Genetic disorders of pigmentationSPRITZ, R. A; HEARING, V. J.Advances in human genetics. 1994, Vol 22, pp 1-45, issn 0065-275XArticle

Marker (X)-linked mental retardationTURNER, G; JACOBS, P.Advances in human genetics. 1983, Vol 13, pp 83-112, issn 0065-275XArticle

Mutations affecting trace elements in humans and animals: a genetic approach to an understanding of trace elementsDANKS, D. M; CAMAKARIS, J.Advances in human genetics. 1983, Vol 13, pp 149-216, issn 0065-275XArticle

Peroxisomal diseasesMOSER, H. W.Advances in human genetics. 1993, Vol 21, pp 1-106, issn 0065-275XArticle

Genetic aspects of amyloidosisJACOBSON, D. R; BUXBAUM, J. N.Advances in human genetics. 1991, Vol 20, pp 69-123, issn 0065-275XArticle

Molecular genetics of von Recklinghausen neurofibromatosisWALLACE, M. R; COLLINS, F. S.Advances in human genetics. 1991, Vol 20, pp 267-307, issn 0065-275XArticle

Genetics of growth hormone and its disordersPHILLIPS, J. A; VNENCAK-JONES, C. L.Advances in human genetics. 1989, Vol 18, pp 305-363, issn 0065-275X, 59 p.Article

Trisomy 21: Molecular and cytogenetic studies of nondisjunctionSTEWART, G. D; HASSOLD, T. J; KURNIT, D. M et al.Advances in human genetics. 1988, Vol 17, pp 99-140, issn 0065-275XArticle

Genetic mutations affecting human lipoprotein metabolismZANNIS, V. I; BRESLOW, J. L.Advances in human genetics. 1985, Vol 14, pp 125-386, issn 0065-275XArticle

Molecular genetics of Charcot-Marie-Tooth neuropathyROA, B. B; LUPSKI, J. R.Advances in human genetics. 1994, Vol 22, pp 117-152, issn 0065-275XArticle

Nonisotopic in situ hybridization. Clinical cytogenetics and gene mapping applicationsADINOLFI, M; CROLLA, J.Advances in human genetics. 1994, Vol 22, pp 187-255, issn 0065-275XArticle

Gaucher disease. Enzymology, genetics, and treatmentGRABOWSKI, G. A.Advances in human genetics. 1993, Vol 21, pp 377-441, issn 0065-275XArticle

Biochemical and molecular genetics of cystic fibrosisLAP-CHEE TSUI; BUCHWALD, M.Advances in human genetics. 1991, Vol 20, pp 153-266, issn 0065-275XArticle

Huntington's diseaseGUSELLA, J. F.Advances in human genetics. 1991, Vol 20, pp 125-151, issn 0065-275XArticle

An algorithm for comparing two-dimensional electrophoretic gels, with particular reference to the study of mutationSKOLNICK, M. M; NELL, J. V.Advances in human genetics. 1986, Vol 15, pp 55-160, issn 0065-275XArticle

Genetic mutations affecting human lipoproteins, their receptors, and teir enzymesZANNIS, V. I; KARDASSIS, D; ECONOMOU ZANNI, E et al.Advances in human genetics. 1993, Vol 21, pp 145-319, issn 0065-275XArticle

Chromosome instability syndromesCOHEN, M. M; LEVY, H. P.Advances in human genetics. 1989, Vol 18, pp 43-149, issn 0065-275X, 114 p.Article

The molecular genetics of hemophilia A and B in man: Factor VIII and factor IX deficiencyANTONARAKIS, S. E.Advances in human genetics. 1988, Vol 17, pp 27-59, issn 0065-275XArticle

Genetics of lactose digestion in humansFLATZ, G.Advances in human genetics. 1987, Vol 16, pp 1-77, issn 0065-275XArticle

Cytogenetics of pregnancy wastageBOUE, A; BOUE, J; GROPP, A et al.Advances in human genetics. 1985, Vol 14, pp 1-57, issn 0065-275XArticle

Mutation in human populationsCROW, J. F; DENNISTON, C.Advances in human genetics. 1985, Vol 14, pp 59-123, issn 0065-275XArticle

Steroid sulfatase deficiency and the genetics of the short arm of the human X chromosomeSHAPIRO, L. J.Advances in human genetics. 1985, Vol 14, pp 331-389, issn 0065-275XArticle

Phenylketonuria and its variantsKAUFMAN, S.Advances in human genetics. 1983, Vol 13, pp 217-297, issn 0065-275XArticle

Lacticacidema: biochemical, clinical, and genetic considerationsROBINSON, B. H.Advances in human genetics. 1989, Vol 18, pp 151-179, issn 0065-275X, 31 p.Article

Cloning of the Duchenne/Becker muscular dystrophy locusMONACO, A. P; KUNKEL, L. M.Advances in human genetics. 1988, Vol 17, pp 61-98, issn 0065-275XArticle