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American Journal of Human Genetics|February 13, 2004
Oculocutaneous albinism type 4 is one of the most common types of albinism in JapanKatsuhiko Inagaki, Tamio Suzuki, Hiroshi Shimizu, et al.American Journal of Human Genetics|March 26, 2004
Phylogeographic analysis of haplogroup E3b (E-M215) y chromosomes reveals multiple migratory events within and out of AfricaFulvio Cruciani, Roberta La Fratta, Piero Santolamazza, et al.American Journal of Human Genetics|March 26, 2004
Bietti crystalline corneoretinal dystrophy is caused by mutations in the novel gene CYP4V2Anren Li, Xiaodong Jiao, Francis L Munier, et al.American Journal of Human Genetics|September 28, 2004
Family-based association study of synapsin II and schizophreniaQi Chen, Guang He, Wei Qin, et al.American Journal of Human Genetics|March 1, 1992
A truncated dystrophin lacking the C-terminal domains is localized at the muscle membraneT R Helliwell, J M Ellis, R C Mountford, et al.American Journal of Human Genetics|March 1, 1992
Detection of multiallele polymorphisms within gene sequences by GC-clamped denaturing gradient gel electrophoresisV C Sheffield, J S Beck, B Nichols, et al.American Journal of Human Genetics|March 1, 1992
Comparison of a multipoint identity-by-descent method with parametric multipoint linkage analysis for mapping quantitative traitsD E Goldgar, R S OnikiAmerican Journal of Human Genetics|June 1, 1992
Evidence for genetic heterogeneity of malignant hyperthermia susceptibilityT Deufel, A Golla, D Iles, et al.American Journal of Human Genetics|June 1, 1992
Detection and characterization of point mutations in the choroideremia candidate gene by PCR-SSCP analysis and direct DNA sequencingJ A van den Hurk, T J van de Pol, C M Molloy, et al.American Journal of Human Genetics|June 1, 1992
Linkage of familial breast cancer to chromosome 17q21 may not be restricted to early-onset diseaseP Margaritte, C Bonaiti-Pellie, M C King, et al.Pageof 980