J M Rommens - JoVE Visualize

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Science (New York, N.Y.)|September 8, 1989

Identification of the cystic fibrosis gene: chromosome walking and jumpingJ M Rommens, M C Iannuzzi, B Kerem, et al.

Human Molecular Genetics|July 1, 1993

A transcription map of the region containing the Huntington disease geneJ M Rommens, B Lin, G B Hutchinson, et al.

Nature|March 25, 1993

Identification of an Alu retrotransposition event in close proximity to a strong candidate gene for Huntington's diseaseY P Goldberg, J M Rommens, S E Andrew, et al.

European Journal of Human Genetics : EJHG|October 22, 1998

Generation of a transcription map of a 1 Mbase region containing the HFE gene (6p22)A Totaro, A Roetto, J M Rommens, et al.

Human Molecular Genetics|July 1, 1997

Translocation breakpoint maps 5 kb 3' from TWIST in a patient affected with Saethre-Chotzen syndromeI Krebs, I Weis, M Hudler, 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.

Human Molecular Genetics|May 1, 1996

Characterization of the split hand/split foot malformation locus SHFM1 at 7q21.3-q22.1 and analysis of a candidate gene for its expression during limb developmentM A Crackower, S W Scherer, J M Rommens, et al.

American Journal of Medical Genetics|July 16, 1999

Exclusion of linkage of Shwachman-Diamond syndrome to chromosome regions 6q and 12q implicated by a de novo translocationS Goobie, J Morrison, H Ginzberg, et al.

Proceedings of the National Academy of Sciences of the United States of America|April 18, 1998

Cloning and mapping of a cDNA for methionine synthase reductase, a flavoprotein defective in patients with homocystinuriaD Leclerc, A Wilson, R Dumas, et al.

The Journal of Pediatrics|July 7, 1999

Shwachman syndrome: phenotypic manifestations of sibling sets and isolated cases in a large patient cohort are similarH Ginzberg, J Shin, L Ellis, et al.

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Showing results (41-50 of 66) with videos related to

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Science (New York, N.Y.)|September 8, 1989

Identification of the cystic fibrosis gene: chromosome walking and jumpingJ M Rommens, M C Iannuzzi, B Kerem, et al.

Human Molecular Genetics|July 1, 1993

A transcription map of the region containing the Huntington disease geneJ M Rommens, B Lin, G B Hutchinson, et al.

Nature|March 25, 1993

Identification of an Alu retrotransposition event in close proximity to a strong candidate gene for Huntington's diseaseY P Goldberg, J M Rommens, S E Andrew, et al.

European Journal of Human Genetics : EJHG|October 22, 1998

Generation of a transcription map of a 1 Mbase region containing the HFE gene (6p22)A Totaro, A Roetto, J M Rommens, et al.

Human Molecular Genetics|July 1, 1997

Translocation breakpoint maps 5 kb 3' from TWIST in a patient affected with Saethre-Chotzen syndromeI Krebs, I Weis, M Hudler, 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.

Human Molecular Genetics|May 1, 1996

Characterization of the split hand/split foot malformation locus SHFM1 at 7q21.3-q22.1 and analysis of a candidate gene for its expression during limb developmentM A Crackower, S W Scherer, J M Rommens, et al.

American Journal of Medical Genetics|July 16, 1999

Exclusion of linkage of Shwachman-Diamond syndrome to chromosome regions 6q and 12q implicated by a de novo translocationS Goobie, J Morrison, H Ginzberg, et al.

Proceedings of the National Academy of Sciences of the United States of America|April 18, 1998

Cloning and mapping of a cDNA for methionine synthase reductase, a flavoprotein defective in patients with homocystinuriaD Leclerc, A Wilson, R Dumas, et al.

The Journal of Pediatrics|July 7, 1999

Shwachman syndrome: phenotypic manifestations of sibling sets and isolated cases in a large patient cohort are similarH Ginzberg, J Shin, L Ellis, et al.

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