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Journal of Medical Genetics
|
August 1, 1990
Linkage studies and deletion screening in choroideremia
A F Wright, R L Nussbaum, S S Bhattacharya, et al.
Genomics
|
April 1, 1990
DXS165 detects a translocation breakpoint in a woman with choroideremia and a de novo X; 13 translocation
D E Merry, J G Lesko, V Siu, et al.
American Journal of Human Genetics
|
September 1, 1984
Human chromosomal assignments for 14 argininosuccinate synthetase pseudogenes: cloned DNAs as reagents for cytogenetic analysis
T S Su, R L Nussbaum, S Airhart, et al.
American Journal of Human Genetics
|
June 1, 1997
Spectrum of mutations in the OCRL1 gene in the Lowe oculocerebrorenal syndrome
T Lin, B M Orrison, A M Leahey, et al.
Genomics
|
January 1, 1989
Physical fine mapping of the choroideremia locus using Xq21 deletions associated with complex syndromes
F P Cremers, D J van de Pol, P J Diergaarde, et al.
Molecular Psychiatry
|
December 19, 1998
Alpha synuclein is present in Lewy bodies in sporadic Parkinson's disease
E Mezey, A M Dehejia, G Harta, et al.
The Journal of Clinical Investigation
|
May 29, 1998
Functional overlap between murine Inpp5b and Ocrl1 may explain why deficiency of the murine ortholog for OCRL1 does not cause Lowe syndrome in mice
P A Jänne, S F Suchy, D Bernard, et al.
American Journal of Human Genetics
|
February 1, 1991
In situ hybridization to cytogenetic bands of yeast artificial chromosomes covering 50% of human Xq24-Xq28 DNA
V Montanaro, A Casamassimi, M D'Urso, et al.
Nature
|
July 16, 1992
The Lowe's oculocerebrorenal syndrome gene encodes a protein highly homologous to inositol polyphosphate-5-phosphatase
O Attree, I M Olivos, I Okabe, et al.
Genome Research
|
January 13, 2001
Human and mouse alpha-synuclein genes: comparative genomic sequence analysis and identification of a novel gene regulatory element
J W Touchman, A Dehejia, O Chiba-Falek, et al.
Page
of 12
Search research articles
Search
Showing results (91-100 of 115) with videos related to
Sort By:
Page
of 12
Journal of Medical Genetics
|
August 1, 1990
Linkage studies and deletion screening in choroideremia
A F Wright, R L Nussbaum, S S Bhattacharya, et al.
Genomics
|
April 1, 1990
DXS165 detects a translocation breakpoint in a woman with choroideremia and a de novo X; 13 translocation
D E Merry, J G Lesko, V Siu, et al.
American Journal of Human Genetics
|
September 1, 1984
Human chromosomal assignments for 14 argininosuccinate synthetase pseudogenes: cloned DNAs as reagents for cytogenetic analysis
T S Su, R L Nussbaum, S Airhart, et al.
American Journal of Human Genetics
|
June 1, 1997
Spectrum of mutations in the OCRL1 gene in the Lowe oculocerebrorenal syndrome
T Lin, B M Orrison, A M Leahey, et al.
Genomics
|
January 1, 1989
Physical fine mapping of the choroideremia locus using Xq21 deletions associated with complex syndromes
F P Cremers, D J van de Pol, P J Diergaarde, et al.
Molecular Psychiatry
|
December 19, 1998
Alpha synuclein is present in Lewy bodies in sporadic Parkinson's disease
E Mezey, A M Dehejia, G Harta, et al.
The Journal of Clinical Investigation
|
May 29, 1998
Functional overlap between murine Inpp5b and Ocrl1 may explain why deficiency of the murine ortholog for OCRL1 does not cause Lowe syndrome in mice
P A Jänne, S F Suchy, D Bernard, et al.
American Journal of Human Genetics
|
February 1, 1991
In situ hybridization to cytogenetic bands of yeast artificial chromosomes covering 50% of human Xq24-Xq28 DNA
V Montanaro, A Casamassimi, M D'Urso, et al.
Nature
|
July 16, 1992
The Lowe's oculocerebrorenal syndrome gene encodes a protein highly homologous to inositol polyphosphate-5-phosphatase
O Attree, I M Olivos, I Okabe, et al.
Genome Research
|
January 13, 2001
Human and mouse alpha-synuclein genes: comparative genomic sequence analysis and identification of a novel gene regulatory element
J W Touchman, A Dehejia, O Chiba-Falek, et al.
Page
of 12