Adult Height, 22q11.2 Deletion Extent, and Short Stature in 22q11.2 Deletion Syndrome.

Heung, Tracy; Conroy, Brigid; Malecki, Sarah; Ha, Joanne; Boot, Erik; Corral, Maria; Bassett, Anne S

Heung, Tracy; Conroy, Brigid; Malecki, Sarah; Ha, Joanne; Boot, Erik; Corral, Maria; Bassett, Anne S.

Afiliação

Heung T; Clinical Genetics Research Program, Centre for Addiction and Mental Health, Toronto, ON M5S 2S1, Canada.
Conroy B; The Dalglish Family 22q Clinic, University Health Network, Toronto, ON M5G 2C4, Canada.
Malecki S; Clinical Genetics Research Program, Centre for Addiction and Mental Health, Toronto, ON M5S 2S1, Canada.
Ha J; Undergraduate Medical Education, Faculty of Medicine, University of Toronto, Toronto, ON M5S 1A4, Canada.
Boot E; Clinical Genetics Research Program, Centre for Addiction and Mental Health, Toronto, ON M5S 2S1, Canada.
Corral M; Department of Medicine, University of Toronto, Toronto, ON M5S 1A4, Canada.
Bassett AS; Clinical Genetics Research Program, Centre for Addiction and Mental Health, Toronto, ON M5S 2S1, Canada.

Genes (Basel) ; 13(11)2022 11 05.

Article em En | MEDLINE | ID: mdl-36360275

Assuntos

Síndrome de DiGeorge; Nanismo; Cardiopatias Congênitas; Deficiência Intelectual; Adulto; Humanos; Criança; Síndrome de DiGeorge/genética; Síndrome de DiGeorge/epidemiologia; Deficiência Intelectual/genética; Cardiopatias Congênitas/genética; Dosagem de Genes

Palavras-chave

DiGeorge syndrome; adult phenotype; copy number variation; quantitative trait; velocardiofacial syndrome

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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Síndrome de DiGeorge / Nanismo / Cardiopatias Congênitas / Deficiência Intelectual Tipo de estudo: Prognostic_studies / Risk_factors_studies Limite: Adult / Child / Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article

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