Deletion of 16q22.2q23.3 in a Boy with a Phenotype Reminiscent of Silver-Russell Syndrome.

Lengyel, Anna; Pinti, Éva; Eggermann, Thomas; Fekete, György; Haltrich, Irén

Lengyel, Anna; Pinti, Éva; Eggermann, Thomas; Fekete, György; Haltrich, Irén.

Afiliação

Lengyel A; 2nd Department of Pediatrics, Semmelweis University, Budapest, Hungary.
Pinti É; 2nd Department of Pediatrics, Semmelweis University, Budapest, Hungary.
Eggermann T; Institute of Human Genetics, Medical Faculty, RWTH Aachen University, Aachen, Germany.
Fekete G; 2nd Department of Pediatrics, Semmelweis University, Budapest, Hungary.
Haltrich I; 2nd Department of Pediatrics, Semmelweis University, Budapest, Hungary.

Mol Syndromol ; 12(5): 300-304, 2021 Aug.

Article em En | MEDLINE | ID: mdl-34602957

Palavras-chave

Chromosome 16q; Copy number variation; Deletion; Growth delay; Neurodevelopmental disorders

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Mol Syndromol Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Hungria País de publicação: Suíça

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