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F S Collins

Showing results (241-250 of 297) with videos related to

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Proceedings of the National Academy of Sciences of the United States of America|October 1, 1989
Chromosomal jumping from the DXS165 locus allows molecular characterization of four microdeletions and a de novo chromosome X/13 translocation associated with choroideremiaF P Cremers, D J van de Pol, B Wieringa, et al.
Science (New York, N.Y.)|June 2, 1989
Physical mapping of a translocation breakpoint in neurofibromatosisJ W Fountain, M R Wallace, M A Bruce, et al.
Nucleic Acids Research|April 11, 1990
D21S194, a jump clone from D21S16A P Walker, F S Collins, T Siddique, et al.
Genomics|July 1, 1994
Physical localization of microsatellite markers at the ataxia-telangiectasia locus at 11q22-q23L Vanagaite, K Savitsky, G Rotman, et al.
Human Mutation|January 1, 1997
Identification of a splice site mutation (2789 +5 G > A) associated with small amounts of normal CFTR mRNA and mild cystic fibrosisW E Highsmith, L H Burch, Z Zhou, et al.
Oncogene|August 30, 2001
The tumor suppressor protein menin interacts with NF-kappaB proteins and inhibits NF-kappaB-mediated transactivationC Heppner, K Y Bilimoria, S K Agarwal, et al.
Genome Research|July 4, 2001
Linkage disequilibrium between microsatellite markers extends beyond 1 cM on chromosome 20 in FinnsK L Mohlke, E M Lange, T T Valle, et al.
Human Genetics|April 1, 1995
A high-density microsatellite map of the ataxia-telangiectasia locusL Vanagaite, M R James, G Rotman, et al.
JAMA|October 23, 1997
Characteristics of prostate cancer in families potentially linked to the hereditary prostate cancer 1 (HPC1) locusH Grönberg, S D Isaacs, J R Smith, et al.
Human Mutation|April 17, 1999
Analysis of CpG C-to-T mutations in neurofibromatosis type 1. Mutations in brief no. 129. OnlineS Krkljus, C R Abernathy, J S Johnson, et al.
Pageof 30

Showing results (241-250 of 297) with videos related to

Sort By:
Pageof 30
Proceedings of the National Academy of Sciences of the United States of America|October 1, 1989
Chromosomal jumping from the DXS165 locus allows molecular characterization of four microdeletions and a de novo chromosome X/13 translocation associated with choroideremiaF P Cremers, D J van de Pol, B Wieringa, et al.
Science (New York, N.Y.)|June 2, 1989
Physical mapping of a translocation breakpoint in neurofibromatosisJ W Fountain, M R Wallace, M A Bruce, et al.
Nucleic Acids Research|April 11, 1990
D21S194, a jump clone from D21S16A P Walker, F S Collins, T Siddique, et al.
Genomics|July 1, 1994
Physical localization of microsatellite markers at the ataxia-telangiectasia locus at 11q22-q23L Vanagaite, K Savitsky, G Rotman, et al.
Human Mutation|January 1, 1997
Identification of a splice site mutation (2789 +5 G > A) associated with small amounts of normal CFTR mRNA and mild cystic fibrosisW E Highsmith, L H Burch, Z Zhou, et al.
Oncogene|August 30, 2001
The tumor suppressor protein menin interacts with NF-kappaB proteins and inhibits NF-kappaB-mediated transactivationC Heppner, K Y Bilimoria, S K Agarwal, et al.
Genome Research|July 4, 2001
Linkage disequilibrium between microsatellite markers extends beyond 1 cM on chromosome 20 in FinnsK L Mohlke, E M Lange, T T Valle, et al.
Human Genetics|April 1, 1995
A high-density microsatellite map of the ataxia-telangiectasia locusL Vanagaite, M R James, G Rotman, et al.
JAMA|October 23, 1997
Characteristics of prostate cancer in families potentially linked to the hereditary prostate cancer 1 (HPC1) locusH Grönberg, S D Isaacs, J R Smith, et al.
Human Mutation|April 17, 1999
Analysis of CpG C-to-T mutations in neurofibromatosis type 1. Mutations in brief no. 129. OnlineS Krkljus, C R Abernathy, J S Johnson, et al.
Pageof 30