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S Jeffery

Showing results (161-170 of 181) with videos related to

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Human Genetics|May 8, 2000
Linkage of recessive Robinow syndrome to a 4 cM interval on chromosome 9q22A R Afzal, A Rajab, C Fenske, et al.
Genetic Testing|August 16, 2002
T594M mutation of the beta-subunit of the epithelial sodium channel in Ghanaian populations from Kumasi and London and a possible association with hypertensionY B Dong, J Plange-Rhule, I Owusu, et al.
Nature Genetics|December 1, 1994
Mapping a gene for Noonan syndrome to the long arm of chromosome 12C R Jamieson, I van der Burgt, A F Brady, et al.
American Journal of Medical Genetics|July 27, 2001
Silver syndrome is not linked to any of the previously established autosomal dominant hereditary spastic paraplegia lociH Patel, P E Hart, T Warner, et al.
The Journal of Infectious Diseases|March 1, 1989
Phaeohyphomycotic cutaneous disease caused by Pleurophoma in a cardiac transplant patientD P Dooley, M L Beckius, B S Jeffery, et al.
Journal of Medical Genetics|July 13, 2002
Analysis of the phenotypic abnormalities in lymphoedema-distichiasis syndrome in 74 patients with FOXC2 mutations or linkage to 16q24G Brice, S Mansour, R Bell, et al.
Nature Genetics|August 10, 2000
Recessive Robinow syndrome, allelic to dominant brachydactyly type B, is caused by mutation of ROR2A R Afzal, A Rajab, C D Fenske, et al.
Clinical Science (London, England : 1979)|December 1, 1998
Transforming growth factor-beta1 gene polymorphisms and coronary artery diseaseP Syrris, N D Carter, J C Metcalfe, et al.
Circulation|February 23, 1999
Interleukin-1 receptor antagonist gene polymorphism and coronary artery diseaseS E Francis, N J Camp, R M Dewberry, et al.
Human Genetics|August 14, 2001
Analysis of lymphoedema-distichiasis families for FOXC2 mutations reveals small insertions and deletions throughout the geneR Bell, G Brice, A H Child, et al.
Pageof 19

Showing results (161-170 of 181) with videos related to

Sort By:
Pageof 19
Human Genetics|May 8, 2000
Linkage of recessive Robinow syndrome to a 4 cM interval on chromosome 9q22A R Afzal, A Rajab, C Fenske, et al.
Genetic Testing|August 16, 2002
T594M mutation of the beta-subunit of the epithelial sodium channel in Ghanaian populations from Kumasi and London and a possible association with hypertensionY B Dong, J Plange-Rhule, I Owusu, et al.
Nature Genetics|December 1, 1994
Mapping a gene for Noonan syndrome to the long arm of chromosome 12C R Jamieson, I van der Burgt, A F Brady, et al.
American Journal of Medical Genetics|July 27, 2001
Silver syndrome is not linked to any of the previously established autosomal dominant hereditary spastic paraplegia lociH Patel, P E Hart, T Warner, et al.
The Journal of Infectious Diseases|March 1, 1989
Phaeohyphomycotic cutaneous disease caused by Pleurophoma in a cardiac transplant patientD P Dooley, M L Beckius, B S Jeffery, et al.
Journal of Medical Genetics|July 13, 2002
Analysis of the phenotypic abnormalities in lymphoedema-distichiasis syndrome in 74 patients with FOXC2 mutations or linkage to 16q24G Brice, S Mansour, R Bell, et al.
Nature Genetics|August 10, 2000
Recessive Robinow syndrome, allelic to dominant brachydactyly type B, is caused by mutation of ROR2A R Afzal, A Rajab, C D Fenske, et al.
Clinical Science (London, England : 1979)|December 1, 1998
Transforming growth factor-beta1 gene polymorphisms and coronary artery diseaseP Syrris, N D Carter, J C Metcalfe, et al.
Circulation|February 23, 1999
Interleukin-1 receptor antagonist gene polymorphism and coronary artery diseaseS E Francis, N J Camp, R M Dewberry, et al.
Human Genetics|August 14, 2001
Analysis of lymphoedema-distichiasis families for FOXC2 mutations reveals small insertions and deletions throughout the geneR Bell, G Brice, A H Child, et al.
Pageof 19