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American Journal of Human Genetics|December 1, 1991
Statistical methods for multipoint radiation hybrid mappingM Boehnke, K Lange, D R CoxAmerican Journal of Human Genetics|December 1, 1991
The genetic and environmental sources of body mass index variability: the Muscatine Ponderosity Family StudyP P Moll, T L Burns, R M LauerAmerican Journal of Human Genetics|December 1, 1991
Consistent linkage of the long-QT syndrome to the Harvey ras-1 locus on chromosome 11M Keating, C Dunn, D Atkinson, et al.American Journal of Human Genetics|December 1, 1991
Adrenoleukodystrophy: a complex chromosomal rearrangement in the Xq28 red/green-color-pigment gene region indicates two possible gene localizationsR Feil, P Aubourg, J Mosser, et al.American Journal of Human Genetics|January 1, 1991
Four chromosomal breakpoints and four new probes mark out a 10-cM region encompassing the fragile-X locus (FRAXA)F Rousseau, A Vincent, S Rivella, et al.American Journal of Human Genetics|January 11, 1991
Waardenburg syndrome (WS): the analysis of a single family with a WS1 mutation showing linkage to RFLP markers on human chromosome 2qJ H Asher, R Morell, T B FriedmanAmerican Journal of Human Genetics|March 1, 1991
Clinical and molecular diagnosis of Miller-Dieker syndromeW B Dobyns, C J Curry, H E Hoyme, et al.American Journal of Human Genetics|May 1, 1991
Allele-specific hypermethylation of the retinoblastoma tumor-suppressor geneT Sakai, J Toguchida, N Ohtani, et al.American Journal of Human Genetics|April 1, 1991
A human gene homologous to the formin gene residing at the murine limb deformity locus: chromosomal location and RFLPsR L Maas, L I Jepeal, S L Elfering, et al.American Journal of Human Genetics|April 1, 1991
Analysis of the relationship of von Willebrand disease (vWD) and hereditary hemorrhagic telangiectasia and identification of a potential type IIA vWD mutation (IIe865 to Thr)M C Iannuzzi, N Hidaka, M Boehnke, et al.Pageof 979