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American Journal of Human Genetics
|
August 9, 2003
Miller-Dieker syndrome: analysis of a human contiguous gene syndrome in the mouse
Jessica Yingling, Kazuhito Toyo-Oka, Anthony Wynshaw-Boris
American Journal of Human Genetics
|
May 13, 2003
A neutral explanation for the correlation of diversity with recombination rates in humans
Ines Hellmann, Ingo Ebersberger, Susan E Ptak, et al.
American Journal of Human Genetics
|
July 5, 2003
Linkage disequilibrium and inference of ancestral recombination in 538 single-nucleotide polymorphism clusters across the human genome
Andrew G Clark, Rasmus Nielsen, James Signorovitch, et al.
American Journal of Human Genetics
|
July 10, 2003
The International Psoriasis Genetics Study: assessing linkage to 14 candidate susceptibility loci in a cohort of 942 affected sib pairs
American Journal of Human Genetics
|
October 1, 1992
SSCP and segregation analysis of the human type X collagen gene (COL10A1) in heritable forms of chondrodysplasia
W A Sweetman, B Rash, B Sykes, et al.
American Journal of Human Genetics
|
August 16, 2003
An integrated haplotype map of the human major histocompatibility complex
Emily C Walsh, Kristie A Mather, Stephen F Schaffner, et al.
American Journal of Human Genetics
|
September 16, 2003
Mutations in capillary morphogenesis gene-2 result in the allelic disorders juvenile hyaline fibromatosis and infantile systemic hyalinosis
Oonagh Dowling, Analisa Difeo, Maria C Ramirez, et al.
American Journal of Human Genetics
|
July 1, 1976
Cytogenetic darkroom magic: now you see them, now you don't
K M Overton, R E Magenis, T Brady, et al.
American Journal of Human Genetics
|
December 1, 1992
Genetic and radiation hybrid mapping of the hyperekplexia region on chromosome 5q
S G Ryan, M J Dixon, M A Nigro, et al.
American Journal of Human Genetics
|
August 6, 2003
The paternal-age effect in Apert syndrome is due, in part, to the increased frequency of mutations in sperm
Rivka L Glaser, Karl W Broman, Rebecca L Schulman, et al.
Page
of 1,201
Search research articles
Search
Showing results (1-10 of 12,002) with videos related to
Sort By:
Page
of 1,201
American Journal of Human Genetics
|
August 9, 2003
Miller-Dieker syndrome: analysis of a human contiguous gene syndrome in the mouse
Jessica Yingling, Kazuhito Toyo-Oka, Anthony Wynshaw-Boris
American Journal of Human Genetics
|
May 13, 2003
A neutral explanation for the correlation of diversity with recombination rates in humans
Ines Hellmann, Ingo Ebersberger, Susan E Ptak, et al.
American Journal of Human Genetics
|
July 5, 2003
Linkage disequilibrium and inference of ancestral recombination in 538 single-nucleotide polymorphism clusters across the human genome
Andrew G Clark, Rasmus Nielsen, James Signorovitch, et al.
American Journal of Human Genetics
|
July 10, 2003
The International Psoriasis Genetics Study: assessing linkage to 14 candidate susceptibility loci in a cohort of 942 affected sib pairs
American Journal of Human Genetics
|
October 1, 1992
SSCP and segregation analysis of the human type X collagen gene (COL10A1) in heritable forms of chondrodysplasia
W A Sweetman, B Rash, B Sykes, et al.
American Journal of Human Genetics
|
August 16, 2003
An integrated haplotype map of the human major histocompatibility complex
Emily C Walsh, Kristie A Mather, Stephen F Schaffner, et al.
American Journal of Human Genetics
|
September 16, 2003
Mutations in capillary morphogenesis gene-2 result in the allelic disorders juvenile hyaline fibromatosis and infantile systemic hyalinosis
Oonagh Dowling, Analisa Difeo, Maria C Ramirez, et al.
American Journal of Human Genetics
|
July 1, 1976
Cytogenetic darkroom magic: now you see them, now you don't
K M Overton, R E Magenis, T Brady, et al.
American Journal of Human Genetics
|
December 1, 1992
Genetic and radiation hybrid mapping of the hyperekplexia region on chromosome 5q
S G Ryan, M J Dixon, M A Nigro, et al.
American Journal of Human Genetics
|
August 6, 2003
The paternal-age effect in Apert syndrome is due, in part, to the increased frequency of mutations in sperm
Rivka L Glaser, Karl W Broman, Rebecca L Schulman, et al.
Page
of 1,201