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Showing results (41-50 of 63) with videos related to

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American Journal of Medical Genetics|May 8, 2000
Submicroscopic deletion in cousins with Prader-Willi syndrome causes a grandmatrilineal inheritance pattern: effects of imprintingJ E Ming, N Blagowidow, J H Knoll, et al.
American Journal of Human Genetics|May 1, 1989
The role of cytologic NOR variants in the etiology of trisomy 21N B Spinner, D L Eunpu, R D Schmickel, et al.
Human Molecular Genetics|November 11, 1999
The expression of Jagged1 in the developing mammalian heart correlates with cardiovascular disease in Alagille syndromeK M Loomes, L A Underkoffler, J Morabito, et al.
Human Genetics|April 1, 1996
Ablepharon macrostomia syndrome with associated cutis laxa: possible localization to 18qJ E Pellegrino, R E Schnur, L Boghosian-Sell, et al.
Human Molecular Genetics|November 1, 1994
Diverse mutations of the P gene among African-Americans with type II (tyrosinase-positive) oculocutaneous albinism (OCA2)S T Lee, R D Nicholls, R E Schnur, et al.
Human Genetics|March 10, 1999
Fibroblast growth factor homologous factor 2 (FHF2): gene structure, expression and mapping to the Börjeson-Forssman-Lehmann syndrome region in Xq26 delineated by a duplication breakpoint in a BFLS-like patientJ Gecz, E Baker, A Donnelly, et al.
Genomics|August 1, 1996
Identification, characterization, and chromosomal localization of the human homolog (hES) of ES/130C T Basson, C A MacRae, M Schoenberg-Fejzo, et al.
American Journal of Medical Genetics|May 2, 1997
Deletions of 20p12 in Alagille syndrome: frequency and molecular characterizationI D Krantz, E B Rand, A Genin, et al.
International Journal of Oncology|April 14, 2000
Homozygous deletion of the death receptor DR4 gene in a nasopharyngeal cancer cell line is associated with TRAIL resistanceN Ozören, M J Fisher, K Kim, et al.
Clinical Immunology (Orlando, Fla.)|May 31, 2008
Monosomy 1p36 uncovers a role for OX40 in survival of activated CD4+ T cellsM M Suhoski, E E Perez, M L Heltzer, et al.
Pageof 7

Showing results (41-50 of 63) with videos related to

Sort By:
Pageof 7
American Journal of Medical Genetics|May 8, 2000
Submicroscopic deletion in cousins with Prader-Willi syndrome causes a grandmatrilineal inheritance pattern: effects of imprintingJ E Ming, N Blagowidow, J H Knoll, et al.
American Journal of Human Genetics|May 1, 1989
The role of cytologic NOR variants in the etiology of trisomy 21N B Spinner, D L Eunpu, R D Schmickel, et al.
Human Molecular Genetics|November 11, 1999
The expression of Jagged1 in the developing mammalian heart correlates with cardiovascular disease in Alagille syndromeK M Loomes, L A Underkoffler, J Morabito, et al.
Human Genetics|April 1, 1996
Ablepharon macrostomia syndrome with associated cutis laxa: possible localization to 18qJ E Pellegrino, R E Schnur, L Boghosian-Sell, et al.
Human Molecular Genetics|November 1, 1994
Diverse mutations of the P gene among African-Americans with type II (tyrosinase-positive) oculocutaneous albinism (OCA2)S T Lee, R D Nicholls, R E Schnur, et al.
Human Genetics|March 10, 1999
Fibroblast growth factor homologous factor 2 (FHF2): gene structure, expression and mapping to the Börjeson-Forssman-Lehmann syndrome region in Xq26 delineated by a duplication breakpoint in a BFLS-like patientJ Gecz, E Baker, A Donnelly, et al.
Genomics|August 1, 1996
Identification, characterization, and chromosomal localization of the human homolog (hES) of ES/130C T Basson, C A MacRae, M Schoenberg-Fejzo, et al.
American Journal of Medical Genetics|May 2, 1997
Deletions of 20p12 in Alagille syndrome: frequency and molecular characterizationI D Krantz, E B Rand, A Genin, et al.
International Journal of Oncology|April 14, 2000
Homozygous deletion of the death receptor DR4 gene in a nasopharyngeal cancer cell line is associated with TRAIL resistanceN Ozören, M J Fisher, K Kim, et al.
Clinical Immunology (Orlando, Fla.)|May 31, 2008
Monosomy 1p36 uncovers a role for OX40 in survival of activated CD4+ T cellsM M Suhoski, E E Perez, M L Heltzer, et al.
Pageof 7