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ABOUT JoVE

Overview Leadership Blog JoVE Help Center

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Publishing Process Editorial Board Scope & Policies Peer Review FAQ Submit

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R G Gregg

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American Journal of Human Genetics|July 1, 1993

Genetic heterogeneity in families with hereditary multiple exostosesA Cook, W Raskind, S H Blanton, et al.

Pediatric Pulmonology. Supplement|January 1, 1991

Current issues in neonatal screening for cystic fibrosis and implications of the CF gene discoveryP M Farrell, E H Mischler, N C Fost, et al.

Pediatrics|June 1, 1997

Newborn screening for cystic fibrosis in Wisconsin: comparison of biochemical and molecular methodsR G Gregg, A Simantel, P M Farrell, et al.

Human Molecular Genetics|August 1, 1994

A calcium channel mutation causing hypokalemic periodic paralysisK Jurkat-Rott, F Lehmann-Horn, A Elbaz, et al.

Proceedings of the National Academy of Sciences of the United States of America|June 25, 1996

Targeted deletion in astrocyte intermediate filament (Gfap) alters neuronal physiologyM A McCall, R G Gregg, R R Behringer, et al.

American Journal of Human Genetics|February 1, 1993

Refined genetic localization for central core diseaseJ C Mulley, H M Kozman, H A Phillips, et al.

Human Molecular Genetics|April 6, 2000

Genetic localization of an autosomal dominant leukodystrophy mimicking chronic progressive multiple sclerosis to chromosome 5q31C M Coffeen, C E McKenna, A H Koeppen, et al.

Pageof 6

Search research articles

Showing results (51-60 of 57) with videos related to

Sort By:

Pageof 6

You have reached the last page of results.This site can display upto 57 results.

American Journal of Human Genetics|July 1, 1993

Genetic heterogeneity in families with hereditary multiple exostosesA Cook, W Raskind, S H Blanton, et al.

Pediatric Pulmonology. Supplement|January 1, 1991

Current issues in neonatal screening for cystic fibrosis and implications of the CF gene discoveryP M Farrell, E H Mischler, N C Fost, et al.

Pediatrics|June 1, 1997

Newborn screening for cystic fibrosis in Wisconsin: comparison of biochemical and molecular methodsR G Gregg, A Simantel, P M Farrell, et al.

Human Molecular Genetics|August 1, 1994

A calcium channel mutation causing hypokalemic periodic paralysisK Jurkat-Rott, F Lehmann-Horn, A Elbaz, et al.

Proceedings of the National Academy of Sciences of the United States of America|June 25, 1996

Targeted deletion in astrocyte intermediate filament (Gfap) alters neuronal physiologyM A McCall, R G Gregg, R R Behringer, et al.

American Journal of Human Genetics|February 1, 1993

Refined genetic localization for central core diseaseJ C Mulley, H M Kozman, H A Phillips, et al.

Human Molecular Genetics|April 6, 2000

Genetic localization of an autosomal dominant leukodystrophy mimicking chronic progressive multiple sclerosis to chromosome 5q31C M Coffeen, C E McKenna, A H Koeppen, et al.

Pageof 6