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Journal of Medical Genetics
|
November 1, 1995
Evaluation of candidate genes for familial brachydactyly
J M Mastrobattista, P Dollé, S H Blanton, et al.
American Journal of Medical Genetics
|
August 1, 1994
XLPRA: a canine retinal degeneration inherited as an X-linked trait
G M Acland, S H Blanton, B Hershfield, et al.
Genomics
|
January 1, 1993
Linkage studies of the esterase D and retinoblastoma genes to canine copper toxicosis: a model for Wilson disease
V Yuzbasiyan-Gurkan, S Wagnitz, S H Blanton, et al.
Journal of Medical Genetics
|
July 1, 1996
Report of a critical recombination further narrowing the TSC1 region
K S Au, J Murrell, A Buckler, et al.
Clinical Genetics
|
September 10, 2004
Genetic analysis of primary microcephaly in Indian families: novel ASPM mutations
A Kumar, S H Blanton, M Babu, et al.
Chinese Medical Journal
|
June 1, 1992
Linkage between Rh blood group and autosomal dominant retinitis pigmentosa in ten Chinese families
Y J Fei, S H Blanton, S P Daiger, et al.
American Journal of Human Genetics
|
June 1, 1993
Nonsyndromic cleft lip and palate: no evidence of linkage to HLA or factor 13A
J T Hecht, Y Wang, B Connor, et al.
Investigative Ophthalmology & Visual Science
|
December 1, 1994
Cosegregation of codon 807 mutation of the canine rod cGMP phosphodiesterase beta gene and rcd1
K Ray, V J Baldwin, G M Acland, et al.
American Journal of Medical Genetics
|
March 15, 1996
Hereditary multiple exostoses: confirmation of linkage to chromosomes 8 and 11
S H Blanton, D Hogue, M Wagner, et al.
Journal of Orthopaedic Research : Official Publication of the Orthopaedic Research Society
|
November 1, 1996
Genetic analysis of structural elastic fiber and collagen genes in familial adolescent idiopathic scoliosis
N H Miller, B Mims, A Child, et al.
Page
of 6
Search research articles
Search
Showing results (1-10 of 53) with videos related to
Sort By:
Page
of 6
Journal of Medical Genetics
|
November 1, 1995
Evaluation of candidate genes for familial brachydactyly
J M Mastrobattista, P Dollé, S H Blanton, et al.
American Journal of Medical Genetics
|
August 1, 1994
XLPRA: a canine retinal degeneration inherited as an X-linked trait
G M Acland, S H Blanton, B Hershfield, et al.
Genomics
|
January 1, 1993
Linkage studies of the esterase D and retinoblastoma genes to canine copper toxicosis: a model for Wilson disease
V Yuzbasiyan-Gurkan, S Wagnitz, S H Blanton, et al.
Journal of Medical Genetics
|
July 1, 1996
Report of a critical recombination further narrowing the TSC1 region
K S Au, J Murrell, A Buckler, et al.
Clinical Genetics
|
September 10, 2004
Genetic analysis of primary microcephaly in Indian families: novel ASPM mutations
A Kumar, S H Blanton, M Babu, et al.
Chinese Medical Journal
|
June 1, 1992
Linkage between Rh blood group and autosomal dominant retinitis pigmentosa in ten Chinese families
Y J Fei, S H Blanton, S P Daiger, et al.
American Journal of Human Genetics
|
June 1, 1993
Nonsyndromic cleft lip and palate: no evidence of linkage to HLA or factor 13A
J T Hecht, Y Wang, B Connor, et al.
Investigative Ophthalmology & Visual Science
|
December 1, 1994
Cosegregation of codon 807 mutation of the canine rod cGMP phosphodiesterase beta gene and rcd1
K Ray, V J Baldwin, G M Acland, et al.
American Journal of Medical Genetics
|
March 15, 1996
Hereditary multiple exostoses: confirmation of linkage to chromosomes 8 and 11
S H Blanton, D Hogue, M Wagner, et al.
Journal of Orthopaedic Research : Official Publication of the Orthopaedic Research Society
|
November 1, 1996
Genetic analysis of structural elastic fiber and collagen genes in familial adolescent idiopathic scoliosis
N H Miller, B Mims, A Child, et al.
Page
of 6