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Human Heredity
|
January 1, 1983
HLA haplotype segregation in families of type 1 diabetics
L J Walsh, R M Ehrlich, J A Falk, et al.
Nucleic Acids Research
|
May 27, 1986
Three RFLPs recognized by an anonymous sequence localized to 21q11.2 [HGM8 D21S72]
P J Goodfellow, A M Duncan, N E Simpson, et al.
Canadian Medical Association Journal
|
September 9, 1978
Hereditary angioneurotic edema and Charcot-Marie-Tooth disease in the same family
P G Fernandez, J H Day, N E Simpson, et al.
Canadian Medical Association Journal
|
February 15, 1981
Multiple endocrine neoplasia, type II: a combined surgical and genetic approach to treatment
M W Partington, W R Ghent, E V Sears, et al.
Acta Oto-Laryngologica
|
May 1, 1979
Binocular counterrolling in humans during dynamic rotation
S G Diamond, C H Markham, N E Simpson, et al.
Human Genetics
|
December 18, 1978
Confirmation of regional assignment of nucleoside phosphorylase (NP) on chromosome 14 by gene dosage studies
M Frecker, L Dallaire, S R Young, et al.
Journal of Materials Science. Materials in Medicine
|
June 2, 2005
Effects of alginate encapsulation on mitochondrial activity
J Oca-Cossio, N E Simpson, Z Han, et al.
Biochemical and Biophysical Research Communications
|
July 13, 2000
Effects of pH on murine insulinoma betaTC3 cells
N E Simpson, L K Bennett, K K Papas, et al.
American Journal of Medical Genetics
|
January 1, 1981
Familial cutaneous amyloidosis with systemic manifestations in males
M W Partington, P J Marriott, R S Prentice, et al.
Journal of Neurogenetics
|
July 1, 1986
Localization of X-linked dominant Charcot-Marie-Tooth disease (CMT 2) to Xq13
J Beckett, J J Holden, N E Simpson, et al.
Page
of 10
Search research articles
Search
Showing results (51-60 of 91) with videos related to
Sort By:
Page
of 10
Human Heredity
|
January 1, 1983
HLA haplotype segregation in families of type 1 diabetics
L J Walsh, R M Ehrlich, J A Falk, et al.
Nucleic Acids Research
|
May 27, 1986
Three RFLPs recognized by an anonymous sequence localized to 21q11.2 [HGM8 D21S72]
P J Goodfellow, A M Duncan, N E Simpson, et al.
Canadian Medical Association Journal
|
September 9, 1978
Hereditary angioneurotic edema and Charcot-Marie-Tooth disease in the same family
P G Fernandez, J H Day, N E Simpson, et al.
Canadian Medical Association Journal
|
February 15, 1981
Multiple endocrine neoplasia, type II: a combined surgical and genetic approach to treatment
M W Partington, W R Ghent, E V Sears, et al.
Acta Oto-Laryngologica
|
May 1, 1979
Binocular counterrolling in humans during dynamic rotation
S G Diamond, C H Markham, N E Simpson, et al.
Human Genetics
|
December 18, 1978
Confirmation of regional assignment of nucleoside phosphorylase (NP) on chromosome 14 by gene dosage studies
M Frecker, L Dallaire, S R Young, et al.
Journal of Materials Science. Materials in Medicine
|
June 2, 2005
Effects of alginate encapsulation on mitochondrial activity
J Oca-Cossio, N E Simpson, Z Han, et al.
Biochemical and Biophysical Research Communications
|
July 13, 2000
Effects of pH on murine insulinoma betaTC3 cells
N E Simpson, L K Bennett, K K Papas, et al.
American Journal of Medical Genetics
|
January 1, 1981
Familial cutaneous amyloidosis with systemic manifestations in males
M W Partington, P J Marriott, R S Prentice, et al.
Journal of Neurogenetics
|
July 1, 1986
Localization of X-linked dominant Charcot-Marie-Tooth disease (CMT 2) to Xq13
J Beckett, J J Holden, N E Simpson, et al.
Page
of 10