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Microdeletions in 1q21 and 8q12.1 depict two additional molecular subgroups of Silver-Russell syndrome like phenotypes.
Baba, Naomi; Lengyel, Anna; Pinti, Eva; Yapici, Elzem; Schreyer, Isolde; Liehr, Thomas; Fekete, György; Eggermann, Thomas.
Afiliação
  • Baba N; Institute of Human Genetics, University of Jena, Jena, Germany.
  • Lengyel A; Praxis Für Humangenetik, Zentrum Für Ambulante Medizin, Jena, Germany.
  • Pinti E; 2Nd Department of Pediatrics, Semmelweis University Budapest, Budapest, Hungary.
  • Yapici E; 2Nd Department of Pediatrics, Semmelweis University Budapest, Budapest, Hungary.
  • Schreyer I; Institute of Human Genetics, Medical Faculty, RWTH Aachen University, Pauwelsstr. 30, 52074, Aachen, Germany.
  • Liehr T; Institute of Human Genetics, University of Jena, Jena, Germany.
  • Fekete G; Praxis Für Humangenetik, Zentrum Für Ambulante Medizin, Jena, Germany.
  • Eggermann T; Institute of Human Genetics, University of Jena, Jena, Germany.
Mol Cytogenet ; 15(1): 19, 2022 May 13.
Article em En | MEDLINE | ID: mdl-35562807
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2022 Tipo de documento: Article
Texto completo
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2022 Tipo de documento: Article