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ABOUT JoVE

Overview Leadership Blog JoVE Help Center

AUTHORS

Publishing Process Editorial Board Scope & Policies Peer Review FAQ Submit

LIBRARIANS

Testimonials Subscriptions Access Resources Library Advisory Board FAQ

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JoVE Journal Methods Collections JoVE Encyclopedia of Experiments Archive

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R D Wegner

Showing results (61-70 of 67) with videos related to

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Blood|September 15, 1995

Classification of Fanconi anemia patients by complementation analysis: evidence for a fifth genetic subtypeH Joenje, J R Lo ten Foe, A B Oostra, et al.

Human Molecular Genetics|April 4, 2001

Functional hemizygosity of PAFAH1B3 due to a PAFAH1B3-CLK2 fusion gene in a female with mental retardation, ataxia and atrophy of the brainH G Nothwang, H G Kim, J Aoki, et al.

Cytogenetic and Genome Research|April 18, 2009

10p11.2 to 10q11.2 is a yet unreported region leading to unbalanced chromosomal abnormalities without phenotypic consequencesT Liehr, M Stumm, R D Wegner, et al.

Human Molecular Genetics|January 15, 1999

Characterization of ATM gene mutations in 66 ataxia telangiectasia familiesN Sandoval, M Platzer, A Rosenthal, et al.

American Journal of Human Genetics|April 17, 1999

The Fanconi anemia group E gene, FANCE, maps to chromosome 6pQ Waisfisz, K Saar, N V Morgan, et al.

Human Molecular Genetics|April 1, 1996

Predominance of null mutations in ataxia-telangiectasiaS Gilad, R Khosravi, D Shkedy, et al.

International Journal of Radiation Biology|December 1, 1994

Genetic haplotyping of ataxia-telangiectasia families localizes the major gene to an approximately 850 kb region on chromosome 11q23.1R A Gatti, E Lange, G Rotman, et al.

Pageof 7

Search research articles

Showing results (61-70 of 67) with videos related to

Sort By:

Pageof 7

You have reached the last page of results.This site can display upto 67 results.

Blood|September 15, 1995

Classification of Fanconi anemia patients by complementation analysis: evidence for a fifth genetic subtypeH Joenje, J R Lo ten Foe, A B Oostra, et al.

Human Molecular Genetics|April 4, 2001

Functional hemizygosity of PAFAH1B3 due to a PAFAH1B3-CLK2 fusion gene in a female with mental retardation, ataxia and atrophy of the brainH G Nothwang, H G Kim, J Aoki, et al.

Cytogenetic and Genome Research|April 18, 2009

10p11.2 to 10q11.2 is a yet unreported region leading to unbalanced chromosomal abnormalities without phenotypic consequencesT Liehr, M Stumm, R D Wegner, et al.

Human Molecular Genetics|January 15, 1999

Characterization of ATM gene mutations in 66 ataxia telangiectasia familiesN Sandoval, M Platzer, A Rosenthal, et al.

American Journal of Human Genetics|April 17, 1999

The Fanconi anemia group E gene, FANCE, maps to chromosome 6pQ Waisfisz, K Saar, N V Morgan, et al.

Human Molecular Genetics|April 1, 1996

Predominance of null mutations in ataxia-telangiectasiaS Gilad, R Khosravi, D Shkedy, et al.

International Journal of Radiation Biology|December 1, 1994

Genetic haplotyping of ataxia-telangiectasia families localizes the major gene to an approximately 850 kb region on chromosome 11q23.1R A Gatti, E Lange, G Rotman, et al.

Pageof 7