A Xq21.31 duplication without features of Prader–Willi syndrome

Author:

Castro-Gago Manuel,Pérez-Gay Laura,Gómez-Lado Carmen,Barros-Angueira Francisco

Publisher

Springer Science and Business Media LLC

Subject

Endocrinology,Endocrinology, Diabetes and Metabolism

Reference2 articles.

1. P. Pramyothin, M. Pithukpakorn, R.F. Arakaki, A 47, XXY patient and Xq21.31 duplication with features of Prader–Willi syndrome: results of array-based comparative genomic hybridization. Endocrine 37, 379–382 (2010)

2. M.T. Gabbertt, G.B. Peters, J.M. Carmichael, A.P. Darmanian, F.A. Collins, Prader–Willi syndrome phenocopy due to duplication of Xq21.1-q21.31, with array CGH of the critical region. Clin. Genet. 23, 853–859 (2008)

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1. Xq21.1q21.31 Duplication in Two Male Siblings;Molecular Syndromology;2021-11-01

2. De novo Xq21.31–q21.32 duplication in intellectual disability: a new report;Clinical Dysmorphology;2019-04

3. A CNV Catalogue;Human Chromosome Variation: Heteromorphism, Polymorphism and Pathogenesis;2017

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