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Kunal Ray

Showing results (21-30 of 113) with videos related to

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Human Genetics|June 29, 2007
Gene symbol: CYP1B1Kunal Ray, Moulinath Acharya, Suddhasil Mookherjee
Human Genetics|June 29, 2007
Gene symbol: CYP1B1Kunal Ray, Moulinath Acharya, Suddhasil Mookherjee
Human Genetics|June 29, 2007
Gene symbol: SLC45A2Kunal Ray, Moumita Chaki, Mainak Sengupta
Human Genetics|April 3, 2008
Novel human pathological mutations. Gene symbol: TYR. Disease: tyrosinase deficiencyKunal Ray, Moumita Chaki, Mainak Sengupta
Human Genetics|June 29, 2007
Gene symbol: MYOCKunal Ray, Arijit Mukhopadhyay, Moulinath Acharya
Human Genetics|June 29, 2007
Gene symbol: SLC45A2Kunal Ray, Moumita Chaki, Mainak Sengupta
Human Genetics|June 29, 2007
Gene symbol: SLC45A2Kunal Ray, Moumita Chaki, Mainak Sengupta
Human Genetics|April 3, 2008
Novel human pathological mutations. Gene symbol: TYR. Disease: albinism, oculocutaneous 1Kunal Ray, Moumita Chaki, Mainak Sengupta
Molecular Vision|May 5, 2004
Bioinformatic approaches for identification and characterization of olfactomedin related genes with a potential role in pathogenesis of ocular disordersArijit Mukhopadhyay, Sangita Talukdar, Ashima Bhattacharjee, et al.
Molecular Vision|September 5, 2007
SLC45A2 variations in Indian oculocutaneous albinism patientsMainak Sengupta, Moumita Chaki, N Arti, et al.
Pageof 12

Showing results (21-30 of 113) with videos related to

Sort By:
Pageof 12
Human Genetics|June 29, 2007
Gene symbol: CYP1B1Kunal Ray, Moulinath Acharya, Suddhasil Mookherjee
Human Genetics|June 29, 2007
Gene symbol: CYP1B1Kunal Ray, Moulinath Acharya, Suddhasil Mookherjee
Human Genetics|June 29, 2007
Gene symbol: SLC45A2Kunal Ray, Moumita Chaki, Mainak Sengupta
Human Genetics|April 3, 2008
Novel human pathological mutations. Gene symbol: TYR. Disease: tyrosinase deficiencyKunal Ray, Moumita Chaki, Mainak Sengupta
Human Genetics|June 29, 2007
Gene symbol: MYOCKunal Ray, Arijit Mukhopadhyay, Moulinath Acharya
Human Genetics|June 29, 2007
Gene symbol: SLC45A2Kunal Ray, Moumita Chaki, Mainak Sengupta
Human Genetics|June 29, 2007
Gene symbol: SLC45A2Kunal Ray, Moumita Chaki, Mainak Sengupta
Human Genetics|April 3, 2008
Novel human pathological mutations. Gene symbol: TYR. Disease: albinism, oculocutaneous 1Kunal Ray, Moumita Chaki, Mainak Sengupta
Molecular Vision|May 5, 2004
Bioinformatic approaches for identification and characterization of olfactomedin related genes with a potential role in pathogenesis of ocular disordersArijit Mukhopadhyay, Sangita Talukdar, Ashima Bhattacharjee, et al.
Molecular Vision|September 5, 2007
SLC45A2 variations in Indian oculocutaneous albinism patientsMainak Sengupta, Moumita Chaki, N Arti, et al.
Pageof 12