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M S Gross

Showing results (61-70 of 72) with videos related to

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U.S. Healthcare|January 9, 1989
Consultant forum ... the future of information and communications systemsB Hudson, A Kaskiw, R D Helppie, et al.
U.S. Healthcare|December 10, 1988
Consultant forum--the future of information and communication systemsA Kaskiw, R D Helpie, R J Feldman, et al.
American Journal of Human Genetics|May 1, 1982
Assignment of the human pro alpha 2(I) collagen structural gene (COLIA2) to chromosome 7 by molecular hybridizationC Junien, D Weil, J C Myers, et al.
Cytogenetics and Cell Genetics|January 1, 1989
Chromosomal assignment of 14 genomic probes for highly polymorphic lociO Cohen-Haguenauer, Nguyen Van Cong, R G Knowlton, et al.
Annales De Genetique|January 1, 1986
Panel of twenty-five independent man-rodent hybrids for human genetic marker mappingNguyen Van Cong, D Weil, C Finaz, et al.
Human Genetics|January 1, 1988
Assignment of the human fast skeletal muscle myosin alkali light chains gene (MLC1F/MLC3F) to 2q 32.1-2qterO Cohen-Haguenauer, P J Barton, V C Nguyen, et al.
Journal of Immunology (Baltimore, Md. : 1950)|June 15, 1995
Neutralizing murine monoclonal antibodies to human IL-5 isolated from hybridomas and a filamentous phage Fab display libraryR S Ames, M A Tornetta, L J McMillan, et al.
The Journal of Clinical Investigation|October 14, 1998
Paternal mutation of the sulfonylurea receptor (SUR1) gene and maternal loss of 11p15 imprinted genes lead to persistent hyperinsulinism in focal adenomatous hyperplasiaV Verkarre, J C Fournet, P de Lonlay, et al.
The American Journal of Pathology|June 8, 2001
Unbalanced expression of 11p15 imprinted genes in focal forms of congenital hyperinsulinism: association with a reduction to homozygosity of a mutation in ABCC8 or KCNJ11J C Fournet, C Mayaud, P de Lonlay, et al.
The Journal of Clinical Investigation|August 15, 1997
Somatic deletion of the imprinted 11p15 region in sporadic persistent hyperinsulinemic hypoglycemia of infancy is specific of focal adenomatous hyperplasia and endorses partial pancreatectomyP de Lonlay, J C Fournet, J Rahier, et al.
Pageof 8

Showing results (61-70 of 72) with videos related to

Sort By:
Pageof 8
U.S. Healthcare|January 9, 1989
Consultant forum ... the future of information and communications systemsB Hudson, A Kaskiw, R D Helppie, et al.
U.S. Healthcare|December 10, 1988
Consultant forum--the future of information and communication systemsA Kaskiw, R D Helpie, R J Feldman, et al.
American Journal of Human Genetics|May 1, 1982
Assignment of the human pro alpha 2(I) collagen structural gene (COLIA2) to chromosome 7 by molecular hybridizationC Junien, D Weil, J C Myers, et al.
Cytogenetics and Cell Genetics|January 1, 1989
Chromosomal assignment of 14 genomic probes for highly polymorphic lociO Cohen-Haguenauer, Nguyen Van Cong, R G Knowlton, et al.
Annales De Genetique|January 1, 1986
Panel of twenty-five independent man-rodent hybrids for human genetic marker mappingNguyen Van Cong, D Weil, C Finaz, et al.
Human Genetics|January 1, 1988
Assignment of the human fast skeletal muscle myosin alkali light chains gene (MLC1F/MLC3F) to 2q 32.1-2qterO Cohen-Haguenauer, P J Barton, V C Nguyen, et al.
Journal of Immunology (Baltimore, Md. : 1950)|June 15, 1995
Neutralizing murine monoclonal antibodies to human IL-5 isolated from hybridomas and a filamentous phage Fab display libraryR S Ames, M A Tornetta, L J McMillan, et al.
The Journal of Clinical Investigation|October 14, 1998
Paternal mutation of the sulfonylurea receptor (SUR1) gene and maternal loss of 11p15 imprinted genes lead to persistent hyperinsulinism in focal adenomatous hyperplasiaV Verkarre, J C Fournet, P de Lonlay, et al.
The American Journal of Pathology|June 8, 2001
Unbalanced expression of 11p15 imprinted genes in focal forms of congenital hyperinsulinism: association with a reduction to homozygosity of a mutation in ABCC8 or KCNJ11J C Fournet, C Mayaud, P de Lonlay, et al.
The Journal of Clinical Investigation|August 15, 1997
Somatic deletion of the imprinted 11p15 region in sporadic persistent hyperinsulinemic hypoglycemia of infancy is specific of focal adenomatous hyperplasia and endorses partial pancreatectomyP de Lonlay, J C Fournet, J Rahier, et al.
Pageof 8