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B D Gelb

Showing results (71-80 of 76) with videos related to

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Human Molecular Genetics|November 5, 1999
CBFA1 mutation analysis and functional correlation with phenotypic variability in cleidocranial dysplasiaG Zhou, Y Chen, L Zhou, et al.
The Journal of Heart and Lung Transplantation : the Official Publication of the International Society for Heart Transplantation|September 1, 1992
Neurologic complications of heart transplantation in childrenA B Martin, J T Bricker, M Fishman, et al.
The Journal of Clinical Investigation|March 13, 1999
Characterization of novel cathepsin K mutations in the pro and mature polypeptide regions causing pycnodysostosisW S Hou, D Brömme, Y Zhao, et al.
American Journal of Human Genetics|April 25, 2000
Gaucher disease: the origins of the Ashkenazi Jewish N370S and 84GG acid beta-glucosidase mutationsG A Diaz, B D Gelb, N Risch, et al.
Nature Genetics|November 13, 2001
Mutations in PTPN11, encoding the protein tyrosine phosphatase SHP-2, cause Noonan syndromeM Tartaglia, E L Mehler, R Goldberg, et al.
Bioinformatics (Oxford, England)|March 24, 2019
ORE identifies extreme expression effects enriched for rare variantsF Richter, G E Hoffman, K B Manheimer, et al.
Pageof 8

Showing results (71-80 of 76) with videos related to

Sort By:
Pageof 8
You have reached the last page of results.This site can display upto 76 results.
Human Molecular Genetics|November 5, 1999
CBFA1 mutation analysis and functional correlation with phenotypic variability in cleidocranial dysplasiaG Zhou, Y Chen, L Zhou, et al.
The Journal of Heart and Lung Transplantation : the Official Publication of the International Society for Heart Transplantation|September 1, 1992
Neurologic complications of heart transplantation in childrenA B Martin, J T Bricker, M Fishman, et al.
The Journal of Clinical Investigation|March 13, 1999
Characterization of novel cathepsin K mutations in the pro and mature polypeptide regions causing pycnodysostosisW S Hou, D Brömme, Y Zhao, et al.
American Journal of Human Genetics|April 25, 2000
Gaucher disease: the origins of the Ashkenazi Jewish N370S and 84GG acid beta-glucosidase mutationsG A Diaz, B D Gelb, N Risch, et al.
Nature Genetics|November 13, 2001
Mutations in PTPN11, encoding the protein tyrosine phosphatase SHP-2, cause Noonan syndromeM Tartaglia, E L Mehler, R Goldberg, et al.
Bioinformatics (Oxford, England)|March 24, 2019
ORE identifies extreme expression effects enriched for rare variantsF Richter, G E Hoffman, K B Manheimer, et al.
Pageof 8