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N B Spinner

Showing results (31-40 of 63) with videos related to

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Human Mutation|February 17, 2001
Mutation analysis of Jagged1 (JAG1) in Alagille syndrome patientsR P Colliton, L Bason, F M Lu, et al.
American Journal of Human Genetics|August 1, 1994
Cytologically balanced t(2;20) in a two-generation family with alagille syndrome: cytogenetic and molecular studiesN B Spinner, E B Rand, P Fortina, et al.
Human Mutation|November 3, 2000
Jagged1 (JAG1) mutation detection in an Australian Alagille syndrome populationM L Heritage, J C MacMillan, R P Colliton, et al.
Nature Genetics|September 1, 1997
Epilepsy and mental retardation limited to females: an X-linked dominant disorder with male sparingS G Ryan, P F Chance, C H Zou, et al.
Clinical Genetics|September 20, 2012
Physicians' perspectives on the uncertainties and implications of chromosomal microarray testing of children and familiesM Reiff, K Ross, S Mulchandani, et al.
American Journal of Medical Genetics|March 13, 1995
Mosaicism for a chromosome 8-derived minute marker chromosome in a patient with manifestations of trisomy 8 mosaicismN B Spinner, K R Grace, N L Owens, et al.
American Journal of Medical Genetics|April 1, 1993
46,XX,15p+ documented as dup (17p) by fluorescence in situ hybridizationN B Spinner, J A Biegel, L Sovinsky, et al.
American Journal of Human Genetics|June 19, 1998
Spectrum and frequency of jagged1 (JAG1) mutations in Alagille syndrome patients and their familiesI D Krantz, R P Colliton, A Genin, et al.
Genomics|January 20, 1995
The human osmoregulatory Na+/myo-inositol cotransporter gene (SLC5A3): molecular cloning and localization to chromosome 21G T Berry, J J Mallee, H M Kwon, et al.
American Journal of Medical Genetics|April 23, 1999
Jagged1 mutations in patients ascertained with isolated congenital heart defectsI D Krantz, R Smith, R P Colliton, et al.
Pageof 7

Showing results (31-40 of 63) with videos related to

Sort By:
Pageof 7
Human Mutation|February 17, 2001
Mutation analysis of Jagged1 (JAG1) in Alagille syndrome patientsR P Colliton, L Bason, F M Lu, et al.
American Journal of Human Genetics|August 1, 1994
Cytologically balanced t(2;20) in a two-generation family with alagille syndrome: cytogenetic and molecular studiesN B Spinner, E B Rand, P Fortina, et al.
Human Mutation|November 3, 2000
Jagged1 (JAG1) mutation detection in an Australian Alagille syndrome populationM L Heritage, J C MacMillan, R P Colliton, et al.
Nature Genetics|September 1, 1997
Epilepsy and mental retardation limited to females: an X-linked dominant disorder with male sparingS G Ryan, P F Chance, C H Zou, et al.
Clinical Genetics|September 20, 2012
Physicians' perspectives on the uncertainties and implications of chromosomal microarray testing of children and familiesM Reiff, K Ross, S Mulchandani, et al.
American Journal of Medical Genetics|March 13, 1995
Mosaicism for a chromosome 8-derived minute marker chromosome in a patient with manifestations of trisomy 8 mosaicismN B Spinner, K R Grace, N L Owens, et al.
American Journal of Medical Genetics|April 1, 1993
46,XX,15p+ documented as dup (17p) by fluorescence in situ hybridizationN B Spinner, J A Biegel, L Sovinsky, et al.
American Journal of Human Genetics|June 19, 1998
Spectrum and frequency of jagged1 (JAG1) mutations in Alagille syndrome patients and their familiesI D Krantz, R P Colliton, A Genin, et al.
Genomics|January 20, 1995
The human osmoregulatory Na+/myo-inositol cotransporter gene (SLC5A3): molecular cloning and localization to chromosome 21G T Berry, J J Mallee, H M Kwon, et al.
American Journal of Medical Genetics|April 23, 1999
Jagged1 mutations in patients ascertained with isolated congenital heart defectsI D Krantz, R Smith, R P Colliton, et al.
Pageof 7