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N B Spinner

Showing results (21-30 of 63) with videos related to

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Journal of Medical Genetics|December 20, 2003
Consequences of JAG1 mutationsB M Kamath, L Bason, D A Piccoli, et al.
Clinical Genetics|December 1, 1993
De novo interstitial deletion of the long arm of chromosome 3: 46,XX,del(3)(q25.1q26.1)N H Robin, M Magnusson, D McDonald-McGinn, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 17, 1999
Unique forms of human and mouse nuclear receptor corepressor SMRTP Ordentlich, M Downes, W Xie, et al.
American Journal of Diseases of Children (1960)|November 1, 1993
Velo-cardio-facial syndrome. Intrafamilial variability of the phenotypeS D McLean, H M Saal, N B Spinner, et al.
Blood|May 1, 1986
A chromosomal breakage syndrome with profound immunodeficiencyM E Conley, N B Spinner, B S Emanuel, et al.
Genomics|August 1, 1997
Cloning, human chromosomal assignment, and adipose and hepatic expression of the CL-6/INSIG1 geneY Peng, E J Schwarz, M A Lazar, et al.
American Journal of Medical Genetics|February 2, 1996
Developmental profile in a patient with monosomy 10q and dup(17p) associated with a peripheral neuropathyJ E Pellegrino, L Pellegrino, N B Spinner, et al.
Human Mutation|January 4, 2001
Jagged1 mutations in alagille syndromeN B Spinner, R P Colliton, C Crosnier, et al.
American Journal of Medical Genetics|February 15, 2001
Boy with bilateral retinoblastoma due to an unusual ring chromosome 13 with activation of a latent centromereJ D Morrissette, L Celle, N L Owens, et al.
Hepatology (Baltimore, Md.)|March 3, 1999
Features of Alagille syndrome in 92 patients: frequency and relation to prognosisK M Emerick, E B Rand, E Goldmuntz, et al.
Pageof 7

Showing results (21-30 of 63) with videos related to

Sort By:
Pageof 7
Journal of Medical Genetics|December 20, 2003
Consequences of JAG1 mutationsB M Kamath, L Bason, D A Piccoli, et al.
Clinical Genetics|December 1, 1993
De novo interstitial deletion of the long arm of chromosome 3: 46,XX,del(3)(q25.1q26.1)N H Robin, M Magnusson, D McDonald-McGinn, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 17, 1999
Unique forms of human and mouse nuclear receptor corepressor SMRTP Ordentlich, M Downes, W Xie, et al.
American Journal of Diseases of Children (1960)|November 1, 1993
Velo-cardio-facial syndrome. Intrafamilial variability of the phenotypeS D McLean, H M Saal, N B Spinner, et al.
Blood|May 1, 1986
A chromosomal breakage syndrome with profound immunodeficiencyM E Conley, N B Spinner, B S Emanuel, et al.
Genomics|August 1, 1997
Cloning, human chromosomal assignment, and adipose and hepatic expression of the CL-6/INSIG1 geneY Peng, E J Schwarz, M A Lazar, et al.
American Journal of Medical Genetics|February 2, 1996
Developmental profile in a patient with monosomy 10q and dup(17p) associated with a peripheral neuropathyJ E Pellegrino, L Pellegrino, N B Spinner, et al.
Human Mutation|January 4, 2001
Jagged1 mutations in alagille syndromeN B Spinner, R P Colliton, C Crosnier, et al.
American Journal of Medical Genetics|February 15, 2001
Boy with bilateral retinoblastoma due to an unusual ring chromosome 13 with activation of a latent centromereJ D Morrissette, L Celle, N L Owens, et al.
Hepatology (Baltimore, Md.)|March 3, 1999
Features of Alagille syndrome in 92 patients: frequency and relation to prognosisK M Emerick, E B Rand, E Goldmuntz, et al.
Pageof 7