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T E Kelly

Showing results (41-50 of 103) with videos related to

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Clinical Chemistry|March 1, 1990
Muscle enzymes and isoenzymes in Emery-Dreifuss muscular dystrophyM G Bialer, D E Bruns, T E Kelly
Birth Defects Original Article Series|January 1, 1974
Mucolipidosis III (pseudo-Hurler polydystrophy)T E Kelly, C W Reynolds, D C Siggers
Journal of Medical Genetics|August 1, 1986
Secondary amenorrhoea and 47,XX,i(Xq) karyotypeT E Kelly, J W Wilks, H E Wyandt
The Journal of Heredity|January 1, 1975
A 14/14 marker chromosome lymphocyte clone in ataxia telangiectasiaJ M Rary, M A Bender, T E Kelly
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|February 23, 1999
Extension of phenotype associated with structural mutations in type I collagen: siblings with juvenile osteoporosis have an alpha2(I)Gly436 --> Arg substitutionP A Dawson, T E Kelly, J C Marini
Southern Medical Journal|November 1, 1979
Partial trisomy 4q resulting from a familial 4/3 translocationT E Kelly, R H Haslam, G H Thomas
Journal of Medical Genetics|March 1, 1973
Observations suggesting allelism of the achondroplasia and hypochondroplasia genesV A McKusick, T E Kelly, J P Dorst
Digestive Diseases and Sciences|January 1, 1993
Gastrointestinal involvement in a woman with dyskeratosis congenitaK E Brown, T E Kelly, B M Myers
Virginia Medical|June 1, 1982
Homocystinuria: need for early diagnosis and therapyT E Kelly, W G Wilson, E J Squillaro
American Journal of Medical Genetics|May 8, 1999
Chondrodysplasia punctata stemming from maternal lupus erythematosusT E Kelly, B A Alford, K M Greer
Pageof 11

Showing results (41-50 of 103) with videos related to

Sort By:
Pageof 11
Clinical Chemistry|March 1, 1990
Muscle enzymes and isoenzymes in Emery-Dreifuss muscular dystrophyM G Bialer, D E Bruns, T E Kelly
Birth Defects Original Article Series|January 1, 1974
Mucolipidosis III (pseudo-Hurler polydystrophy)T E Kelly, C W Reynolds, D C Siggers
Journal of Medical Genetics|August 1, 1986
Secondary amenorrhoea and 47,XX,i(Xq) karyotypeT E Kelly, J W Wilks, H E Wyandt
The Journal of Heredity|January 1, 1975
A 14/14 marker chromosome lymphocyte clone in ataxia telangiectasiaJ M Rary, M A Bender, T E Kelly
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|February 23, 1999
Extension of phenotype associated with structural mutations in type I collagen: siblings with juvenile osteoporosis have an alpha2(I)Gly436 --> Arg substitutionP A Dawson, T E Kelly, J C Marini
Southern Medical Journal|November 1, 1979
Partial trisomy 4q resulting from a familial 4/3 translocationT E Kelly, R H Haslam, G H Thomas
Journal of Medical Genetics|March 1, 1973
Observations suggesting allelism of the achondroplasia and hypochondroplasia genesV A McKusick, T E Kelly, J P Dorst
Digestive Diseases and Sciences|January 1, 1993
Gastrointestinal involvement in a woman with dyskeratosis congenitaK E Brown, T E Kelly, B M Myers
Virginia Medical|June 1, 1982
Homocystinuria: need for early diagnosis and therapyT E Kelly, W G Wilson, E J Squillaro
American Journal of Medical Genetics|May 8, 1999
Chondrodysplasia punctata stemming from maternal lupus erythematosusT E Kelly, B A Alford, K M Greer
Pageof 11