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Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences
|
November 29, 1995
The role of SOX9 in autosomal sex reversal and campomelic dysplasia
A J Schafer, M A Dominguez-Steglich, S Guioli, et al.
Neurogenetics
|
May 18, 1999
HLA typing in the United Kingdom multiple sclerosis genome screen
F Coraddu, S Sawcer, R Feakes, et al.
Annals of Human Genetics
|
July 1, 1981
Deficiency of malic enzyme: a possible marker for malignancy in lymphoid cells
S Povey, S Jeremiah, E Arthur, et al.
Journal of Neuroimmunology
|
September 25, 1999
No evidence for association of multiple sclerosis with the complement factors C6 and C7
J Chataway, S Sawcer, D Sherman, et al.
The Journal of Clinical Endocrinology and Metabolism
|
March 1, 1993
The role of the sex-determining region Y gene in the etiology of 46,XX maleness
P Y Fechner, S M Marcantonio, V Jaswaney, et al.
Genomics
|
April 15, 1996
A high-resolution whole genome radiation hybrid map of human chromosome 17q22-q25.3 across the genes for GH and TK
J W Foster, A J Schafer, R Critcher, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society
|
September 1, 2000
A horse whole-genome-radiation hybrid panel: chromosome 1 and 10 preliminary maps
S L Kiguwa, P Hextall, A L Smith, et al.
Nature
|
October 8, 1992
Evolution of sex determination and the Y chromosome: SRY-related sequences in marsupials
J W Foster, F E Brennan, G K Hampikian, et al.
Nature
|
July 19, 1990
A gene from the human sex-determining region encodes a protein with homology to a conserved DNA-binding motif
A H Sinclair, P Berta, M S Palmer, et al.
Human Molecular Genetics
|
March 1, 1996
A radiation hybrid map of the human genome
G Gyapay, K Schmitt, C Fizames, et al.
Page
of 22
Search research articles
Search
Showing results (201-210 of 214) with videos related to
Sort By:
Page
of 22
Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences
|
November 29, 1995
The role of SOX9 in autosomal sex reversal and campomelic dysplasia
A J Schafer, M A Dominguez-Steglich, S Guioli, et al.
Neurogenetics
|
May 18, 1999
HLA typing in the United Kingdom multiple sclerosis genome screen
F Coraddu, S Sawcer, R Feakes, et al.
Annals of Human Genetics
|
July 1, 1981
Deficiency of malic enzyme: a possible marker for malignancy in lymphoid cells
S Povey, S Jeremiah, E Arthur, et al.
Journal of Neuroimmunology
|
September 25, 1999
No evidence for association of multiple sclerosis with the complement factors C6 and C7
J Chataway, S Sawcer, D Sherman, et al.
The Journal of Clinical Endocrinology and Metabolism
|
March 1, 1993
The role of the sex-determining region Y gene in the etiology of 46,XX maleness
P Y Fechner, S M Marcantonio, V Jaswaney, et al.
Genomics
|
April 15, 1996
A high-resolution whole genome radiation hybrid map of human chromosome 17q22-q25.3 across the genes for GH and TK
J W Foster, A J Schafer, R Critcher, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society
|
September 1, 2000
A horse whole-genome-radiation hybrid panel: chromosome 1 and 10 preliminary maps
S L Kiguwa, P Hextall, A L Smith, et al.
Nature
|
October 8, 1992
Evolution of sex determination and the Y chromosome: SRY-related sequences in marsupials
J W Foster, F E Brennan, G K Hampikian, et al.
Nature
|
July 19, 1990
A gene from the human sex-determining region encodes a protein with homology to a conserved DNA-binding motif
A H Sinclair, P Berta, M S Palmer, et al.
Human Molecular Genetics
|
March 1, 1996
A radiation hybrid map of the human genome
G Gyapay, K Schmitt, C Fizames, et al.
Page
of 22