A Hajra|F S Collins - JoVE Visualize

Showing results (171-180 of 234) with videos related to

Pageof 24

Sort By:

Journal of Medical Genetics|September 1, 1987

Linkage analysis of peripheral neurofibromatosis to DNA markers on chromosome 8S R Diehl, M Boehnke, F S Collins, et al.

Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|May 1, 1995

Germline BRCA1 mutations and loss of the wild-type allele in tumors from families with early onset breast and ovarian cancerS D Merajver, T S Frank, J Xu, et al.

Cell|September 21, 1990

Correction of the cystic fibrosis defect in vitro by retrovirus-mediated gene transferM L Drumm, H A Pope, W H Cliff, et al.

Nature Genetics|April 1, 1995

Somatic mutations in the BRCA1 gene in sporadic ovarian tumoursS D Merajver, T M Pham, R F Caduff, et al.

Genomics|July 1, 1992

A yeast artificial chromosome contig encompassing the type 1 neurofibromatosis geneD A Marchuk, R Tavakkol, M R Wallace, et al.

Genesis (New York, N.Y. : 2000)|September 6, 2001

Bidirectional transcriptional activity of PGK-neomycin and unexpected embryonic lethality in heterozygote chimeric knockout miceP C Scacheri, J S Crabtree, E A Novotny, et al.

The New England Journal of Medicine|February 1, 1990

Mutation analysis for heterozygote detection and the prenatal diagnosis of cystic fibrosisW K Lemna, G L Feldman, B Kerem, et al.

American Journal of Human Genetics|August 1, 1992

A recombination event that redefines the Huntington disease regionR G Snell, L M Thompson, D A Tagle, et al.

Nature Genetics|July 1, 1997

Mutations in the human Jagged1 gene are responsible for Alagille syndromeT Oda, A G Elkahloun, B L Pike, et al.

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.

Pageof 24

Showing results (171-180 of 234) with videos related to

Sort By:

Pageof 24

Journal of Medical Genetics|September 1, 1987

Linkage analysis of peripheral neurofibromatosis to DNA markers on chromosome 8S R Diehl, M Boehnke, F S Collins, et al.

Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|May 1, 1995

Germline BRCA1 mutations and loss of the wild-type allele in tumors from families with early onset breast and ovarian cancerS D Merajver, T S Frank, J Xu, et al.

Cell|September 21, 1990

Correction of the cystic fibrosis defect in vitro by retrovirus-mediated gene transferM L Drumm, H A Pope, W H Cliff, et al.

Nature Genetics|April 1, 1995

Somatic mutations in the BRCA1 gene in sporadic ovarian tumoursS D Merajver, T M Pham, R F Caduff, et al.

Genomics|July 1, 1992

A yeast artificial chromosome contig encompassing the type 1 neurofibromatosis geneD A Marchuk, R Tavakkol, M R Wallace, et al.

Genesis (New York, N.Y. : 2000)|September 6, 2001

Bidirectional transcriptional activity of PGK-neomycin and unexpected embryonic lethality in heterozygote chimeric knockout miceP C Scacheri, J S Crabtree, E A Novotny, et al.

The New England Journal of Medicine|February 1, 1990

Mutation analysis for heterozygote detection and the prenatal diagnosis of cystic fibrosisW K Lemna, G L Feldman, B Kerem, et al.

American Journal of Human Genetics|August 1, 1992

A recombination event that redefines the Huntington disease regionR G Snell, L M Thompson, D A Tagle, et al.

Nature Genetics|July 1, 1997

Mutations in the human Jagged1 gene are responsible for Alagille syndromeT Oda, A G Elkahloun, B L Pike, et al.

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.

Pageof 24