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CMA analysis identifies homozygous deletion of MCPH1 in 2 brothers with primary Microcephaly-1.
Hemmat, Morteza; Rumple, Melissa J; Mahon, Loretta W; Morrow, Melanie; Zach, Tamara; Anguiano, Arturo; Elnaggar, Mohamed M; Wang, Boris T; Boyar, Fatih Z.
Afiliación
  • Hemmat M; Quest Diagnostics Nichols Institute, 33608 Ortega Highway, San Juan Capistrano, CA USA.
  • Rumple MJ; Banner Child Neurology, 5310 W Thunderbird Rd, Ste 301, Glendale, AZ 85306 USA.
  • Mahon LW; Quest Diagnostics Nichols Institute, 33608 Ortega Highway, San Juan Capistrano, CA USA.
  • Morrow M; Banner Child Neurology, 5310 W Thunderbird Rd, Ste 301, Glendale, AZ 85306 USA.
  • Zach T; Banner Child Neurology, 5310 W Thunderbird Rd, Ste 301, Glendale, AZ 85306 USA.
  • Anguiano A; Quest Diagnostics Nichols Institute, 33608 Ortega Highway, San Juan Capistrano, CA USA.
  • Elnaggar MM; Quest Diagnostics Nichols Institute, 33608 Ortega Highway, San Juan Capistrano, CA USA.
  • Wang BT; Quest Diagnostics Nichols Institute, 33608 Ortega Highway, San Juan Capistrano, CA USA.
  • Boyar FZ; Quest Diagnostics Nichols Institute, 33608 Ortega Highway, San Juan Capistrano, CA USA.
Mol Cytogenet ; 10: 33, 2017.
Article en En | MEDLINE | ID: mdl-28878824
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Texto completo: 1 Banco de datos: MEDLINE Tipo de estudio: Observational_studies / Prognostic_studies / Risk_factors_studies Idioma: En Revista: Mol Cytogenet Año: 2017 Tipo del documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Banco de datos: MEDLINE Tipo de estudio: Observational_studies / Prognostic_studies / Risk_factors_studies Idioma: En Revista: Mol Cytogenet Año: 2017 Tipo del documento: Article