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Mutational Assessment in NKX2-5 and ACTC1 Genes in Patients with Congenital Cardiac Septal Defect (CCSD) from Ethnic Kashmiri Population.
Nazeer, Nadeem Ul; Bhat, Mohammad Akbar; Rah, Bilal; Bhat, Gh Rasool; Wani, Shadil Ibrahim; Yousuf, Adfar; Dar, Abdul Majeed; Afroze, Dil.
Affiliation
  • Nazeer NU; Department of CVTS, Sheri-Kashmir Institute of Medical Sciences, Srinagar 190011, India.
  • Bhat MA; Department of CVTS, Sheri-Kashmir Institute of Medical Sciences, Srinagar 190011, India.
  • Rah B; Advanced Centre for Human Genetics, Sheri-Kashmir Institute of Medical Sciences, Srinagar 190011, India.
  • Bhat GR; Advanced Centre for Human Genetics, Sheri-Kashmir Institute of Medical Sciences, Srinagar 190011, India.
  • Wani SI; Advanced Centre for Human Genetics, Sheri-Kashmir Institute of Medical Sciences, Srinagar 190011, India.
  • Yousuf A; Advanced Centre for Human Genetics, Sheri-Kashmir Institute of Medical Sciences, Srinagar 190011, India.
  • Dar AM; Department of CVTS, Sheri-Kashmir Institute of Medical Sciences, Srinagar 190011, India.
  • Afroze D; Advanced Centre for Human Genetics, Sheri-Kashmir Institute of Medical Sciences, Srinagar 190011, India.
Int J Environ Res Public Health ; 19(16)2022 08 11.
Article in En | MEDLINE | ID: mdl-36011517
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Heart Septal Defects / Heart Septal Defects, Ventricular Type of study: Prognostic_studies Limits: Humans Language: En Journal: Int J Environ Res Public Health Year: 2022 Document type: Article Affiliation country: Country of publication:
Fulltext
Add to My VHL
Print
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Heart Septal Defects / Heart Septal Defects, Ventricular Type of study: Prognostic_studies Limits: Humans Language: En Journal: Int J Environ Res Public Health Year: 2022 Document type: Article Affiliation country: Country of publication: