Report of the committee on the constitution of chromosome 19ROPERS, H. H; PERICAK-VANCE, M. A.Cytogenetics and cell genetics. 1990, Vol 55, Num 1-4, pp 218-228, issn 0301-0171, 11 p.Conference Paper

Genetic susceptibility to Alzheimer diseasePERICAK-VANCE, M. A; HAINES, J. L.Trends in genetics (Regular ed.). 1995, Vol 11, Num 12, pp 504-508, issn 0168-9525Article

Genetic epidemiology of the susceptibility to leprosySHIELDS, E. D; RUSSEL, D. A; PERICAK-VANCE, M. A et al.The Journal of clinical investigation. 1987, Vol 79, Num 4, pp 1139-1143, issn 0021-9738Article

The ischemic exercise test in normal adults and in patients with weakness and crampsCOLEMAN, R. A; STAJICH, J. M; PACT, V. W et al.Muscle & nerve. 1986, Vol 9, Num 3, pp 216-221, issn 0148-639XArticle

Linkage of familial dilated cardiomyopathy with conduction defect and muscular dystrophy to chromosome 6q23MESSINA, D. N; SPEER, M. C; PERICAK-VANCE, M. A et al.American journal of human genetics. 1997, Vol 61, Num 4, pp 909-917, issn 0002-9297Article

Prognosis in familial amyotrophic lateral sclerosis : Progression and survival in patients with glu100gly and ala4val mutations in Cu,Zn superoxide dismutaseJUNEJA, T; PERICAK-VANCE, M. A; LAING, N. G et al.Neurology. 1997, Vol 48, Num 1, pp 55-57, issn 0028-3878Article

Phenotypic heterogeneity in families with age-related macular degenerationDE LA PAZ, M. A; PERICAK-VANCE, M. A; HAINES, J. L et al.American journal of ophthalmology. 1997, Vol 124, Num 3, pp 331-343, issn 0002-9394Article

Using neural networks as an aid in the determination of disease status : Comparison of clinical diagnosis to neural-network predictions in a pedigree with autosomal dominant limb-girdle muscular dystrophyFALK, C. T; GILCHRIST, J. M; PERICAK-VANCE, M. A et al.American journal of human genetics. 1998, Vol 62, Num 4, pp 941-949, issn 0002-9297Article

A novel mutation in the von Hippel-Landau geneLOEB, D. B; PERICAK-VANCE, M. A; STAJICH, J. M et al.Human molecular genetics (Print). 1994, Vol 3, Num 8, pp 1423-1424, issn 0964-6906Article

Exclusion of TIMP3 as a candidate locus in Age-Related macular degenerationDE LA PAZ, M. A; PERICAK-VANCE, M. A; LENNON, F et al.Investigative ophthalmology & visual science. 1997, Vol 38, Num 6, pp 1060-1065, issn 0146-0404Article

Familial spastic paraparesis : Evaluation of locus heterogeneity, anticipation, and haplotype mapping of the SPG4 locus on the short arm of chromosome 2RASKIND, W. H; PERICAK-VANCE, M. A; LENNON, F et al.American journal of medical genetics. 1997, Vol 74, Num 1, pp 26-36, issn 0148-7299Article

Promiscuous expression of myosin in myotonic dystrophyMOORE, G. E; ROSES, A. D; PERICAK-VANCE, M. A et al.Muscle & nerve. 1986, Vol 9, Num 4, pp 355-363, issn 0148-639XArticle

RFLPs at the D19S19 locus of human chromosome 19 linked to myotonic dystrophy (DM)ROSES, A. D; PERICAK-VANCE, M. A; ROSS, D. A et al.Nucleic acids research. 1986, Vol 14, Num 13, issn 0305-1048, 5569Article

Linkage localization of X-linked Charcot-Marie-Tooth diseaseBERGOFFEN, J; TROFATTER, J; PERICAK-VANCE, M. A et al.American journal of human genetics. 1993, Vol 52, Num 2, pp 312-318, issn 0002-9297Article

North Carolina macular dystrophy is assigned to chromosome 6SMALL, K. W; WEBER, J. L; ROSES, A et al.Genomics (San Diego, Calif.). 1992, Vol 13, Num 3, pp 681-685, issn 0888-7543Article

Support of linkage of Gerstmann-Sträussler-Scheinker syndrome to the prion protein gene on chromosome 20p12-pterSPEER, M. C; GOLDGABER, D; GOLDFARB, L. G et al.Genomics (San Diego, Calif.). 1991, Vol 9, Num 2, pp 366-368, issn 0888-7543, 3 p.Article

Segregation and linkage analysis of α-N-acetyl-D-glucosaminidase (NAG) levels in a black familyPERICAK-VANCE, M. A; VANCE, J. M; ELSTON, R. C et al.American journal of medical genetics. 1985, Vol 20, Num 2, pp 295-306, issn 0148-7299Article

Genotype-based association test for general pedigrees: The genotype-PDTMARTIN, E. R; BASS, M. P; GILBERT, J. R et al.Genetic epidemiology. 2003, Vol 25, Num 3, pp 203-213, issn 0741-0395, 11 p.Article

Mutation analysis of the TSC2 gene in an African-American familyKUMAR, A; KANDT, R. S; WOLPERT, C et al.Human molecular genetics (Print). 1995, Vol 4, Num 12, pp 2295-2298, issn 0964-6906Article

Multilocus mapping of the X-linked hypophosphatemic rickets geneECONS, M. J; BARKER, D. F; SPEER, M. C et al.The Journal of clinical endocrinology and metabolism. 1992, Vol 75, Num 1, pp 201-206, issn 0021-972XArticle

Duchenne muscular dystrophy: detection of deletion carriers by spectrophotometric densitometryLAING, N. G; SIDDIQUE, T; BARTLETT, R et al.Clinical genetics. 1989, Vol 35, Num 6, pp 393-398, issn 0009-9163, 6 p.Article

Lewy body and Alzheimer pathology in a family with the amyloid-β precursor protein APP717 gene mutationROSENBERG, C. K; PERICAK-VANCE, M. A; SAUNDERS, A. M et al.Acta neuropathologica. 2000, Vol 100, Num 2, pp 145-152, issn 0001-6322Article

A second-generation genomic screen for multiple sclerosisKENEALY, S. J; BABRON, M.-C; OKSENBERG, J. R et al.American journal of human genetics. 2004, Vol 75, Num 6, pp 1070-1078, issn 0002-9297, 9 p.Article

Analysis of linkage disequilibrium in γ-aminobutyric acid receptor subunit genes in autistic disorderMARTIN, E. R; MENOLD, M. M; WRIGHT, H. H et al.American journal of medical genetics. 2000, Vol 96, Num 1, pp 43-48, issn 0148-7299Article

Analysis of the Stargardt disease gene (ABCR) in age-related macular degenerationDE LA PAZ, M. A; GUY, V. K; ABOU-DONIA, S et al.Ophthalmology (Rochester, MN). 1999, Vol 106, Num 8, pp 1531-1536, issn 0161-6420Article