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Developmental genomics of limb malformations: Allelic series in association with gene dosage effects contribute to the clinical variability.
Duan, Ruizhi; Hijazi, Hadia; Gulec, Elif Yilmaz; Eker, Hatice Koçak; Costa, Silvia R; Sahin, Yavuz; Ocak, Zeynep; Isikay, Sedat; Ozalp, Ozge; Bozdogan, Sevcan; Aslan, Huseyin; Elcioglu, Nursel; Bertola, Débora R; Gezdirici, Alper; Du, Haowei; Fatih, Jawid M; Grochowski, Christopher M; Akay, Gulsen; Jhangiani, Shalini N; Karaca, Ender; Gu, Shen; Coban-Akdemir, Zeynep; Posey, Jennifer E; Bayram, Yavuz; Sutton, V Reid; Carvalho, Claudia M B; Pehlivan, Davut; Gibbs, Richard A; Lupski, James R.
Afiliación
  • Duan R; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA.
  • Hijazi H; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA.
  • Gulec EY; Department of Medical Genetics, School of Medicine, Istanbul Medeniyet University, Istanbul, Turkey.
  • Eker HK; Department of Medical Genetics, Konya City Hospital, Konya, Turkey.
  • Costa SR; Human Genome and Stem Cell Research Center, Institute of Bioscience, Universidade de São Paulo, São Paulo, Brazil.
  • Sahin Y; Medical Genetics, Genoks Genetics Center, Ankara, Turkey.
  • Ocak Z; Department of Medical Genetics, Faculty of Medicine, Istinye University, Istanbul, Turkey.
  • Isikay S; Department of Pediatric Neurology, Faculty of Medicine, Gaziantep University, Gaziantep, Turkey.
  • Ozalp O; Department of Medical Genetics, Adana City Training and Research Hospital, Adana, Turkey.
  • Bozdogan S; Department of Medical Genetics, Faculty of Medicine, Cukurova University, Adana, Turkey.
  • Aslan H; Department of Medical Genetics, Adana City Training and Research Hospital, Adana, Turkey.
  • Elcioglu N; Department of Pediatric Genetics, School of Medicine, Marmara University, Istanbul, Turkey.
  • Bertola DR; Eastern Mediterranean University Medical School, Magosa, 10 Mersin, Turkey.
  • Gezdirici A; Human Genome and Stem Cell Research Center, Institute of Bioscience, Universidade de São Paulo, São Paulo, Brazil.
  • Du H; Genetics Unit, Instituto da Criança do Hospital das Clínicas da Faculdade de Medicina, Universidade de São Paulo, São Paulo, Brazil.
  • Fatih JM; Department of Medical Genetics, Basaksehir Cam and Sakura City Hospital, Istanbul, Turkey.
  • Grochowski CM; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA.
  • Akay G; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA.
  • Jhangiani SN; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA.
  • Gu S; Human Genome Sequencing Center, Baylor College of Medicine, Houston, TX, USA.
  • Coban-Akdemir Z; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA.
  • Posey JE; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA.
  • Bayram Y; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA.
  • Sutton VR; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA.
  • Carvalho CMB; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA.
  • Pehlivan D; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA.
  • Gibbs RA; Texas Children's Hospital, Houston, TX, USA.
  • Lupski JR; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA.
HGG Adv ; 3(4): 100132, 2022 Oct 13.
Article en En | MEDLINE | ID: mdl-36035248
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Prognostic_studies / Risk_factors_studies Idioma: En Revista: HGG Adv Año: 2022 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Estados Unidos
Texto completo
Añadir a Mi BVS
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Prognostic_studies / Risk_factors_studies Idioma: En Revista: HGG Adv Año: 2022 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Estados Unidos