An Atypical 15q11.2 Microdeletion Not Involving <i>SNORD116</i> Resulting in Prader-Willi Syndrome.

Crenshaw, Molly M; Graw, Sharon L; Slavov, Dobromir; Boyle, Theresa A; Piqué, Daniel G; Taylor, Matthew; Baker, Peter

An Atypical 15q11.2 Microdeletion Not Involving SNORD116 Resulting in Prader-Willi Syndrome.

Crenshaw, Molly M; Graw, Sharon L; Slavov, Dobromir; Boyle, Theresa A; Piqué, Daniel G; Taylor, Matthew; Baker, Peter.

Afiliação

Crenshaw MM; University of Colorado School of Medicine (CU-SOM), Department of Pediatrics, Section of Genetics and Metabolism, Aurora, Colorado, USA.
Graw SL; Colorado Genetics Laboratory, Department of Pathology, University of Colorado Anschutz Medical Campus, Aurora, Colorado, USA.
Slavov D; Division of Cardiology, Cardiovascular Institute, University of Colorado Anschutz Medical Campus, Aurora, Colorado, USA.
Boyle TA; Department of Pathology, Stanford University, Palo Alto, California, USA.
Piqué DG; University of Colorado School of Medicine (CU-SOM), Department of Pediatrics, Section of Genetics and Metabolism, Aurora, Colorado, USA.
Taylor M; Adult Medical Genetics Program, Department of Medicine, University of Colorado Anschutz Medical Campus, Aurora, Colorado, USA.
Baker P; University of Colorado School of Medicine (CU-SOM), Department of Pediatrics, Section of Genetics and Metabolism, Aurora, Colorado, USA.

Case Rep Genet ; 2023: 4225092, 2023.

Article em En | MEDLINE | ID: mdl-37736297

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2023 Tipo de documento: Article

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2023 Tipo de documento: Article