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Costello syndrome: Clinical phenotype, genotype, and management guidelines.
Gripp, Karen W; Morse, Lindsey A; Axelrad, Marni; Chatfield, Kathryn C; Chidekel, Aaron; Dobyns, William; Doyle, Daniel; Kerr, Bronwyn; Lin, Angela E; Schwartz, David D; Sibbles, Barbara J; Siegel, Dawn; Shankar, Suma P; Stevenson, David A; Thacker, Mihir M; Weaver, K Nicole; White, Sue M; Rauen, Katherine A.
Afiliación
  • Gripp KW; Division of Medical Genetics, Department of Pediatrics, A.I. duPont Hospital for Children, Wilmington, Delaware.
  • Morse LA; Ferre Institute, Binghamton, New York, New York.
  • Axelrad M; Psychology Section, Department of Pediatrics, Baylor College of Medicine, Houston, Texas.
  • Chatfield KC; Section of Cardiology, Department of Pediatrics, University of Colorado School of Medicine, Aurora, Colorado.
  • Chidekel A; Division of Pulmonology, Department of Pediatrics, A.I. duPont Hospital for Children, Wilmington, Delaware.
  • Dobyns W; Division of Medical Genetics, Seattle Children's Hospital, Seattle, Washington.
  • Doyle D; Division of Endocrinology, A.I. duPont Hospital for Children, Wilmington, Delaware.
  • Kerr B; Manchester Center for Genomic Medicine, University of Manchester, Manchester, UK.
  • Lin AE; Medical Genetics Unit, Department of Pediatrics, MassGeneral Hospital for Children, Boston, Massachusetts.
  • Schwartz DD; Psychology Section, Department of Pediatrics, Baylor College of Medicine, Houston, Texas.
  • Sibbles BJ; Division of Pediatrics, Erasmus MC-Sophia Children's Hospital, Rotterdam, the Netherlands.
  • Siegel D; Department of Dermatology, Medical College of Wisconsin, Milwaukee, Wisconsin.
  • Shankar SP; Division of Genomic Medicine, Department of Pediatrics, University of California Davis, Sacramento, California.
  • Stevenson DA; Division of Medical Genetic, Department of Pediatrics, Stanford University, Palo Alto, California.
  • Thacker MM; Department of Orthopedic Surgery, Nemoirs-Alfred I. duPont Hospital for Children, Wilmington, Delaware.
  • Weaver KN; Division of Human Genetics, University of Cincinnati College of Medicine, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio.
  • White SM; Victorian Clinical Genetics Services, Royal Children's Hospital, Victoria, Australia.
  • Rauen KA; Division of Genomic Medicine, Department of Pediatrics, University of California Davis, Sacramento, California.
Am J Med Genet A ; 179(9): 1725-1744, 2019 09.
Article en En | MEDLINE | ID: mdl-31222966
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Anomalías Múltiples / Proteínas Proto-Oncogénicas p21(ras) / Síndrome de Costello / Corazón Tipo de estudio: Guideline Límite: Humans Idioma: En Año: 2019 Tipo del documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Anomalías Múltiples / Proteínas Proto-Oncogénicas p21(ras) / Síndrome de Costello / Corazón Tipo de estudio: Guideline Límite: Humans Idioma: En Año: 2019 Tipo del documento: Article