Showing results (21-30 of 6,483) with videos related to
Sort By:
Pageof 649
Journal of Medical Genetics|February 5, 2002
Sensitivity of conformation sensitive gel electrophoresis in detecting mutations in Marfan syndrome and related conditionsJ Körkkö, I Kaitila, L Lönnqvist, et al.Journal of Medical Genetics|November 6, 2001
High resolution comparative genomic hybridisation in clinical cytogeneticsM Kirchhoff, H Rose, C LundsteenJournal of Medical Genetics|November 6, 2001
Coeliac disease in Williams syndromeA Giannotti, G Tiberio, M Castro, et al.Journal of Medical Genetics|June 19, 2002
Testing for osteogenesis imperfecta in cases of suspected non-accidental injuryA Marlowe, M G Pepin, P H ByersJournal of Medical Genetics|May 16, 2002
An MLH1 haplotype is over-represented on chromosomes carrying an HNPCC predisposing mutation in MLH1P Hutter, J Wijnen, C Rey-Berthod, et al.Journal of Medical Genetics|July 13, 2002
Linkage of otosclerosis to a third locus (OTSC3) on human chromosome 6p21.3-22.3W Chen, C A Campbell, G E Green, et al.Journal of Medical Genetics|August 6, 2002
Clinical and molecular features of the immunodysregulation, polyendocrinopathy, enteropathy, X linked (IPEX) syndromeR S Wildin, S Smyk-Pearson, A H FilipovichJournal of Medical Genetics|August 6, 2002
Cardiovascular manifestations in 75 patients with Williams syndromeM Eronen, M Peippo, A Hiippala, et al.Journal of Medical Genetics|December 1, 1975
Heterozygote detection in phenylketonuria. Measurement of discriminatory ability and interpretation of the phenylalanine loading test by determination of the heterozygote likelihood ratioA Westwood, D N RainePageof 649