M R Wallace|D G Hooper - JoVE Visualize

Showing results (51-60 of 165) with videos related to

Pageof 17

Sort By:

Human Mutation|January 1, 1994

Two NF1 mutations: frameshift in the GAP-related domain, and loss of two codons toward the 3' end of the geneC R Abernathy, S D Colman, B G Kousseff, et al.

Acta Haematologica|January 1, 1984

Hemorrhagic diathesis in multiple myelomaM R Wallace, S R Simon, W B Ershler, et al.

Genomics|June 1, 1990

Human chromosome 17 NotI linking clones and their use in long-range restriction mapping of the Miller-Dieker chromosome region (MDCR) in 17p13.3S A Ledbetter, M R Wallace, F S Collins, et al.

American Journal of Medical Genetics|October 1, 1986

Molecular detection of carriers of hereditary amyloidosis in a Swedish-American familyM R Wallace, P M Conneally, G L Long, et al.

Current Drug Targets. Infectious Disorders|November 29, 2002

The strategy of immunologic control of HIV-1 with structured treatment interruptions (STIs)R B Moss, F C Jensen, D J Carlo, et al.

Annals of Internal Medicine|September 25, 1999

Efficacy of influenza vaccination in HIV-infected persons. A randomized, double-blind, placebo-controlled trialS A Tasker, J J Treanor, W B Paxton, et al.

Nucleic Acids Research|February 25, 1989

Direct construction of a chromosome-specific NotI linking library from flow-sorted chromosomesM R Wallace, J W Fountain, A M Brereton, et al.

Journal of Medical Genetics|August 3, 2005

Genetic linkage of a novel autosomal dominant restrictive cardiomyopathy locusJ Zhang, A Kumar, L Kaplan, et al.

Arthritis and Rheumatism|February 1, 1987

Hereditary amyloidosis: description of a new American kindred with late onset cardiomyopathy. Appalachian amyloidM D Benson, M R Wallace, E Tejada, et al.

The Journal of Clinical Investigation|July 1, 1986

Biochemical and molecular genetic characterization of a new variant prealbumin associated with hereditary amyloidosisM R Wallace, F E Dwulet, P M Conneally, et al.

Pageof 17

Showing results (51-60 of 165) with videos related to

Sort By:

Pageof 17

Human Mutation|January 1, 1994

Two NF1 mutations: frameshift in the GAP-related domain, and loss of two codons toward the 3' end of the geneC R Abernathy, S D Colman, B G Kousseff, et al.

Acta Haematologica|January 1, 1984

Hemorrhagic diathesis in multiple myelomaM R Wallace, S R Simon, W B Ershler, et al.

Genomics|June 1, 1990

Human chromosome 17 NotI linking clones and their use in long-range restriction mapping of the Miller-Dieker chromosome region (MDCR) in 17p13.3S A Ledbetter, M R Wallace, F S Collins, et al.

American Journal of Medical Genetics|October 1, 1986

Molecular detection of carriers of hereditary amyloidosis in a Swedish-American familyM R Wallace, P M Conneally, G L Long, et al.

Current Drug Targets. Infectious Disorders|November 29, 2002

The strategy of immunologic control of HIV-1 with structured treatment interruptions (STIs)R B Moss, F C Jensen, D J Carlo, et al.

Annals of Internal Medicine|September 25, 1999

Efficacy of influenza vaccination in HIV-infected persons. A randomized, double-blind, placebo-controlled trialS A Tasker, J J Treanor, W B Paxton, et al.

Nucleic Acids Research|February 25, 1989

Direct construction of a chromosome-specific NotI linking library from flow-sorted chromosomesM R Wallace, J W Fountain, A M Brereton, et al.

Journal of Medical Genetics|August 3, 2005

Genetic linkage of a novel autosomal dominant restrictive cardiomyopathy locusJ Zhang, A Kumar, L Kaplan, et al.

Arthritis and Rheumatism|February 1, 1987

Hereditary amyloidosis: description of a new American kindred with late onset cardiomyopathy. Appalachian amyloidM D Benson, M R Wallace, E Tejada, et al.

The Journal of Clinical Investigation|July 1, 1986

Biochemical and molecular genetic characterization of a new variant prealbumin associated with hereditary amyloidosisM R Wallace, F E Dwulet, P M Conneally, et al.

Pageof 17