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Genes, Chromosomes & Cancer|May 25, 1999
Severe phenotype of neurofibromatosis type 2 in a patient with a 7.4-MB constitutional deletion on chromosome 22: possible localization of a neurofibromatosis type 2 modifier gene?C E Bruder, K Ichimura, E Blennow, et al.Genes, Chromosomes & Cancer|June 1, 1994
Deletions on chromosome 22 in sporadic meningiomaM H Ruttledge, Y G Xie, F Y Han, et al.Human Genetics|March 1, 1994
Isolation and mapping of cosmid markers on human chromosome 22, including one within the submicroscopically deleted region of DiGeorge syndromeH Kurahashi, K Akagi, K Karakawa, et al.Genes, Chromosomes & Cancer|October 1, 1993
Regional fine mapping of the beta crystallin genes on chromosome 22 excludes these genes as physically linked markers for neurofibromatosis type 2E K Bijlsma, O Delattre, J A Juyn, et al.Human Genetics|August 21, 2001
The position of t(11;22)(q23;q11) constitutional translocation breakpoint is conserved among its carriersI Tapia-Páez, M Kost-Alimova, P Hu, et al.Human Genetics|July 8, 1999
A group of schwannomas with interstitial deletions on 22q located outside the NF2 locus shows no detectable mutations in the NF2 geneC E Bruder, K Ichimura, O Tingby, et al.Genes, Chromosomes & Cancer|September 17, 1998
Various regions within the alpha-helical domain of the COL1A1 gene are fused to the second exon of the PDGFB gene in dermatofibrosarcomas and giant-cell fibroblastomasK P O'Brien, E Seroussi, P Dal Cin, et al.Genome Research|October 6, 1999
Duplications on human chromosome 22 reveal a novel Ret Finger Protein-like gene family with sense and endogenous antisense transcriptsE Seroussi, D Kedra, H Q Pan, et al.Genomics|August 15, 1996
Structure of the promoter and genomic organization of the human beta'-adaptin gene (BAM22) from chromosome 22q12M Peyrard, H Q Pan, D Kedra, et al.Cancer Research|August 2, 2001
Growth inhibition of dermatofibrosarcoma protuberans tumors by the platelet-derived growth factor receptor antagonist STI571 through induction of apoptosisT Sjöblom, A Shimizu, K P O'Brien, et al.Pageof 7