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P R Fain

Showing results (41-50 of 53) with videos related to

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Nature Genetics|March 1, 1995
A 2D crossover-based map of the human X chromosome as a model for map integrationP R Fain, E N Kort, P F Chance, et al.
Oncogene|November 1, 1994
A germline 2.35 kb deletion of p53 genomic DNA creating a specific loss of the oligomerization domain inherited in a Li-Fraumeni syndrome familyS J Plummer, M Santibáñez-Koref, T Kurosaki, et al.
Journal of Medical Genetics|March 1, 1992
Clinical variability of type 1 neurofibromatosis: is there a neurofibromatosis-Noonan syndrome?H J Stern, H M Saal, J S Lee, et al.
American Journal of Human Genetics|June 1, 1996
A mutation causing Alport syndrome with tardive hearing loss is common in the western United StatesD F Barker, C J Pruchno, X Jiang, et al.
Genomics|December 1, 1987
Genetic analysis of NF1: identification of close flanking markers on chromosome 17P R Fain, D F Barker, D E Goldgar, et al.
Genetic Epidemiology|January 1, 1996
BRCA1 R841W: a strong candidate for a common mutation with moderate phenotypeD F Barker, E R Almeida, G Casey, et al.
The Journal of Clinical Investigation|October 28, 1998
Evidence for oligogenic inheritance of type 1 diabetes in a large Bedouin Arab familyC F Verge, P Vardi, S Babu, et al.
Genes and Immunity|August 31, 2007
Differential effects of DRB1*0301 and DQA1*0501-DQB1*0201 on the activation and progression of islet cell autoimmunityE Eller, P Vardi, K K McFann, et al.
The Journal of Clinical Endocrinology and Metabolism|November 1, 1994
Fine structure mapping of the human X-linked hypophosphatemic rickets gene locusM J Econs, P S Rowe, F Francis, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|September 1, 1993
Flanking markers define the X-linked hypophosphatemic rickets gene locusM J Econs, P R Fain, M Norman, et al.
Pageof 6

Showing results (41-50 of 53) with videos related to

Sort By:
Pageof 6
Nature Genetics|March 1, 1995
A 2D crossover-based map of the human X chromosome as a model for map integrationP R Fain, E N Kort, P F Chance, et al.
Oncogene|November 1, 1994
A germline 2.35 kb deletion of p53 genomic DNA creating a specific loss of the oligomerization domain inherited in a Li-Fraumeni syndrome familyS J Plummer, M Santibáñez-Koref, T Kurosaki, et al.
Journal of Medical Genetics|March 1, 1992
Clinical variability of type 1 neurofibromatosis: is there a neurofibromatosis-Noonan syndrome?H J Stern, H M Saal, J S Lee, et al.
American Journal of Human Genetics|June 1, 1996
A mutation causing Alport syndrome with tardive hearing loss is common in the western United StatesD F Barker, C J Pruchno, X Jiang, et al.
Genomics|December 1, 1987
Genetic analysis of NF1: identification of close flanking markers on chromosome 17P R Fain, D F Barker, D E Goldgar, et al.
Genetic Epidemiology|January 1, 1996
BRCA1 R841W: a strong candidate for a common mutation with moderate phenotypeD F Barker, E R Almeida, G Casey, et al.
The Journal of Clinical Investigation|October 28, 1998
Evidence for oligogenic inheritance of type 1 diabetes in a large Bedouin Arab familyC F Verge, P Vardi, S Babu, et al.
Genes and Immunity|August 31, 2007
Differential effects of DRB1*0301 and DQA1*0501-DQB1*0201 on the activation and progression of islet cell autoimmunityE Eller, P Vardi, K K McFann, et al.
The Journal of Clinical Endocrinology and Metabolism|November 1, 1994
Fine structure mapping of the human X-linked hypophosphatemic rickets gene locusM J Econs, P S Rowe, F Francis, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|September 1, 1993
Flanking markers define the X-linked hypophosphatemic rickets gene locusM J Econs, P R Fain, M Norman, et al.
Pageof 6