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High-Throughput Methylation-Specific Triplet-Primed PCR and Melting Curve Analysis for Selective and Reliable Identification of Actionable FMR1 Genotypes.
Rajan-Babu, Indhu-Shree; Phang, Gui-Ping; Law, Hai-Yang; Lee, Caroline G; Chong, Samuel S.
Afiliação
  • Rajan-Babu IS; Department of Pediatrics, Yong Loo Lin School of Medicine, National University of Singapore, Singapore; Department of Medical Genetics, University of British Columbia, and Children's and Women's Hospital, Vancouver, British Columbia, Canada. Electronic address: indhu.babu@bcchr.ca.
  • Phang GP; Department of Pediatrics, Yong Loo Lin School of Medicine, National University of Singapore, Singapore.
  • Law HY; Department of Pediatric Medicine, KK Women's and Children's Hospital, Singapore.
  • Lee CG; Department of Biochemistry, Yong Loo Lin School of Medicine, National University of Singapore, Singapore; Division of Cellular and Molecular Research, Humphrey Oei Institute of Cancer Research, National Cancer Centre Singapore, Singapore; Cancer and Stem Cell Biology Program, Duke-NUS Medical School
  • Chong SS; Department of Pediatrics, Yong Loo Lin School of Medicine, National University of Singapore, Singapore; Department of Obstetrics and Gynecology, Yong Loo Lin School of Medicine, National University of Singapore, Singapore; Department of Laboratory Medicine, National University Hospital, Singapore. E
J Mol Diagn ; 24(3): 241-252, 2022 03.
Article em En | MEDLINE | ID: mdl-35038595
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Proteína do X Frágil da Deficiência Intelectual / Síndrome do Cromossomo X Frágil Tipo de estudo: Diagnostic_studies / Prognostic_studies Limite: Female / Humans / Male / Newborn Idioma: En Revista: J Mol Diagn Assunto da revista: BIOLOGIA MOLECULAR Ano de publicação: 2022 Tipo de documento: Article
Texto completo
Adicionar na Minha BVS
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XML
PubMed Links
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Proteína do X Frágil da Deficiência Intelectual / Síndrome do Cromossomo X Frágil Tipo de estudo: Diagnostic_studies / Prognostic_studies Limite: Female / Humans / Male / Newborn Idioma: En Revista: J Mol Diagn Assunto da revista: BIOLOGIA MOLECULAR Ano de publicação: 2022 Tipo de documento: Article