IGF1R mutation analysis in short children with Silver-Russell syndrome features.

Soellner, Lukas; Spengler, Sabrina; Begemann, Matthias; Wollmann, Hartmut A; Binder, Gerhard; Eggermann, Thomas

Soellner, Lukas; Spengler, Sabrina; Begemann, Matthias; Wollmann, Hartmut A; Binder, Gerhard; Eggermann, Thomas.

Afiliación

Soellner L; Institute of Human Genetics, University Hospital, Technical University Aachen, Germany.
Spengler S; Institute of Human Genetics, University Hospital, Technical University Aachen, Germany.
Begemann M; Institute of Human Genetics, University Hospital, Technical University Aachen, Germany.
Wollmann HA; Pfizer Ltd, Tadworth, UK.
Binder G; Children's Hospital, University of Tuebingen, Germany.
Eggermann T; Institute of Human Genetics, University Hospital, Technical University Aachen, Germany.

J Pediatr Genet ; 2(3): 113-7, 2013 Sep.

Article en En | MEDLINE | ID: mdl-27625849

Palabras clave

IGF1R mutations; Silver-Russell syndrome; growth retardation

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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Prognostic_studies Idioma: En Revista: J Pediatr Genet Año: 2013 Tipo del documento: Article País de afiliación: Alemania Pais de publicación: Alemania

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