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Biochemical Genetics
|
February 1, 1989
Organic aciduria and butyryl CoA dehydrogenase deficiency in BALB/cByJ mice
S P Schiffer, M Prochazka, P F Jezyk, et al.
Journal of the American College of Cardiology
|
August 1, 1985
Histologic studies on normal and persistent ductus arteriosus in the dog
A C Gittenberger-de Groot, J L Strengers, M Mentink, et al.
FEBS Letters
|
August 19, 1999
A missense mutation in canine C1C-1 causes recessive myotonia congenita in the dog
T H Rhodes, C H Vite, U Giger, et al.
Journal of the American Veterinary Medical Association
|
January 15, 1983
Defects in collagen fibrillogenesis causing hyperextensible, fragile skin in dogs
R R Minor, D H Lein, D F Patterson, et al.
Veterinary Pathology
|
July 3, 2004
Familial glomerulonephropathy in the Bullmastiff
M L Casal, D M Dambach, T Meister, et al.
Journal of the National Cancer Institute
|
February 1, 1978
Frequency of osteosarcoma among first-degree relatives of St. Bernard dogs
S Bech-Nielsen, M E Haskins, J S Reif, et al.
Human Genetics
|
December 29, 2000
Canine cystinuria: polymorphism in the canine SLC3A1 gene and identification of a nonsense mutation in cystinuric Newfoundland dogs
P S Henthorn, J Liu, T Gidalevich, et al.
Gene
|
February 12, 1996
A cDNA encoding canine muscle-type phosphofructokinase
B F Smith, P S Henthorn, Y Rajpurohit, et al.
The American Journal of Pathology
|
June 1, 1991
Mucopolysaccharidosis type VII (Sly syndrome). Beta-glucuronidase-deficient mucopolysaccharidosis in the dog
M E Haskins, G D Aguirre, P F Jezyk, et al.
Genomics
|
September 1, 1994
IL-2R gamma gene microdeletion demonstrates that canine X-linked severe combined immunodeficiency is a homologue of the human disease
P S Henthorn, R L Somberg, V M Fimiani, et al.
Page
of 12
Search research articles
Search
Showing results (81-90 of 118) with videos related to
Sort By:
Page
of 12
Biochemical Genetics
|
February 1, 1989
Organic aciduria and butyryl CoA dehydrogenase deficiency in BALB/cByJ mice
S P Schiffer, M Prochazka, P F Jezyk, et al.
Journal of the American College of Cardiology
|
August 1, 1985
Histologic studies on normal and persistent ductus arteriosus in the dog
A C Gittenberger-de Groot, J L Strengers, M Mentink, et al.
FEBS Letters
|
August 19, 1999
A missense mutation in canine C1C-1 causes recessive myotonia congenita in the dog
T H Rhodes, C H Vite, U Giger, et al.
Journal of the American Veterinary Medical Association
|
January 15, 1983
Defects in collagen fibrillogenesis causing hyperextensible, fragile skin in dogs
R R Minor, D H Lein, D F Patterson, et al.
Veterinary Pathology
|
July 3, 2004
Familial glomerulonephropathy in the Bullmastiff
M L Casal, D M Dambach, T Meister, et al.
Journal of the National Cancer Institute
|
February 1, 1978
Frequency of osteosarcoma among first-degree relatives of St. Bernard dogs
S Bech-Nielsen, M E Haskins, J S Reif, et al.
Human Genetics
|
December 29, 2000
Canine cystinuria: polymorphism in the canine SLC3A1 gene and identification of a nonsense mutation in cystinuric Newfoundland dogs
P S Henthorn, J Liu, T Gidalevich, et al.
Gene
|
February 12, 1996
A cDNA encoding canine muscle-type phosphofructokinase
B F Smith, P S Henthorn, Y Rajpurohit, et al.
The American Journal of Pathology
|
June 1, 1991
Mucopolysaccharidosis type VII (Sly syndrome). Beta-glucuronidase-deficient mucopolysaccharidosis in the dog
M E Haskins, G D Aguirre, P F Jezyk, et al.
Genomics
|
September 1, 1994
IL-2R gamma gene microdeletion demonstrates that canine X-linked severe combined immunodeficiency is a homologue of the human disease
P S Henthorn, R L Somberg, V M Fimiani, et al.
Page
of 12