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Gastroenterology
|
July 1, 1987
Diffuse hepatocellular dysplasia and carcinoma associated with the Mmalton variant of alpha 1-antitrypsin
C L Reid, G J Wiener, D W Cox, et al.
Nature Genetics
|
February 1, 1995
The Wilson disease gene: spectrum of mutations and their consequences
G R Thomas, J R Forbes, E A Roberts, et al.
Sexually Transmitted Diseases
|
October 1, 1983
A preliminary evaluation of the Gonozyme test
M Burns, P H Rossi, D W Cox, et al.
Human Genetics
|
December 1, 1994
The immunoglobulin heavy chain and disease association: application to pemphigus vulgaris
W T Gibson, M A Walter, A R Ahmed, et al.
Brain Research
|
July 14, 1980
Release of amino acids from chronic epileptic and subepileptic foci in vivo
P R Dodd, H F Bradford, A S Abdul-Ghani, et al.
Lancet (London, England)
|
October 4, 1986
Prenatal diagnosis of alpha 1-antitrypsin deficiency by restriction fragment length polymorphisms, and comparison with oligonucleotide probe analysis
J F Hejtmancik, R N Sifers, P A Ward, et al.
European Journal of Gastroenterology & Hepatology
|
May 8, 2001
Genotype-phenotype interactions in Wilson's disease: insight from an Icelandic mutation
R Palsson, J G Jonasson, M Kristjansson, et al.
European Journal of Human Genetics : EJHG
|
January 1, 1996
Maternal uniparental isodisomy of human chromosome 14 associated with a paternal t(13q14q) and precocious puberty
D J Tomkins, A F Roux, J Waye, et al.
Genomics
|
April 1, 1991
Localization and genetic linkage of the human immunoglobulin heavy chain genes and the creatine kinase brain (CKB) gene: identification of a hot spot for recombination
J C Benger, I Teshima, M A Walter, et al.
Respiratory Research
|
December 19, 2018
Pulmonary aspiration in preschool children with cystic fibrosis
D Clarke, I Gorman, F Ringholz, et al.
Page
of 23
Search research articles
Search
Showing results (181-190 of 223) with videos related to
Sort By:
Page
of 23
Gastroenterology
|
July 1, 1987
Diffuse hepatocellular dysplasia and carcinoma associated with the Mmalton variant of alpha 1-antitrypsin
C L Reid, G J Wiener, D W Cox, et al.
Nature Genetics
|
February 1, 1995
The Wilson disease gene: spectrum of mutations and their consequences
G R Thomas, J R Forbes, E A Roberts, et al.
Sexually Transmitted Diseases
|
October 1, 1983
A preliminary evaluation of the Gonozyme test
M Burns, P H Rossi, D W Cox, et al.
Human Genetics
|
December 1, 1994
The immunoglobulin heavy chain and disease association: application to pemphigus vulgaris
W T Gibson, M A Walter, A R Ahmed, et al.
Brain Research
|
July 14, 1980
Release of amino acids from chronic epileptic and subepileptic foci in vivo
P R Dodd, H F Bradford, A S Abdul-Ghani, et al.
Lancet (London, England)
|
October 4, 1986
Prenatal diagnosis of alpha 1-antitrypsin deficiency by restriction fragment length polymorphisms, and comparison with oligonucleotide probe analysis
J F Hejtmancik, R N Sifers, P A Ward, et al.
European Journal of Gastroenterology & Hepatology
|
May 8, 2001
Genotype-phenotype interactions in Wilson's disease: insight from an Icelandic mutation
R Palsson, J G Jonasson, M Kristjansson, et al.
European Journal of Human Genetics : EJHG
|
January 1, 1996
Maternal uniparental isodisomy of human chromosome 14 associated with a paternal t(13q14q) and precocious puberty
D J Tomkins, A F Roux, J Waye, et al.
Genomics
|
April 1, 1991
Localization and genetic linkage of the human immunoglobulin heavy chain genes and the creatine kinase brain (CKB) gene: identification of a hot spot for recombination
J C Benger, I Teshima, M A Walter, et al.
Respiratory Research
|
December 19, 2018
Pulmonary aspiration in preschool children with cystic fibrosis
D Clarke, I Gorman, F Ringholz, et al.
Page
of 23