Co-occurrence of a de novo Williams and 22q11.2 microdeletion syndromes.

Shukla, Anju; Mandal, Kausik; Patil, Siddaramappa J; Kishore, Yougal; Phadke, Shubha R; Girisha, Katta M

Shukla, Anju; Mandal, Kausik; Patil, Siddaramappa J; Kishore, Yougal; Phadke, Shubha R; Girisha, Katta M.

Afiliação

Shukla A; Department of Medical Genetics, Kasturba Medical College, Manipal University, Manipal, India.
Mandal K; Department of Medical Genetics, Sanjay Gandhi Postgraduate Institute of Medical Sciences, Lucknow, India.
Patil SJ; Naryana Hrudayalaya Institute of Medical Sciences, Bangalore, Karnataka, India.
Kishore Y; Department of Medical Genetics, Sanjay Gandhi Postgraduate Institute of Medical Sciences, Lucknow, India.
Phadke SR; Department of Medical Genetics, Sanjay Gandhi Postgraduate Institute of Medical Sciences, Lucknow, India.
Girisha KM; Department of Medical Genetics, Kasturba Medical College, Manipal University, Manipal, India.

Am J Med Genet A ; 167A(8): 1927-31, 2015 Aug.

Article em En | MEDLINE | ID: mdl-25898978

Assuntos

Deleção Cromossômica; Cromossomos Humanos Par 22; Síndrome de Williams/genética; Criança; Humanos; Masculino

Palavras-chave

DiGeorge syndrome; Williams syndrome; chromosome 22q11.2 deletion syndrome; chromosome 7q11.23 microdeletion syndrome

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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Cromossomos Humanos Par 22 / Deleção Cromossômica / Síndrome de Williams Limite: Child / Humans / Male Idioma: En Ano de publicação: 2015 Tipo de documento: Article

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