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American Journal of Medical Genetics
|
December 23, 1999
Nonsyndromic congenital retinal nonattachment gene maps to human chromosome band 10q21
N M Ghiasvand, A B Kanis, C Helms, et al.
Human Molecular Genetics
|
August 1, 1993
A 2 base pair deletion in the RDS gene associated with butterfly-shaped pigment dystrophy of the fovea
B E Nichols, A V Drack, K Vandenburgh, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)
|
November 1, 1992
Ocular findings associated with rhodopsin gene codon 267 and codon 190 mutations in dominant retinitis pigmentosa
G A Fishman, K Vandenburgh, E M Stone, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)
|
June 1, 1994
Clinical features of a Stargardt-like dominant progressive macular dystrophy with genetic linkage to chromosome 6q
E M Stone, B E Nichols, A E Kimura, et al.
Gene
|
November 24, 1999
Evaluation and molecular characterization of EHD1, a candidate gene for Bardet-Biedl syndrome 1 (BBS1)
N B Haider, C Searby, E Galperin, et al.
Human Genetics
|
March 1, 1993
A denaturing gradient gel electrophoresis assay for sensitive detection of p53 mutations
J S Beck, A E Kwitek, P H Cogen, et al.
Human Molecular Genetics
|
January 1, 1995
Use of a DNA pooling strategy to identify a human obesity syndrome locus on chromosome 15
R Carmi, T Rokhlina, A E Kwitek-Black, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)
|
November 1, 1992
Procollagen II gene mutation in Stickler syndrome
D M Brown, B E Nichols, T A Weingeist, et al.
JAMA
|
June 22, 1999
Carrier rates in the midwestern United States for GJB2 mutations causing inherited deafness
G E Green, D A Scott, J M McDonald, et al.
The American Journal of Pathology
|
September 1, 1995
Microsatellite instability in adenocarcinoma of the prostate
R B Terrell, A H Wille, J C Cheville, et al.
Page
of 16
Search research articles
Search
Showing results (61-70 of 153) with videos related to
Sort By:
Page
of 16
American Journal of Medical Genetics
|
December 23, 1999
Nonsyndromic congenital retinal nonattachment gene maps to human chromosome band 10q21
N M Ghiasvand, A B Kanis, C Helms, et al.
Human Molecular Genetics
|
August 1, 1993
A 2 base pair deletion in the RDS gene associated with butterfly-shaped pigment dystrophy of the fovea
B E Nichols, A V Drack, K Vandenburgh, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)
|
November 1, 1992
Ocular findings associated with rhodopsin gene codon 267 and codon 190 mutations in dominant retinitis pigmentosa
G A Fishman, K Vandenburgh, E M Stone, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)
|
June 1, 1994
Clinical features of a Stargardt-like dominant progressive macular dystrophy with genetic linkage to chromosome 6q
E M Stone, B E Nichols, A E Kimura, et al.
Gene
|
November 24, 1999
Evaluation and molecular characterization of EHD1, a candidate gene for Bardet-Biedl syndrome 1 (BBS1)
N B Haider, C Searby, E Galperin, et al.
Human Genetics
|
March 1, 1993
A denaturing gradient gel electrophoresis assay for sensitive detection of p53 mutations
J S Beck, A E Kwitek, P H Cogen, et al.
Human Molecular Genetics
|
January 1, 1995
Use of a DNA pooling strategy to identify a human obesity syndrome locus on chromosome 15
R Carmi, T Rokhlina, A E Kwitek-Black, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)
|
November 1, 1992
Procollagen II gene mutation in Stickler syndrome
D M Brown, B E Nichols, T A Weingeist, et al.
JAMA
|
June 22, 1999
Carrier rates in the midwestern United States for GJB2 mutations causing inherited deafness
G E Green, D A Scott, J M McDonald, et al.
The American Journal of Pathology
|
September 1, 1995
Microsatellite instability in adenocarcinoma of the prostate
R B Terrell, A H Wille, J C Cheville, et al.
Page
of 16