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Annals of Human Genetics
|
December 16, 2004
DNA sequence variation and haplotype structure of the ICAM1 and TNF genes in 12 ethnic groups of India reveal patterns of importance in designing association studies
S Sengupta, S Farheen, N Mukherjee, et al.
Genome Research
|
October 1, 1995
An autosomal recessive nonsyndromic form of sensorineural hearing loss maps to 3p-DFNB6
K Fukushima, A Ramesh, C R Srisailapathy, et al.
Human Molecular Genetics
|
March 21, 1998
Localization of a gene for otosclerosis to chromosome 15q25-q26
M S Tomek, M R Brown, S R Mani, et al.
Proteomics
|
February 10, 2016
Proteomic analysis of a compatible interaction between sugarcane and Sporisorium scitamineum
Leonard Barnabas, N M R Ashwin, K Kaverinathan, et al.
Transboundary and Emerging Diseases
|
September 16, 2014
Emergence of Porcine Circovirus 2 Associated Reproductive Failure in Southern India
A K Karuppannan, A Ramesh, Y K Reddy, et al.
Human Mutation
|
May 26, 1998
Identification of mutations in the connexin 26 gene that cause autosomal recessive nonsyndromic hearing loss
D A Scott, M L Kraft, R Carmi, et al.
The Science of the Total Environment
|
May 31, 2024
Bioenergetic mapping of 'healthy microbiomes' via compound processing potential imprinted in gut and soil metagenomes
Craig Liddicoat, Robert A Edwards, Michael Roach, et al.
American Journal of Human Genetics
|
January 10, 2006
Polarity and temporality of high-resolution y-chromosome distributions in India identify both indigenous and exogenous expansions and reveal minor genetic influence of Central Asian pastoralists
Sanghamitra Sengupta, Lev A Zhivotovsky, Roy King, et al.
Genome Research
|
October 6, 1997
Construction of P1-derived artificial chromosome and yeast artificial chromosome contigs encompassing the DFNB7 and DFNB11 region of chromosome 9q13-21
J H Greinwald, D A Scott, J R Marietta, et al.
Human Molecular Genetics
|
June 9, 1998
Two frequent missense mutations in Pendred syndrome
P Van Hauwe, L A Everett, P Coucke, et al.
Page
of 23
Search research articles
Search
Showing results (211-220 of 227) with videos related to
Sort By:
Page
of 23
Annals of Human Genetics
|
December 16, 2004
DNA sequence variation and haplotype structure of the ICAM1 and TNF genes in 12 ethnic groups of India reveal patterns of importance in designing association studies
S Sengupta, S Farheen, N Mukherjee, et al.
Genome Research
|
October 1, 1995
An autosomal recessive nonsyndromic form of sensorineural hearing loss maps to 3p-DFNB6
K Fukushima, A Ramesh, C R Srisailapathy, et al.
Human Molecular Genetics
|
March 21, 1998
Localization of a gene for otosclerosis to chromosome 15q25-q26
M S Tomek, M R Brown, S R Mani, et al.
Proteomics
|
February 10, 2016
Proteomic analysis of a compatible interaction between sugarcane and Sporisorium scitamineum
Leonard Barnabas, N M R Ashwin, K Kaverinathan, et al.
Transboundary and Emerging Diseases
|
September 16, 2014
Emergence of Porcine Circovirus 2 Associated Reproductive Failure in Southern India
A K Karuppannan, A Ramesh, Y K Reddy, et al.
Human Mutation
|
May 26, 1998
Identification of mutations in the connexin 26 gene that cause autosomal recessive nonsyndromic hearing loss
D A Scott, M L Kraft, R Carmi, et al.
The Science of the Total Environment
|
May 31, 2024
Bioenergetic mapping of 'healthy microbiomes' via compound processing potential imprinted in gut and soil metagenomes
Craig Liddicoat, Robert A Edwards, Michael Roach, et al.
American Journal of Human Genetics
|
January 10, 2006
Polarity and temporality of high-resolution y-chromosome distributions in India identify both indigenous and exogenous expansions and reveal minor genetic influence of Central Asian pastoralists
Sanghamitra Sengupta, Lev A Zhivotovsky, Roy King, et al.
Genome Research
|
October 6, 1997
Construction of P1-derived artificial chromosome and yeast artificial chromosome contigs encompassing the DFNB7 and DFNB11 region of chromosome 9q13-21
J H Greinwald, D A Scott, J R Marietta, et al.
Human Molecular Genetics
|
June 9, 1998
Two frequent missense mutations in Pendred syndrome
P Van Hauwe, L A Everett, P Coucke, et al.
Page
of 23