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T E Kelly

Showing results (81-90 of 103) with videos related to

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Southern Medical Journal|December 1, 1988
Cytogenetic studies in couples with recurrent pregnancy lossD Sider, W G Wilson, K Sudduth, et al.
Journal of Medical Genetics|February 26, 2000
Confirmation of the assignment of the Sanjad-Sakati (congenital hypoparathyroidism) syndrome (OMIM 241410) locus to chromosome lq42-43T E Kelly, S Blanton, R Saif, et al.
American Journal of Human Genetics|May 1, 1975
Tay-Sachs disease: high gene frequency in a non-Jewish populationT E Kelly, G A Chase, M M Kaback, et al.
The Journal of Pediatrics|July 1, 1993
Multiple areas of intestinal atresia associated with immunodeficiency and posttransfusion graft-versus-host diseaseM W Walker, M A Lovell, T E Kelly, et al.
The Journal of Biological Chemistry|June 25, 1983
Synthesis of a shortened pro-alpha 2(I) chain and decreased synthesis of pro-alpha 2(I) chains in a proband with osteogenesis imperfectaW J de Wet, T Pihlajaniemi, J Myers, et al.
American Journal of Medical Genetics|October 21, 1999
Spinal muscular atrophy variant with congenital fracturesT E Kelly, K Amoroso, M Ferre, et al.
American Journal of Medical Genetics|January 1, 1978
The Rieger syndromeR J Jorgenson, L S Levin, H E Cross, et al.
Clinical Genetics|January 1, 1973
Mucolipidosis 3 (pseudo-Hurler polydystrophy): cytological and ultrastructural observations of cultured fibroblast cellsH A Taylor, G H Thomas, C S Miller, et al.
Cytogenetics and Cell Genetics|January 1, 1982
Human chromosome 2 rod/ring mosaicism: probable origin by prezygotic breakage and intrachromosomal exchangeH E Wyandt, R Kasprzak, A Lamb, et al.
American Journal of Human Genetics|March 1, 1984
Distal 15q trisomy: phenotypic comparison of nine cases in an extended familyP Schnatterly, K L Bono, M Robinow, et al.
Pageof 11

Showing results (81-90 of 103) with videos related to

Sort By:
Pageof 11
Southern Medical Journal|December 1, 1988
Cytogenetic studies in couples with recurrent pregnancy lossD Sider, W G Wilson, K Sudduth, et al.
Journal of Medical Genetics|February 26, 2000
Confirmation of the assignment of the Sanjad-Sakati (congenital hypoparathyroidism) syndrome (OMIM 241410) locus to chromosome lq42-43T E Kelly, S Blanton, R Saif, et al.
American Journal of Human Genetics|May 1, 1975
Tay-Sachs disease: high gene frequency in a non-Jewish populationT E Kelly, G A Chase, M M Kaback, et al.
The Journal of Pediatrics|July 1, 1993
Multiple areas of intestinal atresia associated with immunodeficiency and posttransfusion graft-versus-host diseaseM W Walker, M A Lovell, T E Kelly, et al.
The Journal of Biological Chemistry|June 25, 1983
Synthesis of a shortened pro-alpha 2(I) chain and decreased synthesis of pro-alpha 2(I) chains in a proband with osteogenesis imperfectaW J de Wet, T Pihlajaniemi, J Myers, et al.
American Journal of Medical Genetics|October 21, 1999
Spinal muscular atrophy variant with congenital fracturesT E Kelly, K Amoroso, M Ferre, et al.
American Journal of Medical Genetics|January 1, 1978
The Rieger syndromeR J Jorgenson, L S Levin, H E Cross, et al.
Clinical Genetics|January 1, 1973
Mucolipidosis 3 (pseudo-Hurler polydystrophy): cytological and ultrastructural observations of cultured fibroblast cellsH A Taylor, G H Thomas, C S Miller, et al.
Cytogenetics and Cell Genetics|January 1, 1982
Human chromosome 2 rod/ring mosaicism: probable origin by prezygotic breakage and intrachromosomal exchangeH E Wyandt, R Kasprzak, A Lamb, et al.
American Journal of Human Genetics|March 1, 1984
Distal 15q trisomy: phenotypic comparison of nine cases in an extended familyP Schnatterly, K L Bono, M Robinow, et al.
Pageof 11