Pericak-Vance MA - Search Results

1

Complete genomic screen for disease susceptibility loci in nuclear families.

Anderson JL, Hauser ER, Martin ER, Scott WK, Ashley-Koch A, Kim KJ, Monks SA, Haynes CS, Speer MC, Pericak-Vance MA. Anderson JL, et al. Genet Epidemiol. 1999;17 Suppl 1:S473-8. doi: 10.1002/gepi.1370170776. Genet Epidemiol. 1999. PMID: 10597478

2

Multilocus mapping of the X-linked hypophosphatemic rickets gene.

Econs MJ, Barker DF, Speer MC, Pericak-Vance MA, Fain PR, Drezner MK. Econs MJ, et al. J Clin Endocrinol Metab. 1992 Jul;75(1):201-6. doi: 10.1210/jcem.75.1.1352307. J Clin Endocrinol Metab. 1992. PMID: 1352307

3

Support of linkage of Gerstmann-Sträussler-Scheinker syndrome to the prion protein gene on chromosome 20p12-pter.

Speer MC, Goldgaber D, Goldfarb LG, Roses AD, Pericak-Vance MA. Speer MC, et al. Genomics. 1991 Feb;9(2):366-8. doi: 10.1016/0888-7543(91)90266-h. Genomics. 1991. PMID: 1672296

4

MspI RFLP for microtubule associated protein-2 (MAP2).

Alberts MJ, Kandt RS, Pericak-Vance MA, Bebout J, Speer MC, Siddique TS, Yamaoka L, Hung WY, Gaskell PC, Roses AD. Alberts MJ, et al. Nucleic Acids Res. 1991 Feb 25;19(4):960. doi: 10.1093/nar/19.4.960. Nucleic Acids Res. 1991. PMID: 1708129 Free PMC article.

5

Segregation analysis in cutaneous malignant melanoma/dysplastic nevus syndrome families.

Speer MC, Haynes CS, Pericak-Vance MA. Speer MC, et al. Cytogenet Cell Genet. 1992;59(2-3):225-7. doi: 10.1159/000133254. Cytogenet Cell Genet. 1992. PMID: 1737509 No abstract available.

6

A StuI polymorphism on chromosome 3p14.1-14.2 (D3S622) defined by two polymorphic StuI sites 2.4 kb apart.

Secore SL, Walker AP, Herbstreith MH, Siddique T, Jeffers AJ, DeShields TR, Speer MC, Pericak-Vance MA, Golembieski WA, Smith DI, et al. Secore SL, et al. Nucleic Acids Res. 1991 Nov 25;19(22):6349. doi: 10.1093/nar/19.22.6349. Nucleic Acids Res. 1991. PMID: 1956809 Free PMC article. No abstract available.

7

Linkage of a gene causing familial amyotrophic lateral sclerosis to chromosome 21 and evidence of genetic-locus heterogeneity.

Siddique T, Figlewicz DA, Pericak-Vance MA, Haines JL, Rouleau G, Jeffers AJ, Sapp P, Hung WY, Bebout J, McKenna-Yasek D, et al. Siddique T, et al. N Engl J Med. 1991 May 16;324(20):1381-4. doi: 10.1056/NEJM199105163242001. N Engl J Med. 1991. PMID: 2020294 Free article.

8

Linkage studies in tuberous sclerosis. Chromosome 9?, 11?, or maybe 14!

Kandt RS, Pericak-Vance MA, Hung WY, Gardner RJ, Crossen PE, Nellist MD, Speer MC, Roses AD. Kandt RS, et al. Ann N Y Acad Sci. 1991;615:284-97. doi: 10.1111/j.1749-6632.1991.tb37770.x. Ann N Y Acad Sci. 1991. PMID: 2039152

9

The human glycine receptor: a new probe that is linked to the X-linked hypophosphatemic rickets gene.

Econs MJ, Pericak-Vance MA, Betz H, Bartlett RJ, Speer MC, Drezner MK. Econs MJ, et al. Genomics. 1990 Jul;7(3):439-41. doi: 10.1016/0888-7543(90)90180-3. Genomics. 1990. PMID: 2163973

10

Linkage studies of late-onset familial Alzheimer's disease.

Roses AD, Pericak-Vance MA, Clark CM, Gilbert JR, Yamaoka LH, Haynes CS, Speer MC, Gaskell PC, Hung WY, Trofatter JA, et al. Roses AD, et al. Adv Neurol. 1990;51:185-96. Adv Neurol. 1990. PMID: 2294655 No abstract available.

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