Litt M - Search Results

1

Further localization of a gene for paroxysmal dystonic choreoathetosis to a 5-cM region on chromosome 2q34.

Raskind WH, Bolin T, Wolff J, Fink J, Matsushita M, Litt M, Lipe H, Bird TD. Raskind WH, et al. Among authors: litt m. Hum Genet. 1998 Jan;102(1):93-7. doi: 10.1007/s004390050659. Hum Genet. 1998. PMID: 9490305 Free article.

2

Gender difference in apolipoprotein E-associated risk for familial Alzheimer disease: a possible clue to the higher incidence of Alzheimer disease in women.

Payami H, Zareparsi S, Montee KR, Sexton GJ, Kaye JA, Bird TD, Yu CE, Wijsman EM, Heston LL, Litt M, Schellenberg GD. Payami H, et al. Among authors: litt m. Am J Hum Genet. 1996 Apr;58(4):803-11. Am J Hum Genet. 1996. PMID: 8644745 Free PMC article.

3

A gene for episodic ataxia/myokymia maps to chromosome 12p13.

Litt M, Kramer P, Browne D, Gancher S, Brunt ER, Root D, Phromchotikul T, Dubay CJ, Nutt J. Litt M, et al. Am J Hum Genet. 1994 Oct;55(4):702-9. Am J Hum Genet. 1994. PMID: 7942848 Free PMC article.

4

Autosomal dominant congenital cataract associated with a missense mutation in the human alpha crystallin gene CRYAA.

Litt M, Kramer P, LaMorticella DM, Murphey W, Lovrien EW, Weleber RG. Litt M, et al. Hum Mol Genet. 1998 Mar;7(3):471-4. doi: 10.1093/hmg/7.3.471. Hum Mol Genet. 1998. PMID: 9467006

5

Genetic linkage is excluded for the D2-dopamine receptor lambda HD2G1 and flanking loci on chromosome 11q22-q23 in Tourette syndrome.

Devor EJ, Grandy DK, Civelli O, Litt M, Burgess AK, Isenberg KE, van de Wetering BJ, Oostra B. Devor EJ, et al. Among authors: litt m. Hum Hered. 1990;40(2):105-8. doi: 10.1159/000153914. Hum Hered. 1990. PMID: 2335364

6

A microsatellite-based index map of human chromosome 11.

Litt M, Kramer P, Hauge XY, Weber JL, Wang Z, Wilkie PJ, Holt MS, Mishra S, Donis-Keller H, Warnich L, et al. Litt M, et al. Hum Mol Genet. 1993 Jul;2(7):909-13. doi: 10.1093/hmg/2.7.909. Hum Mol Genet. 1993. PMID: 8364573

7

Localization of the autosomal dominant HLA-linked spinocerebellar ataxia (SCA1) locus, in two kindreds, within an 8-cM subregion of chromosome 6p.

Ranum LP, Duvick LA, Rich SS, Schut LJ, Litt M, Orr HT. Ranum LP, et al. Among authors: litt m. Am J Hum Genet. 1991 Jul;49(1):31-41. Am J Hum Genet. 1991. PMID: 1676561 Free PMC article.

8

Linkage disequilibria between pairs of loci within a highly polymorphic region of chromosome 2Q.

Litt M, Jorde LB. Litt M, et al. Am J Hum Genet. 1986 Aug;39(2):166-78. Am J Hum Genet. 1986. PMID: 3019131 Free PMC article.

9

A high resolution CEPH crossover mapping panel and integrated map of chromosome 11.

Fain PR, Kort EN, Yousry C, James MR, Litt M. Fain PR, et al. Among authors: litt m. Hum Mol Genet. 1996 Oct;5(10):1631-6. doi: 10.1093/hmg/5.10.1631. Hum Mol Genet. 1996. PMID: 8894699

10

The gene for autosomal dominant spinocerebellar ataxia (SCA1) maps telomeric to the HLA complex and is closely linked to the D6S89 locus in three large kindreds.

Zoghbi HY, Jodice C, Sandkuijl LA, Kwiatkowski TJ Jr, McCall AE, Huntoon SA, Lulli P, Spadaro M, Litt M, Cann HM, et al. Zoghbi HY, et al. Among authors: litt m. Am J Hum Genet. 1991 Jul;49(1):23-30. Am J Hum Genet. 1991. PMID: 2063871 Free PMC article.

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