The first antenatal diagnosis of KBG syndrome: a microdeletion at chromosome 16q24.2q24.3 containing multiple genes including ANKRD11 associated with the disorder.

Hodgetts Morton, Victoria; Quinlan-Jones, Elizabeth; Butts, Natasha; Williams, Denise; Hamilton, Sue; Marton, Tamas; Morris, Katie

Hodgetts Morton, Victoria; Quinlan-Jones, Elizabeth; Butts, Natasha; Williams, Denise; Hamilton, Sue; Marton, Tamas; Morris, Katie.

Afiliação

Hodgetts Morton V; Birmingham Women's Hospital Mindelsohn Way Birmingham B15 2TG UK.
Quinlan-Jones E; Institute of Metabolism and Systems Research University of Birmingham Birmingham B15 2 TT UK.
Butts N; Birmingham Women's Hospital Mindelsohn Way Birmingham B15 2TG UK.
Williams D; Birmingham Women's Hospital Mindelsohn Way Birmingham B15 2TG UK.
Hamilton S; Birmingham Women's Hospital Mindelsohn Way Birmingham B15 2TG UK.
Marton T; Birmingham Women's Hospital Mindelsohn Way Birmingham B15 2TG UK.
Morris K; Birmingham Women's Hospital Mindelsohn Way Birmingham B15 2TG UK.

Clin Case Rep ; 6(1): 189-191, 2018 01.

Article em En | MEDLINE | ID: mdl-29375862

Palavras-chave

ANKRD11; KBG syndrome; prenatal diagnosis

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Diagnostic_studies / Risk_factors_studies Idioma: En Ano de publicação: 2018 Tipo de documento: Article

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