Ott J - Search Results

1

Spastic paraplegia with iron deposits in the basal ganglia: a new X-linked mental retardation syndrome.

Arena JF, Schwartz C, Stevenson R, Lawrence L, Carpenter A, Duara R, Ledbetter D, Huang T, Lehner T, Ott J, et al. Arena JF, et al. Among authors: ott j. Am J Med Genet. 1992 Apr 15-May 1;43(1-2):479-90. doi: 10.1002/ajmg.1320430172. Am J Med Genet. 1992. PMID: 1605230

2

Short tandem repeat polymorphism linkage studies in a new family with X-linked mental retardation (MRX20).

Lazzarini A, Stenroos ES, Lehner T, McKoy V, Gold B, McCormack MK, Reid CS, Ott J, Johnson WG. Lazzarini A, et al. Among authors: ott j. Am J Med Genet. 1995 Jul 17;57(4):552-7. doi: 10.1002/ajmg.1320570407. Am J Med Genet. 1995. PMID: 7573127

3

Failure to find a chromosome 18 pericentric linkage in families with schizophrenia.

DeLisi LE, Lofthouse R, Lehner T, Morganti C, Vita A, Shields G, Bass N, Ott J, Crow TJ. DeLisi LE, et al. Among authors: ott j. Am J Med Genet. 1995 Dec 18;60(6):532-4. doi: 10.1002/ajmg.1320600609. Am J Med Genet. 1995. PMID: 8825890

4

Interpreting nonsignificant outcomes of heterogeneity tests in gene mapping.

Mérette C, Lehner T, Ott J. Mérette C, et al. Among authors: ott j. Am J Hum Genet. 1991 Dec;49(6):1381-4. Am J Hum Genet. 1991. PMID: 1746563 Free PMC article. No abstract available.

5

Preliminary ranking procedures for multilocus ordering based on radiation hybrid data.

Weeks DE, Lehner T, Ott J. Weeks DE, et al. Among authors: ott j. Cytogenet Cell Genet. 1992;59(2-3):125-7. doi: 10.1159/000133222. Cytogenet Cell Genet. 1992. PMID: 1737477 No abstract available.

6

Further evidence for linkage of Gilles de la Tourette syndrome (GTS) susceptibility loci on chromosomes 2p11, 8q22 and 11q23-24 in South African Afrikaners.

Simonic I, Nyholt DR, Gericke GS, Gordon D, Matsumoto N, Ledbetter DH, Ott J, Weber JL. Simonic I, et al. Among authors: ott j. Am J Med Genet. 2001 Mar 8;105(2):163-7. doi: 10.1002/ajmg.1192. Am J Med Genet. 2001. PMID: 11304830

7

Two new approaches toward linkage heterogeneity of FAD: two-locus models and age of onset as a discriminator.

Mérette C, Lehner T, Ott J. Mérette C, et al. Among authors: ott j. Genet Epidemiol. 1993;10(6):455-9. doi: 10.1002/gepi.1370100621. Genet Epidemiol. 1993. PMID: 8314043

8

Late onset autosomal dominant cerebellar ataxia. A family description and linkage analysis with the HLA system.

Arruda WO, Petzl-Erler ML, Cardoso MA, Lehner T, Ott J. Arruda WO, et al. Among authors: ott j. Arq Neuropsiquiatr. 1991 Sep;49(3):285-91. doi: 10.1590/s0004-282x1991000300009. Arq Neuropsiquiatr. 1991. PMID: 1807228

9

Bipolar disorder and linkage to Xq28.

Baron M, Straub RE, Lehner T, Endicott J, Ott J, Gilliam TC, Lerer B. Baron M, et al. Among authors: ott j. Nat Genet. 1994 Aug;7(4):461-2. doi: 10.1038/ng0894-461a. Nat Genet. 1994. PMID: 7951314 No abstract available.

10

Linkage analysis for a disease with a complex mode of inheritance in a simulated data set.

Lehner T, Sandkuyl LA, Ott J. Lehner T, et al. Among authors: ott j. Prog Clin Biol Res. 1989;329:141-6. Prog Clin Biol Res. 1989. PMID: 2622943 No abstract available.

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