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Renpenning syndrome in a female.
Cho, Raymond Y; Peñaherrera, Maria S; Du Souich, Christele; Huang, Lijia; Mwenifumbo, Jill; Nelson, Tanya N; Elliott, Alison M; Adam, Shelin; Eydoux, Patrice; Yang, Gui X; Chijiwa, Chieko; Van Allen, Margot I; Friedman, Jan M; Robinson, Wendy P; Lehman, Anna.
Afiliación
  • Cho RY; Department of Medical Genetics, University of British Columbia, Vancouver, British Columbia, Canada.
  • Peñaherrera MS; Department of Medical Genetics, University of British Columbia, Vancouver, British Columbia, Canada.
  • Du Souich C; BC Children's Hospital Research Institute, Vancouver, British Columbia, Canada.
  • Huang L; Department of Medical Genetics, University of British Columbia, Vancouver, British Columbia, Canada.
  • Mwenifumbo J; BC Children's Hospital Research Institute, Vancouver, British Columbia, Canada.
  • Nelson TN; Department of Pathology and Laboratory Medicine, University of British Columbia, Vancouver, British Columbia, Canada.
  • Elliott AM; Department of Medical Genetics, University of British Columbia, Vancouver, British Columbia, Canada.
  • Adam S; Department of Medical Genetics, University of British Columbia, Vancouver, British Columbia, Canada.
  • Eydoux P; BC Children's Hospital Research Institute, Vancouver, British Columbia, Canada.
  • Yang GX; Department of Medical Genetics, University of British Columbia, Vancouver, British Columbia, Canada.
  • Chijiwa C; Department of Medical Genetics, University of British Columbia, Vancouver, British Columbia, Canada.
  • Van Allen MI; Department of Medical Genetics, University of British Columbia, Vancouver, British Columbia, Canada.
  • Friedman JM; Department of Medical Genetics, University of British Columbia, Vancouver, British Columbia, Canada.
  • Robinson WP; Department of Pathology and Laboratory Medicine, University of British Columbia, Vancouver, British Columbia, Canada.
  • Lehman A; BC Children's Hospital Research Institute, Vancouver, British Columbia, Canada.
Am J Med Genet A ; 182(3): 498-503, 2020 03.
Article en En | MEDLINE | ID: mdl-31840929
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Anomalías Múltiples / Parálisis Cerebral / Discapacidad Intelectual Ligada al Cromosoma X / Enfermedades Genéticas Ligadas al Cromosoma X / Proteínas de Unión al ADN Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Child / Female / Humans / Male Idioma: En Revista: Am J Med Genet A Asunto de la revista: GENETICA MEDICA Año: 2020 Tipo del documento: Article País de afiliación: Canadá
Texto completo
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Anomalías Múltiples / Parálisis Cerebral / Discapacidad Intelectual Ligada al Cromosoma X / Enfermedades Genéticas Ligadas al Cromosoma X / Proteínas de Unión al ADN Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Child / Female / Humans / Male Idioma: En Revista: Am J Med Genet A Asunto de la revista: GENETICA MEDICA Año: 2020 Tipo del documento: Article País de afiliación: Canadá