Inherited 15q24 microdeletion syndrome in twins and their father with phenotypic variability.

Samuelsson, Lena; Zagoras, Theofanis; Hafström, Maria

Samuelsson, Lena; Zagoras, Theofanis; Hafström, Maria.

Afiliação

Samuelsson L; Department of Clinical Genetics, Sahlgrenska University Hospital, Sweden.
Zagoras T; Department of Clinical Genetics, Sahlgrenska University Hospital, Sweden.
Hafström M; Department of Pediatrics, Institute of Clinical Sciences, The Queen Silvia Children's Hospital, University of Gothenburg, Göteborg, Sweden; Department of Paediatrics, St. Olavs Hospital, Norway; Department of Laboratory Medicine, Children's and Women's Health, Norwegian University of Science and Technology, Trondheim, Norway. Electronic address: maria.hafstrom@vgregion.se.

Eur J Med Genet ; 58(2): 111-5, 2015 Feb.

Article em En | MEDLINE | ID: mdl-25527279

Assuntos

Deleção Cromossômica; Transtornos Cromossômicos; Deficiência Intelectual; Gêmeos/genética; Adulto; Cromossomos Humanos Par 15; Pai; Feminino; Humanos; Lactente; Recém-Nascido; Masculino; Fenótipo; Síndrome

Palavras-chave

Chromosome deletion; Chromosome disorders; Chromosomes human pair 15; Intellectual disability; Microarray analysis

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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Gêmeos / Deleção Cromossômica / Transtornos Cromossômicos / Deficiência Intelectual Limite: Adult / Female / Humans / Infant / Male / Newborn Idioma: En Revista: Eur J Med Genet Assunto da revista: GENETICA MEDICA Ano de publicação: 2015 Tipo de documento: Article País de afiliação: Suécia

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