journal of Obstetrics and Gynecology;2020-09
5. Chromosome Heteromorphism (Summaries);Human Chromosome Variation: Heteromorphism, Polymorphism and Pathogenesis;2017
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