Literature DB >> 22763470

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

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

Abstract

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Year:  2013        PMID： 22763470     DOI： 10.1007/s12020-012-9738-4

Source DB:  PubMed          Journal:  Endocrine        ISSN： 1355-008X            Impact factor:   3.633


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  2 in total

1.  A 47, XXY patient and Xq21.31 duplication with features of Prader-Willi syndrome: results of array-based comparative genomic hybridization.

Authors:  Pornpoj Pramyothin; Manop Pithukpakorn; Richard F Arakaki
Journal:  Endocrine       Date:  2010-04-09       Impact factor: 3.633

2.  Prader-Willi syndrome phenocopy due to duplication of Xq21.1-q21.31, with array CGH of the critical region.

Authors:  M T Gabbett; G B Peters; J M Carmichael; A P Darmanian; F A Collins
Journal:  Clin Genet       Date:  2008-02-13       Impact factor: 4.438
  2 in total
  1 in total

1.  Xq21.1q21.31 Duplication in Two Male Siblings.

Authors:  Charlotte Ann Sherlaw-Sturrock; Sarah Graham; Anita Morgan; Lisa Reali; Swati Naik
Journal:  Mol Syndromol       Date:  2021-11-01
  1 in total

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