Trisomy 10 mosaicism and maternal uniparental disomy 10 in a liveborn infant with severe congenital malformations
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Reference30 articles.
1. Tandem duplication of 11p12-p13 in a child with borderline development delay and eye abnormalities: Dose effect of the PAX6 gene product?
2. Trisomy 10: ultrasound features and natural history after first trimester diagnosis
3. Trisomy 10 mosaicism in a newborn boy; delineation of the syndrome
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4. Identification of paternal uniparental disomy on chromosome 22 and ade novodeletion on chromosome 18 in individuals with orofacial clefts;Molecular Genetics & Genomic Medicine;2018-08-23
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