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Journal of Medical Genetics
|
December 19, 2001
Mutation analysis of TBX1 in non-deleted patients with features of DGS/VCFS or isolated cardiovascular defects
W Gong, S Gottlieb, J Collins, et al.
Genome Research
|
January 1, 1997
A region of mouse chromosome 16 is syntenic to the DiGeorge, velocardiofacial syndrome minimal critical region
N Galili, H S Baldwin, J Lund, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
May 30, 1998
t(11;22)(q23;q11.2) In acute myeloid leukemia of infant twins fuses MLL with hCDCrel, a cell division cycle gene in the genomic region of deletion in DiGeorge and velocardiofacial syndromes
M D Megonigal, E F Rappaport, D H Jones, et al.
American Journal of Medical Genetics
|
September 15, 1992
Deletions and microdeletions of 22q11.2 in velo-cardio-facial syndrome
D A Driscoll, N B Spinner, M L Budarf, et al.
Journal of Medical Genetics
|
October 3, 1999
Microdeletion 22q11.2: clinical data and deletion size
W S Kerstjens-Frederikse, H Kurahashi, D A Driscoll, et al.
Human Molecular Genetics
|
March 4, 2000
Chromosome 22-specific low copy repeats and the 22q11.2 deletion syndrome: genomic organization and deletion endpoint analysis
T H Shaikh, H Kurahashi, S C Saitta, et al.
Human Molecular Genetics
|
March 1, 1997
Disruption of the clathrin heavy chain-like gene (CLTCL) associated with features of DGS/VCFS: a balanced (21;22)(p12;q11) translocation
S E Holmes, M A Riazi, W Gong, et al.
Genomics
|
July 15, 1996
Regional localization of over 300 loci on human chromosome 22 using a somatic cell hybrid mapping panel
M L Budarf, B Eckman, D Michaud, et al.
Genes and Immunity
|
October 22, 2010
A targeted association study in systemic lupus erythematosus identifies multiple susceptibility alleles
M L Budarf, P Goyette, G Boucher, et al.
Page
of 6
Search research articles
Search
Showing results (51-60 of 59) with videos related to
Sort By:
Page
of 6
You have reached the last page of results.
This site can display upto 59 results.
Journal of Medical Genetics
|
December 19, 2001
Mutation analysis of TBX1 in non-deleted patients with features of DGS/VCFS or isolated cardiovascular defects
W Gong, S Gottlieb, J Collins, et al.
Genome Research
|
January 1, 1997
A region of mouse chromosome 16 is syntenic to the DiGeorge, velocardiofacial syndrome minimal critical region
N Galili, H S Baldwin, J Lund, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
May 30, 1998
t(11;22)(q23;q11.2) In acute myeloid leukemia of infant twins fuses MLL with hCDCrel, a cell division cycle gene in the genomic region of deletion in DiGeorge and velocardiofacial syndromes
M D Megonigal, E F Rappaport, D H Jones, et al.
American Journal of Medical Genetics
|
September 15, 1992
Deletions and microdeletions of 22q11.2 in velo-cardio-facial syndrome
D A Driscoll, N B Spinner, M L Budarf, et al.
Journal of Medical Genetics
|
October 3, 1999
Microdeletion 22q11.2: clinical data and deletion size
W S Kerstjens-Frederikse, H Kurahashi, D A Driscoll, et al.
Human Molecular Genetics
|
March 4, 2000
Chromosome 22-specific low copy repeats and the 22q11.2 deletion syndrome: genomic organization and deletion endpoint analysis
T H Shaikh, H Kurahashi, S C Saitta, et al.
Human Molecular Genetics
|
March 1, 1997
Disruption of the clathrin heavy chain-like gene (CLTCL) associated with features of DGS/VCFS: a balanced (21;22)(p12;q11) translocation
S E Holmes, M A Riazi, W Gong, et al.
Genomics
|
July 15, 1996
Regional localization of over 300 loci on human chromosome 22 using a somatic cell hybrid mapping panel
M L Budarf, B Eckman, D Michaud, et al.
Genes and Immunity
|
October 22, 2010
A targeted association study in systemic lupus erythematosus identifies multiple susceptibility alleles
M L Budarf, P Goyette, G Boucher, et al.
Page
of 6