Anomalies of the genitourinary tract in children with 22q11.2 deletion syndrome.

Van Batavia, Jason P; Crowley, Terrence B; Burrows, Evanette; Zackai, Elaine H; Sanna-Cherchi, Simone; McDonald-McGinn, Donna M; Kolon, Thomas F

Van Batavia, Jason P; Crowley, Terrence B; Burrows, Evanette; Zackai, Elaine H; Sanna-Cherchi, Simone; McDonald-McGinn, Donna M; Kolon, Thomas F.

Afiliação

Van Batavia JP; Division of Urology, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.
Crowley TB; Division of Human Genetics, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.
Burrows E; Division of Human Genetics, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.
Zackai EH; Division of Human Genetics, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.
Sanna-Cherchi S; Division of Nephrology, New York-Presbyterian Hospital Columbia University Medical Center, New York, New York.
McDonald-McGinn DM; Division of Human Genetics, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.
Kolon TF; Division of Urology, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.

Am J Med Genet A ; 179(3): 381-385, 2019 03.

Article em En | MEDLINE | ID: mdl-30582277

Assuntos

Síndrome de DiGeorge/diagnóstico; Estudos de Associação Genética; Fenótipo; Anormalidades Urogenitais/diagnóstico; Criança; Pré-Escolar; Síndrome de DiGeorge/epidemiologia; Feminino; Loci Gênicos; Humanos; Lactente; Masculino; Prevalência; Estudos Retrospectivos

Palavras-chave

22q11.2 deletion syndrome; DiGeorge syndrome; genitourinary; pediatrics; renal; urology

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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Fenótipo / Anormalidades Urogenitais / Síndrome de DiGeorge / Estudos de Associação Genética Tipo de estudo: Observational_studies / Prevalence_studies / Prognostic_studies / Risk_factors_studies Limite: Child / Child, preschool / Female / Humans / Infant / Male Idioma: En Ano de publicação: 2019 Tipo de documento: Article

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