Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Vaghasia Kk"'
Publikováno v:
The Application of Clinical Genetics, Vol Volume 10, Pp 27-35 (2017)
Parth S Shah,1 Nidhi D Shah,2 Hari Shankar P Ray,3 Nikunj B Khatri,3 Ketan K Vaghasia,3 Rutvik J Raval,4 Sandip C Shah,3 Mandava V Rao5 1Department of Medicine, Lahey Hospital and Medical Center, Boston, MA, 2Department of Pediatrics, Nassau Universi
Externí odkaz:
https://doaj.org/article/c008a60cab4e4fadb4139e8a50eea319
Publikováno v:
Journal of Clinical and Diagnostic Research, Vol 11, Iss 9, Pp GD01-GD03 (2017)
The mutations in Haemoglobin Beta (HBB) gene, bring about less or no production of Hb β-chain synthesis in affected cases, leading from minor to major types depending on haematological indices. In compound heterozygotic conditions, two traits are in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::892e2fe1dabe27bf060cd10e15686a77
Autor:
Shah PS; Chief Scientific Officer (CSO), Molecular Genomics, Supratech Micropath Laboratory and Research Institute, Ahmedabad, Gujarat, India., Ray HSP; Research Scientist, Supratech Micropath Laboratory and Research Institute, Ahmedabad, Gujarat, India., Vaghasia KK; Senior Scientist, Supratech Micropath Laboratory and Research Institute, Ahmedabad, Gujarat, India., Shah SC; Laboratory Director, Supratech Micropath Laboratory and Research Institute, Ahmedabad, Gujarat, India., Rao MV; Ex. Director, School of Sciences, Gujarat University, Ahmedabad, Gujarat, India.
Publikováno v:
Journal of clinical and diagnostic research : JCDR [J Clin Diagn Res] 2017 Sep; Vol. 11 (9), pp. GD01-GD03. Date of Electronic Publication: 2017 Sep 01.