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Implications of VEGF gene sequence variations and its expression in recurrent pregnancy loss.
Amin, Ina; Pandith, Arshad A; Manzoor, Usma; Mir, Syed Hussain; Afroze, Dil; Koul, Aabid Mustafa; Wani, Saima; Ahmad, Aabida; Qasim, Iqbal; Rashid, Masarat; Wani, Umer M; Anwar, Iqra; Aein, Qurat Ul; Mansoor, Sheikh.
Afiliação
  • Amin I; Advanced Centre for Human Genetics, Sher-I-Kashmir Institute of Medical Sciences (SKIMS), J&K-India; Department of Clinical Biochemistry, University of Kashmir Jammu and Kashmir, India.
  • Pandith AA; Advanced Centre for Human Genetics, Sher-I-Kashmir Institute of Medical Sciences (SKIMS), J&K-India. Electronic address: arshaajiz@gmail.com.
  • Manzoor U; Advanced Centre for Human Genetics, Sher-I-Kashmir Institute of Medical Sciences (SKIMS), J&K-India.
  • Mir SH; Department of Clinical Biochemistry, University of Kashmir Jammu and Kashmir, India.
  • Afroze D; Advanced Centre for Human Genetics, Sher-I-Kashmir Institute of Medical Sciences (SKIMS), J&K-India. Electronic address: afrozedil@gmail.com.
  • Koul AM; Advanced Centre for Human Genetics, Sher-I-Kashmir Institute of Medical Sciences (SKIMS), J&K-India.
  • Wani S; Department of Obstetrics and Gynecology SKIMS, Srinagar Jammu and Kashmir, India.
  • Ahmad A; Department of Obstetrics and Gynecology SKIMS, Srinagar Jammu and Kashmir, India.
  • Qasim I; Advanced Centre for Human Genetics, Sher-I-Kashmir Institute of Medical Sciences (SKIMS), J&K-India.
  • Rashid M; Department of Obstetrics and Gynecology SKIMS, Srinagar Jammu and Kashmir, India.
  • Wani UM; Department of Biotechnology, University of Kashmir Jammu and Kashmir, India.
  • Anwar I; Advanced Centre for Human Genetics, Sher-I-Kashmir Institute of Medical Sciences (SKIMS), J&K-India.
  • Aein QU; Advanced Centre for Human Genetics, Sher-I-Kashmir Institute of Medical Sciences (SKIMS), J&K-India.
  • Mansoor S; Advanced Centre for Human Genetics, Sher-I-Kashmir Institute of Medical Sciences (SKIMS), J&K-India.
Reprod Biomed Online ; 43(6): 1035-1044, 2021 12.
Article em En | MEDLINE | ID: mdl-34716101
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Aborto Habitual / Predisposição Genética para Doença / Polimorfismo de Nucleotídeo Único / Fator A de Crescimento do Endotélio Vascular / Alelos Tipo de estudo: Observational_studies / Risk_factors_studies Limite: Adult / Female / Humans / Pregnancy Idioma: En Revista: Reprod Biomed Online Assunto da revista: MEDICINA REPRODUTIVA Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Índia
Texto completo
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Aborto Habitual / Predisposição Genética para Doença / Polimorfismo de Nucleotídeo Único / Fator A de Crescimento do Endotélio Vascular / Alelos Tipo de estudo: Observational_studies / Risk_factors_studies Limite: Adult / Female / Humans / Pregnancy Idioma: En Revista: Reprod Biomed Online Assunto da revista: MEDICINA REPRODUTIVA Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Índia