Dean M - Search Results

1

Mapping of a gene causing familial Mediterranean fever to the short arm of chromosome 16.

Pras E, Aksentijevich I, Gruberg L, Balow JE Jr, Prosen L, Dean M, Steinberg AD, Pras M, Kastner DL. Pras E, et al. Among authors: dean m. N Engl J Med. 1992 Jun 4;326(23):1509-13. doi: 10.1056/NEJM199206043262301. N Engl J Med. 1992. PMID: 1579134 Free article.

2

The gene causing familial Mediterranean fever maps to the short arm of chromosome 16 in Druze and Moslem Arab families.

Pras E, Aksentijevich I, Levy E, Gruberg L, Prosen L, Dean M, Pras M, Kastner DL. Pras E, et al. Among authors: dean m. Hum Genet. 1994 Nov;94(5):576-7. doi: 10.1007/BF00211032. Hum Genet. 1994. PMID: 7959700 No abstract available.

3

Familial Mediterranean fever (FMF) in Moroccan Jews: demonstration of a founder effect by extended haplotype analysis.

Aksentijevich I, Pras E, Gruberg L, Shen Y, Holman K, Helling S, Prosen L, Sutherland GR, Richards RI, Dean M, et al. Aksentijevich I, et al. Among authors: dean m. Am J Hum Genet. 1993 Sep;53(3):644-51. Am J Hum Genet. 1993. PMID: 8102507 Free PMC article.

4

Evidence for linkage of the gene causing familial Mediterranean fever to chromosome 17q in non-Ashkenazi Jewish families: second locus or type I error?

Aksentijevich I, Gruberg L, Pras E, Balow JE Jr, Kovo M, Gazit E, Dean M, Pras M, Kastner DL. Aksentijevich I, et al. Among authors: dean m. Hum Genet. 1993 Jul;91(6):527-34. doi: 10.1007/BF00205075. Hum Genet. 1993. PMID: 8340105

5

Localization of the gene for the nevoid basal cell carcinoma syndrome.

Goldstein AM, Stewart C, Bale AE, Bale SJ, Dean M. Goldstein AM, et al. Among authors: dean m. Am J Hum Genet. 1994 May;54(5):765-73. Am J Hum Genet. 1994. PMID: 7909984 Free PMC article.

6

Genetic mapping of the human tryptophan hydroxylase gene on chromosome 11, using an intronic conformational polymorphism.

Nielsen DA, Dean M, Goldman D. Nielsen DA, et al. Among authors: dean m. Am J Hum Genet. 1992 Dec;51(6):1366-71. Am J Hum Genet. 1992. PMID: 1463016 Free PMC article.

7

Mapping of the serotonin 5-HT1D beta autoreceptor gene on chromosome 6 and direct analysis for sequence variants.

Lappalainen J, Dean M, Charbonneau L, Virkkunen M, Linnoila M, Goldman D. Lappalainen J, et al. Among authors: dean m. Am J Med Genet. 1995 Apr 24;60(2):157-61. doi: 10.1002/ajmg.1320600214. Am J Med Genet. 1995. PMID: 7485252

8

Mapping of the serotonin 5-HT1D alpha autoreceptor gene (HTR1D) on chromosome 1 using a silent polymorphism in the coding region.

Ozaki N, Lappalainen J, Dean M, Virkkunen M, Linnoila M, Goldman D. Ozaki N, et al. Among authors: dean m. Am J Med Genet. 1995 Apr 24;60(2):162-4. doi: 10.1002/ajmg.1320600215. Am J Med Genet. 1995. PMID: 7485253 No abstract available.

9

Genetic mapping of the beta 1 GABA receptor gene to human chromosome 4, using a tetranucleotide repeat polymorphism.

Dean M, Lucas-Derse S, Bolos A, O'Brien SJ, Kirkness EF, Fraser CM, Goldman D. Dean M, et al. Am J Hum Genet. 1991 Sep;49(3):621-6. Am J Hum Genet. 1991. PMID: 1652891 Free PMC article.

10

Identification of the cystic fibrosis gene: chromosome walking and jumping.

Rommens JM, Iannuzzi MC, Kerem B, Drumm ML, Melmer G, Dean M, Rozmahel R, Cole JL, Kennedy D, Hidaka N, et al. Rommens JM, et al. Among authors: dean m. Science. 1989 Sep 8;245(4922):1059-65. doi: 10.1126/science.2772657. Science. 1989. PMID: 2772657

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