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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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G L Feldman

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Surgery|July 6, 2000

Variable expressivity of familial medullary thyroid carcinoma (FMTC) due to a RET V804M (GTG-->ATG) mutationG L Feldman, M W Edmonds, P J Ainsworth, 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.

Prenatal Diagnosis|December 11, 1999

Satellited chromosome 10 detected prenatally in a fetus and confirmed as mosaic in a parentP D Storto, T N Diehn, D P O'Malley, et al.

Cancer Research|August 1, 1996

Familial predisposition to neuroblastoma does not map to chromosome band 1p36J M Maris, S M Kyemba, T R Rebbeck, et al.

Neuromuscular Disorders : NMD|May 5, 1998

Beta-sarcoglycan: genomic analysis and identification of a novel missense mutation in the LGMD2E Amish isolateF Duclos, O Broux, N Bourg, et al.

American Journal of Human Genetics|March 21, 2000

Survey of the fragile X syndrome CGG repeat and the short-tandem-repeat and single-nucleotide-polymorphism haplotypes in an African American populationD C Crawford, C E Schwartz, K L Meadows, et al.

Pageof 6

Search research articles

Showing results (51-60 of 56) with videos related to

Sort By:

Pageof 6

You have reached the last page of results.This site can display upto 56 results.

Surgery|July 6, 2000

Variable expressivity of familial medullary thyroid carcinoma (FMTC) due to a RET V804M (GTG-->ATG) mutationG L Feldman, M W Edmonds, P J Ainsworth, 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.

Prenatal Diagnosis|December 11, 1999

Satellited chromosome 10 detected prenatally in a fetus and confirmed as mosaic in a parentP D Storto, T N Diehn, D P O'Malley, et al.

Cancer Research|August 1, 1996

Familial predisposition to neuroblastoma does not map to chromosome band 1p36J M Maris, S M Kyemba, T R Rebbeck, et al.

Neuromuscular Disorders : NMD|May 5, 1998

Beta-sarcoglycan: genomic analysis and identification of a novel missense mutation in the LGMD2E Amish isolateF Duclos, O Broux, N Bourg, et al.

American Journal of Human Genetics|March 21, 2000

Survey of the fragile X syndrome CGG repeat and the short-tandem-repeat and single-nucleotide-polymorphism haplotypes in an African American populationD C Crawford, C E Schwartz, K L Meadows, et al.

Pageof 6