Frequency of Sex Chromosome Involvement in a Large Cohort of Subjects with Two Copy Number Variants.

Vara, Autumn; Smith, Janice L; Hashmi, S Shahrukh; Wagner, Victoria F; Gunther, Kathryn; Rodriguez-Buritica, David F

Vara, Autumn; Smith, Janice L; Hashmi, S Shahrukh; Wagner, Victoria F; Gunther, Kathryn; Rodriguez-Buritica, David F.

Afiliação

Vara A; The University of Texas MD Anderson Cancer Center UTHealth Graduate School of Biomedical Sciences, Houston, Texas, USA.
Smith JL; Department of Clinical Cancer Genetics, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
Hashmi SS; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, USA.
Wagner VF; Division of Medical Genetic, Department of Pediatrics, McGovern Medical School at the University of Texas Health Science Center at Houston (UTHealth Houston) and Children's Memorial Hermann Hospital, Houston, Texas, USA.
Gunther K; Division of Medical Genetic, Department of Pediatrics, McGovern Medical School at the University of Texas Health Science Center at Houston (UTHealth Houston) and Children's Memorial Hermann Hospital, Houston, Texas, USA.
Rodriguez-Buritica DF; Clinical Operations, Color Health Inc., Burlingame, California, USA.

Cytogenet Genome Res ; 162(11-12): 599-608, 2022.

Article em En | MEDLINE | ID: mdl-37231787

Palavras-chave

Copy number variants; Dual copy number variant; Sex chromosome

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Prognostic_studies Idioma: En Revista: Cytogenet Genome Res Assunto da revista: GENETICA Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Estados Unidos

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