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Advancing RAS/RASopathy therapies: An NCI-sponsored intramural and extramural collaboration for the study of RASopathies.
Gross, Andrea M; Frone, Megan; Gripp, Karen W; Gelb, Bruce D; Schoyer, Lisa; Schill, Lisa; Stronach, Beth; Biesecker, Leslie G; Esposito, Dominic; Hernandez, Edjay Ralph; Legius, Eric; Loh, Mignon L; Martin, Staci; Morrison, Deborah K; Rauen, Katherine A; Wolters, Pamela L; Zand, Dina; McCormick, Frank; Savage, Sharon A; Stewart, Douglas R; Widemann, Brigitte C; Yohe, Marielle E.
Afiliación
  • Gross AM; Pediatric Oncology Branch, Center for Cancer Research, National Cancer Institute, Bethesda, Maryland.
  • Frone M; Clinical Genetics Branch, Division of Cancer Epidemiology and Genetics, National Cancer Institute, Rockville, Maryland.
  • Gripp KW; Department of Genetics, Division of Pediatrics, Al duPont Hospital for Children, Wilmington, Delaware.
  • Gelb BD; Department of Pediatrics, Mindich Child Health and Development Institute, Icahn School of Medicine at Mount Sinai, New York, New York.
  • Schoyer L; Department of Genetics and Genomic Sciences, Mindich Child Health and Development Institute, Icahn School of Medicine at Mount Sinai, New York, New York.
  • Schill L; RASopathies Network, Altadena, California.
  • Stronach B; RASopathies Network, Altadena, California.
  • Biesecker LG; RASopathies Network, Altadena, California.
  • Esposito D; Medical Genomics and Metabolic Genetics Branch, National Human Genome Research Institute, Bethesda, Maryland.
  • Hernandez ER; NCI RAS Initiative, Frederick National Laboratory for Cancer Research, Frederick, Maryland.
  • Legius E; Pediatric Oncology Branch, Center for Cancer Research, National Cancer Institute, Bethesda, Maryland.
  • Loh ML; Laboratory for Neurofibromatosis Research, Department of Human Genetics, KU Leuven University Hospital, Leuven, Belgium.
  • Martin S; Department of Pediatrics, Benioff Children's Hospital and the Helen Diller Family Comprehensive Cancer Center, University of California San Francisco, San Francisco, California.
  • Morrison DK; Pediatric Oncology Branch, Center for Cancer Research, National Cancer Institute, Bethesda, Maryland.
  • Rauen KA; Laboratory of Cell and Developmental Signaling, Center for Cancer Research, National Cancer Institute, Frederick, Maryland.
  • Wolters PL; Department of Pediatrics, Division of Genomic Medicine, University of California Davis, Sacramento, California.
  • Zand D; Pediatric Oncology Branch, Center for Cancer Research, National Cancer Institute, Bethesda, Maryland.
  • McCormick F; Center for Drug Evaluation and Research, Food and Drug Administration, Rockville, Maryland.
  • Savage SA; NCI RAS Initiative, Frederick National Laboratory for Cancer Research, Frederick, Maryland.
  • Stewart DR; Clinical Genetics Branch, Division of Cancer Epidemiology and Genetics, National Cancer Institute, Rockville, Maryland.
  • Widemann BC; Clinical Genetics Branch, Division of Cancer Epidemiology and Genetics, National Cancer Institute, Rockville, Maryland.
  • Yohe ME; Pediatric Oncology Branch, Center for Cancer Research, National Cancer Institute, Bethesda, Maryland.
Am J Med Genet A ; 182(4): 866-876, 2020 04.
Article en En | MEDLINE | ID: mdl-31913576
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Displasia Ectodérmica / Neurofibromatosis 1 / Proteínas ras / Insuficiencia de Crecimiento / Síndrome de Costello / Terapia Molecular Dirigida / Cardiopatías Congénitas / Mutación / Síndrome de Noonan Tipo de estudio: Observational_studies / Risk_factors_studies Límite: Humans País/Región como asunto: America do norte Idioma: En Revista: Am J Med Genet A Asunto de la revista: GENETICA MEDICA Año: 2020 Tipo del documento: Article Pais de publicación: Estados Unidos
Texto completo
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Displasia Ectodérmica / Neurofibromatosis 1 / Proteínas ras / Insuficiencia de Crecimiento / Síndrome de Costello / Terapia Molecular Dirigida / Cardiopatías Congénitas / Mutación / Síndrome de Noonan Tipo de estudio: Observational_studies / Risk_factors_studies Límite: Humans País/Región como asunto: America do norte Idioma: En Revista: Am J Med Genet A Asunto de la revista: GENETICA MEDICA Año: 2020 Tipo del documento: Article Pais de publicación: Estados Unidos