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Proceedings of the National Academy of Sciences of the United States of America
|
December 11, 1991
Toward an animal model of cystic fibrosis: targeted interruption of exon 10 of the cystic fibrosis transmembrane regulator gene in embryonic stem cells
B H Koller, H S Kim, A M Latour, et al.
Genome Research
|
October 6, 1999
Duplications on human chromosome 22 reveal a novel Ret Finger Protein-like gene family with sense and endogenous antisense transcripts
E Seroussi, D Kedra, H Q Pan, et al.
American Journal of Human Genetics
|
June 1, 1995
Molecular definition of the 22q11 deletions in velo-cardio-facial syndrome
B Morrow, R Goldberg, C Carlson, et al.
Nucleic Acids Research
|
November 11, 1986
Genetic homogeneity of cystic fibrosis
K Klinger, P Stanislovitis, N Hoffman, et al.
European Journal of Human Genetics : EJHG
|
August 31, 2001
Replication and extension studies of inflammatory bowel disease susceptibility regions confirm linkage to chromosome 6p (IBD3)
B Dechairo, C Dimon, D van Heel, et al.
Nature Genetics
|
August 1, 1996
A common region of 10p deleted in DiGeorge and velocardiofacial syndromes
S C Daw, C Taylor, M Kraman, et al.
Lancet (London, England)
|
June 21, 1986
First-trimester prenatal diagnosis of cystic fibrosis with linked DNA probes
M Farrall, H Y Law, C H Rodeck, et al.
Clinical Genetics
|
June 11, 1999
Partial DiGeorge syndrome in two patients with a 10p rearrangement
H Van Esch, P Groenen, S Daw, et al.
Human Genetics
|
January 1, 1985
Linkage relationships of the gene for apolipoprotein CII with loci on chromosome 19
J A Donald, S C Wallis, A Kessling, et al.
Nature
|
August 13, 1987
Localization of the gene for familial adenomatous polyposis on chromosome 5
W F Bodmer, C J Bailey, J Bodmer, et al.
Page
of 6
Search research articles
Search
Showing results (41-50 of 58) with videos related to
Sort By:
Page
of 6
Proceedings of the National Academy of Sciences of the United States of America
|
December 11, 1991
Toward an animal model of cystic fibrosis: targeted interruption of exon 10 of the cystic fibrosis transmembrane regulator gene in embryonic stem cells
B H Koller, H S Kim, A M Latour, et al.
Genome Research
|
October 6, 1999
Duplications on human chromosome 22 reveal a novel Ret Finger Protein-like gene family with sense and endogenous antisense transcripts
E Seroussi, D Kedra, H Q Pan, et al.
American Journal of Human Genetics
|
June 1, 1995
Molecular definition of the 22q11 deletions in velo-cardio-facial syndrome
B Morrow, R Goldberg, C Carlson, et al.
Nucleic Acids Research
|
November 11, 1986
Genetic homogeneity of cystic fibrosis
K Klinger, P Stanislovitis, N Hoffman, et al.
European Journal of Human Genetics : EJHG
|
August 31, 2001
Replication and extension studies of inflammatory bowel disease susceptibility regions confirm linkage to chromosome 6p (IBD3)
B Dechairo, C Dimon, D van Heel, et al.
Nature Genetics
|
August 1, 1996
A common region of 10p deleted in DiGeorge and velocardiofacial syndromes
S C Daw, C Taylor, M Kraman, et al.
Lancet (London, England)
|
June 21, 1986
First-trimester prenatal diagnosis of cystic fibrosis with linked DNA probes
M Farrall, H Y Law, C H Rodeck, et al.
Clinical Genetics
|
June 11, 1999
Partial DiGeorge syndrome in two patients with a 10p rearrangement
H Van Esch, P Groenen, S Daw, et al.
Human Genetics
|
January 1, 1985
Linkage relationships of the gene for apolipoprotein CII with loci on chromosome 19
J A Donald, S C Wallis, A Kessling, et al.
Nature
|
August 13, 1987
Localization of the gene for familial adenomatous polyposis on chromosome 5
W F Bodmer, C J Bailey, J Bodmer, et al.
Page
of 6