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American Journal of Human Genetics
|
April 1, 1992
Recurrent 3-bp deletion at codon 255/256 of the rhodopsin gene in a German pedigree with autosomal dominant retinitis pigmentosa
A Artlich, M Horn, B Lorenz, et al.
Journal of Inherited Metabolic Disease
|
October 23, 2008
Association between polymorphisms of endothelial nitric oxide synthase gene (NOS3) and left posterior wall thickness (LPWT) of the heart in Fabry disease
I Rohard, E Schaefer, C Kampmann, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)
|
March 1, 1996
Variable expressivity in a Japanese family with autosomal dominant retinitis pigmentosa closely linked to chromosome 19q
M Nakazawa, S Xu, A Gal, et al.
Retina (Philadelphia, Pa.)
|
January 1, 1997
Oguchi disease: phenotypic characteristics of patients with the frequent 1147delA mutation in the arrestin gene
M Nakazawa, Y Wada, S Fuchs, et al.
Journal of Oral & Facial Pain and Headache
|
June 28, 2019
Simultaneous Noxious Stimulation of the Human Anterior Temporalis and Masseter Muscles. Part I: Effects on Jaw Movements
Magda Amhamed, Terry Whittle, John A Gal, et al.
American Journal of Medical Genetics
|
August 22, 1997
Molecular analysis of the L1CAM gene in patients with X-linked hydrocephalus demonstrates eight novel mutations and suggests non-allelic heterogeneity of the trait
S M Gu, U Orth, M Zankl, et al.
International Journal of Legal Medicine
|
March 31, 2000
Sudden death due to cerebrotendinous xanthomatosis confirmed by mutation analysis
J P Sperhake, J Matschke, U Orth, et al.
Medicine and Science in Sports and Exercise
|
December 1, 1995
Left ventricular ejection fraction during incremental and steady state exercise
C Foster, R A Gal, S C Port, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
August 1, 1984
Differential DNase I sensitivity of the albumin and alpha-fetoprotein genes in chromatin from rat tissues and cell lines
J L Nahon, A Gal, T Erdos, et al.
Ophthalmic Genetics
|
June 1, 1996
Ocular phenotypes associated with two mutations (R121W, C126X) in the Norrie disease gene
U Kellner, S Fuchs, N Bornfeld, et al.
Page
of 49
Search research articles
Search
Showing results (151-160 of 488) with videos related to
Sort By:
Page
of 49
American Journal of Human Genetics
|
April 1, 1992
Recurrent 3-bp deletion at codon 255/256 of the rhodopsin gene in a German pedigree with autosomal dominant retinitis pigmentosa
A Artlich, M Horn, B Lorenz, et al.
Journal of Inherited Metabolic Disease
|
October 23, 2008
Association between polymorphisms of endothelial nitric oxide synthase gene (NOS3) and left posterior wall thickness (LPWT) of the heart in Fabry disease
I Rohard, E Schaefer, C Kampmann, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)
|
March 1, 1996
Variable expressivity in a Japanese family with autosomal dominant retinitis pigmentosa closely linked to chromosome 19q
M Nakazawa, S Xu, A Gal, et al.
Retina (Philadelphia, Pa.)
|
January 1, 1997
Oguchi disease: phenotypic characteristics of patients with the frequent 1147delA mutation in the arrestin gene
M Nakazawa, Y Wada, S Fuchs, et al.
Journal of Oral & Facial Pain and Headache
|
June 28, 2019
Simultaneous Noxious Stimulation of the Human Anterior Temporalis and Masseter Muscles. Part I: Effects on Jaw Movements
Magda Amhamed, Terry Whittle, John A Gal, et al.
American Journal of Medical Genetics
|
August 22, 1997
Molecular analysis of the L1CAM gene in patients with X-linked hydrocephalus demonstrates eight novel mutations and suggests non-allelic heterogeneity of the trait
S M Gu, U Orth, M Zankl, et al.
International Journal of Legal Medicine
|
March 31, 2000
Sudden death due to cerebrotendinous xanthomatosis confirmed by mutation analysis
J P Sperhake, J Matschke, U Orth, et al.
Medicine and Science in Sports and Exercise
|
December 1, 1995
Left ventricular ejection fraction during incremental and steady state exercise
C Foster, R A Gal, S C Port, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
August 1, 1984
Differential DNase I sensitivity of the albumin and alpha-fetoprotein genes in chromatin from rat tissues and cell lines
J L Nahon, A Gal, T Erdos, et al.
Ophthalmic Genetics
|
June 1, 1996
Ocular phenotypes associated with two mutations (R121W, C126X) in the Norrie disease gene
U Kellner, S Fuchs, N Bornfeld, et al.
Page
of 49