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Biochimica Et Biophysica Acta
|
December 5, 1998
cDNA sequence and chromosomal localization of mouse Dlgh3 gene adjacent to the BRCA1 tumor suppressor locus
L Lin, L L Peters, S L Ciciotte, et al.
Genomics
|
June 15, 1997
The gene encoding protein 4.2 is distinct from the mouse platelet storage pool deficiency mutation pallid
B Gwynn, C Korsgren, C M Cohen, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society
|
December 22, 1999
The mouse adducin gene family: alternative splicing and chromosomal localization
S P Suriyapperuma, L Lozovatsky, S L Ciciotte, et al.
Genomics
|
January 7, 1998
Limatin (LIMAB1), an actin-binding LIM protein, maps to mouse chromosome 19 and human chromosome 10q25, a region frequently deleted in human cancers
A C Kim, L L Peters, J H Knoll, et al.
Blood
|
December 9, 2000
Defects in the cappuccino (cno) gene on mouse chromosome 5 and human 4p cause Hermansky-Pudlak syndrome by an AP-3-independent mechanism
B Gwynn, S L Ciciotte, S J Hunter, et al.
Page
of 1
Search research articles
Search
Showing results (1-10 of 5) with videos related to
Sort By:
Page
of 1
Biochimica Et Biophysica Acta
|
December 5, 1998
cDNA sequence and chromosomal localization of mouse Dlgh3 gene adjacent to the BRCA1 tumor suppressor locus
L Lin, L L Peters, S L Ciciotte, et al.
Genomics
|
June 15, 1997
The gene encoding protein 4.2 is distinct from the mouse platelet storage pool deficiency mutation pallid
B Gwynn, C Korsgren, C M Cohen, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society
|
December 22, 1999
The mouse adducin gene family: alternative splicing and chromosomal localization
S P Suriyapperuma, L Lozovatsky, S L Ciciotte, et al.
Genomics
|
January 7, 1998
Limatin (LIMAB1), an actin-binding LIM protein, maps to mouse chromosome 19 and human chromosome 10q25, a region frequently deleted in human cancers
A C Kim, L L Peters, J H Knoll, et al.
Blood
|
December 9, 2000
Defects in the cappuccino (cno) gene on mouse chromosome 5 and human 4p cause Hermansky-Pudlak syndrome by an AP-3-independent mechanism
B Gwynn, S L Ciciotte, S J Hunter, et al.
Page
of 1