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Second patient with GNB2-related neurodevelopmental disease: Further evidence for a gene-disease association.
Lansdon, Lisa A; Fleming, Emily A; Viso, Florencia Del; Sullivan, Bonnie R; Saunders, Carol J.
Afiliación
  • Lansdon LA; Department of Pathology and Laboratory Medicine, Children's Mercy-Kansas City, 2401 Gillham Road, Kansas City, MO, USA; Genomic Medicine Center, Children's Mercy-Kansas City, 2401 Gillham Road, Kansas City, MO, USA.
  • Fleming EA; Division of Clinical Genetics, Children's Mercy-Kansas City, 2401 Gillham Road, Kansas City, MO, USA.
  • Viso FD; Department of Pathology and Laboratory Medicine, Children's Mercy-Kansas City, 2401 Gillham Road, Kansas City, MO, USA; Genomic Medicine Center, Children's Mercy-Kansas City, 2401 Gillham Road, Kansas City, MO, USA.
  • Sullivan BR; Division of Clinical Genetics, Children's Mercy-Kansas City, 2401 Gillham Road, Kansas City, MO, USA; University of Missouri-Kansas City, School of Medicine, 2411 Holmes Street, Kansas City, MO, USA.
  • Saunders CJ; Department of Pathology and Laboratory Medicine, Children's Mercy-Kansas City, 2401 Gillham Road, Kansas City, MO, USA; Genomic Medicine Center, Children's Mercy-Kansas City, 2401 Gillham Road, Kansas City, MO, USA; University of Missouri-Kansas City, School of Medicine, 2411 Holmes Street, Kansas C
Eur J Med Genet ; 64(7): 104243, 2021 Jul.
Article en En | MEDLINE | ID: mdl-33971351
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Fenotipo / Discapacidades del Desarrollo / Anomalías Craneofaciales / Proteínas de Unión al GTP / Epilepsia Tipo de estudio: Risk_factors_studies Límite: Adolescent / Female / Humans Idioma: En Revista: Eur J Med Genet Asunto de la revista: GENETICA MEDICA Año: 2021 Tipo del documento: Article País de afiliación: Estados Unidos
Texto completo
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Fenotipo / Discapacidades del Desarrollo / Anomalías Craneofaciales / Proteínas de Unión al GTP / Epilepsia Tipo de estudio: Risk_factors_studies Límite: Adolescent / Female / Humans Idioma: En Revista: Eur J Med Genet Asunto de la revista: GENETICA MEDICA Año: 2021 Tipo del documento: Article País de afiliación: Estados Unidos