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Exome sequencing reveals novel variants and unique allelic spectrum for hearing impairment in Filipino cochlear implantees.
Truong, Brittany T; Yarza, Talitha K L; Bootpetch Roberts, Tori; Roberts, Susannah; Xu, Jonathan; Steritz, Matthew J; Tobias-Grasso, Celina A M; Azamian, Mahshid; Lalani, Seema R; Mohlke, Karen L; Lee, Nanette R; Cutiongco-de la Paz, Eva Maria; Reyes-Quintos, Maria Rina T; Santos-Cortez, Regie Lyn P; Chiong, Charlotte M.
Afiliação
  • Truong BT; Human Medical Genetics and Genomics Program, University of Colorado School of Medicine, Aurora, Colorado.
  • Yarza TKL; Philippine National Ear Institute, University of the Philippines (UP) Manila-National Institutes of Health (NIH), Manila, Philippines.
  • Bootpetch Roberts T; Newborn Hearing Screening Reference Center, UP Manila-NIH, Manila, Philippines.
  • Roberts S; Department of Otolaryngology, University of Colorado School of Medicine, Aurora, Colorado.
  • Xu J; Department of Otolaryngology, University of Colorado School of Medicine, Aurora, Colorado.
  • Steritz MJ; Department of Otolaryngology, University of Colorado School of Medicine, Aurora, Colorado.
  • Tobias-Grasso CAM; Department of Otolaryngology, University of Colorado School of Medicine, Aurora, Colorado.
  • Azamian M; MED-EL, Innsbruck, Austria.
  • Lalani SR; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas.
  • Mohlke KL; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas.
  • Lee NR; Department of Genetics, University of North Carolina, Chapel Hill, North Carolina.
  • Cutiongco-de la Paz EM; Office of Population Studies Foundation and Department of Anthropology, Sociology and History, University of San Carlos, Cebu, Philippines.
  • Reyes-Quintos MRT; UP Manila-NIH, Manila 1000, Philippines.
  • Santos-Cortez RLP; Philippine Genome Center, Quezon City, Philippines.
  • Chiong CM; Philippine National Ear Institute, University of the Philippines (UP) Manila-National Institutes of Health (NIH), Manila, Philippines.
Clin Genet ; 95(5): 634-636, 2019 05.
Article em En | MEDLINE | ID: mdl-30828794
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Alelos / Sequenciamento do Exoma / Perda Auditiva / Mutação Limite: Adult / Child / Humans País/Região como assunto: Asia Idioma: En Ano de publicação: 2019 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Alelos / Sequenciamento do Exoma / Perda Auditiva / Mutação Limite: Adult / Child / Humans País/Região como assunto: Asia Idioma: En Ano de publicação: 2019 Tipo de documento: Article