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American Journal of Human Genetics|June 30, 2001
A novel frameshift mutation in exon 23 of ATP7A (MNK) results in occipital horn syndrome and not in Menkes diseaseS L Dagenais, A N Adam, J W Innis, et al.Gene|September 7, 2000
Isolation of a murine copper transporter gene, tissue specific expression and functional complementation of a yeast copper transport mutantJ Lee, J R Prohaska, S L Dagenais, et al.Genes, Chromosomes & Cancer|February 15, 2001
Translocation breakpoints in FHIT and FRA3B in both homologs of chromosome 3 in an esophageal adenocarcinomaJ M Fang, M F Arlt, A C Burgess, et al.American Journal of Human Genetics|November 15, 2000
Mutations in FOXC2 (MFH-1), a forkhead family transcription factor, are responsible for the hereditary lymphedema-distichiasis syndromeJ Fang, S L Dagenais, R P Erickson, et al.Cancer Research|August 12, 1998
The murine Fhit gene is highly similar to its human orthologue and maps to a common fragile site regionT W Glover, A W Hoge, D E Miller, et al.Journal of Medical Genetics|November 6, 2001
Clinical heterogeneity in lymphoedema-distichiasis with FOXC2 truncating mutationsR P Erickson, S L Dagenais, M S Caulder, et al.Pageof 1