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Human Molecular Genetics
|
April 1, 1996
Phenotypic variation in Waardenburg syndrome: mutational heterogeneity, modifier genes or polygenic background?
A Pandya, X J Xia, B L Landa, et al.
Nature Genetics
|
July 3, 1999
Mutations in a novel retina-specific gene cause autosomal dominant retinitis pigmentosa
L S Sullivan, J R Heckenlively, S J Bowne, et al.
American Journal of Medical Genetics
|
March 8, 2000
Manifestations and linkage analysis in X-linked autoimmunity-immunodeficiency syndrome
P J Ferguson, S H Blanton, F T Saulsbury, et al.
American Journal of Medical Genetics. Part A
|
June 9, 2012
Studies of TBX4 and chromosome 17q23.1q23.2: an uncommon cause of nonsyndromic clubfoot
W Lu, C A Bacino, B S Richards, et al.
American Journal of Medical Genetics. Part A
|
November 12, 2005
Promotor genotype of the platelet-derived growth factor receptor-alpha gene shows population stratification but not association with spina bifida meningomyelocele
K-S Au, H Northrup, T J Kirkpatrick, et al.
Human Molecular Genetics
|
May 1, 1994
Localization of the achondroplasia gene to the distal 2.5 Mb of human chromosome 4p
C A Francomano, R I Ortiz de Luna, T W Hefferon, et al.
Clinical Genetics
|
September 5, 2001
Haplotype analysis of the USH1D locus and genotype-phenotype correlations
X Z Liu, S H Blanton, M Bitner-Glindzicz, et al.
Clinical Genetics
|
September 9, 2015
A Mayan founder mutation is a common cause of deafness in Guatemala
C Carranza, I Menendez, M Herrera, et al.
Journal of Human Hypertension
|
June 3, 2016
Utility of blood pressure genetic risk score in admixed Hispanic samples
A H Beecham, L Wang, N Vasudeva, et al.
Human Heredity
|
May 9, 2000
Fine mapping of the human biotinidase gene and haplotype analysis of five common mutations
S H Blanton, A Pandya, B L Landa, et al.
Page
of 6
Search research articles
Search
Showing results (41-50 of 53) with videos related to
Sort By:
Page
of 6
Human Molecular Genetics
|
April 1, 1996
Phenotypic variation in Waardenburg syndrome: mutational heterogeneity, modifier genes or polygenic background?
A Pandya, X J Xia, B L Landa, et al.
Nature Genetics
|
July 3, 1999
Mutations in a novel retina-specific gene cause autosomal dominant retinitis pigmentosa
L S Sullivan, J R Heckenlively, S J Bowne, et al.
American Journal of Medical Genetics
|
March 8, 2000
Manifestations and linkage analysis in X-linked autoimmunity-immunodeficiency syndrome
P J Ferguson, S H Blanton, F T Saulsbury, et al.
American Journal of Medical Genetics. Part A
|
June 9, 2012
Studies of TBX4 and chromosome 17q23.1q23.2: an uncommon cause of nonsyndromic clubfoot
W Lu, C A Bacino, B S Richards, et al.
American Journal of Medical Genetics. Part A
|
November 12, 2005
Promotor genotype of the platelet-derived growth factor receptor-alpha gene shows population stratification but not association with spina bifida meningomyelocele
K-S Au, H Northrup, T J Kirkpatrick, et al.
Human Molecular Genetics
|
May 1, 1994
Localization of the achondroplasia gene to the distal 2.5 Mb of human chromosome 4p
C A Francomano, R I Ortiz de Luna, T W Hefferon, et al.
Clinical Genetics
|
September 5, 2001
Haplotype analysis of the USH1D locus and genotype-phenotype correlations
X Z Liu, S H Blanton, M Bitner-Glindzicz, et al.
Clinical Genetics
|
September 9, 2015
A Mayan founder mutation is a common cause of deafness in Guatemala
C Carranza, I Menendez, M Herrera, et al.
Journal of Human Hypertension
|
June 3, 2016
Utility of blood pressure genetic risk score in admixed Hispanic samples
A H Beecham, L Wang, N Vasudeva, et al.
Human Heredity
|
May 9, 2000
Fine mapping of the human biotinidase gene and haplotype analysis of five common mutations
S H Blanton, A Pandya, B L Landa, et al.
Page
of 6