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American Journal of Human Genetics
|
October 1, 1986
The X chromosome shows less genetic variation at restriction sites than the autosomes
M H Hofker, M I Skraastad, A A Bergen, et al.
Genomics
|
December 1, 1991
Generation and fluorescent in situ hybridization mapping of yeast artificial chromosomes of 1p, 17p, 17q, and 19q from a hybrid cell line by high-density screening of an amplified library
M S Driesen, J G Dauwerse, M C Wapenaar, et al.
Genomics
|
September 2, 1998
Characterization of Cxorf5 (71-7A), a novel human cDNA mapping to Xp22 and encoding a protein containing coiled-coil alpha-helical domains
L de Conciliis, A Marchitiello, M C Wapenaar, et al.
Genomics
|
May 1, 1992
Physical mapping of 14 new DNA markers isolated from the human distal Xp region
M C Wapenaar, C Petit, E Basler, et al.
Genomics
|
February 1, 1988
A deletion hot spot in the Duchenne muscular dystrophy gene
M C Wapenaar, T Kievits, K A Hart, et al.
Cytogenetics and Cell Genetics
|
January 1, 1993
Detection of a new submicroscopic Norrie disease deletion interval with a novel DNA probe isolated by differential Alu PCR fingerprint cloning
A A Bergen, M C Wapenaar, E J Schuurman, et al.
Nucleic Acids Research
|
July 25, 1989
High resolution deletion breakpoint mapping in the DMD gene by whole cosmid hybridization
L A Blonden, J T den Dunnen, H M van Paassen, et al.
Nature Genetics
|
July 1, 1993
A high resolution deletion map of human chromosome Xp22
L Schaefer, G B Ferrero, A Grillo, et al.
Human Molecular Genetics
|
April 1, 1994
A gene from the Xp22.3 region shares homology with voltage-gated chloride channels
M A van Slegtenhorst, M T Bassi, G Borsani, et al.
Neurology
|
January 1, 1988
Duchenne muscular dystrophy: high frequency of deletions
R J Bartlett, M A Pericak-Vance, J Koh, et al.
Page
of 3
Search research articles
Search
Showing results (11-20 of 23) with videos related to
Sort By:
Page
of 3
American Journal of Human Genetics
|
October 1, 1986
The X chromosome shows less genetic variation at restriction sites than the autosomes
M H Hofker, M I Skraastad, A A Bergen, et al.
Genomics
|
December 1, 1991
Generation and fluorescent in situ hybridization mapping of yeast artificial chromosomes of 1p, 17p, 17q, and 19q from a hybrid cell line by high-density screening of an amplified library
M S Driesen, J G Dauwerse, M C Wapenaar, et al.
Genomics
|
September 2, 1998
Characterization of Cxorf5 (71-7A), a novel human cDNA mapping to Xp22 and encoding a protein containing coiled-coil alpha-helical domains
L de Conciliis, A Marchitiello, M C Wapenaar, et al.
Genomics
|
May 1, 1992
Physical mapping of 14 new DNA markers isolated from the human distal Xp region
M C Wapenaar, C Petit, E Basler, et al.
Genomics
|
February 1, 1988
A deletion hot spot in the Duchenne muscular dystrophy gene
M C Wapenaar, T Kievits, K A Hart, et al.
Cytogenetics and Cell Genetics
|
January 1, 1993
Detection of a new submicroscopic Norrie disease deletion interval with a novel DNA probe isolated by differential Alu PCR fingerprint cloning
A A Bergen, M C Wapenaar, E J Schuurman, et al.
Nucleic Acids Research
|
July 25, 1989
High resolution deletion breakpoint mapping in the DMD gene by whole cosmid hybridization
L A Blonden, J T den Dunnen, H M van Paassen, et al.
Nature Genetics
|
July 1, 1993
A high resolution deletion map of human chromosome Xp22
L Schaefer, G B Ferrero, A Grillo, et al.
Human Molecular Genetics
|
April 1, 1994
A gene from the Xp22.3 region shares homology with voltage-gated chloride channels
M A van Slegtenhorst, M T Bassi, G Borsani, et al.
Neurology
|
January 1, 1988
Duchenne muscular dystrophy: high frequency of deletions
R J Bartlett, M A Pericak-Vance, J Koh, et al.
Page
of 3