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Whole exome and targeted sequencing reveal novel mutations associated with inherited PCOS condition in an Indian cohort.
Janani, Dakshina Moorthy; Ramasubramanyan, Sharada; Chellappa, Venkatesh; Santhanam, Rekha; Manickam, Ranjani; Shameli, Jeevamani; Balasundaram, Usha.
Afiliação
  • Janani DM; Department of Genetic Engineering, Faculty of Engineering and Technology, SRM Institute of Science and Technology, SRM Nagar, Kattankulathur, Chennai, 603 203, India.
  • Ramasubramanyan S; Department of Biochemistry and Cell Biology, Vision Research Foundation, Sankara Nethralaya, Chennai, 600 006, India.
  • Chellappa V; Department of Medical Epidemiology and Biostatistics, Karolinska Institute, Solna, 171 77, Stockholm, Sweden.
  • Santhanam R; Department of Genetic Engineering, Faculty of Engineering and Technology, SRM Institute of Science and Technology, SRM Nagar, Kattankulathur, Chennai, 603 203, India.
  • Manickam R; SRM-DBT Platform for Advanced Life Science Technologies, SRM Institute of Science and Technology, Chennai, Tamil Nadu, 603 203, India.
  • Shameli J; Department of Genetic Engineering, Faculty of Engineering and Technology, SRM Institute of Science and Technology, SRM Nagar, Kattankulathur, Chennai, 603 203, India.
  • Balasundaram U; Department of Genetic Engineering, Faculty of Engineering and Technology, SRM Institute of Science and Technology, SRM Nagar, Kattankulathur, Chennai, 603 203, India. sundaram.usha@gmail.com.
J Hum Genet ; 68(1): 39-46, 2023 Jan.
Article em En | MEDLINE | ID: mdl-36284191
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Síndrome do Ovário Policístico Tipo de estudo: Prognostic_studies / Risk_factors_studies Limite: Female / Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article
Texto completo
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Síndrome do Ovário Policístico Tipo de estudo: Prognostic_studies / Risk_factors_studies Limite: Female / Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article