Varvil TS - Search Results

1

Genetic screening of candidate genes for a prothrombotic interaction with type I protein C deficiency in a large kindred.

Scott BT, Bovill EG, Callas PW, Hasstedt SJ, Leppert MF, Valliere JE, Varvil TS, Long GL. Scott BT, et al. Among authors: varvil ts. Thromb Haemost. 2001 Jan;85(1):82-7. Thromb Haemost. 2001. PMID: 11204593

2

Genetic susceptibility in familial multiple sclerosis not linked to the myelin basic protein gene.

Rose J, Gerken S, Lynch S, Pisani P, Varvil T, Otterud B, Leppert M. Rose J, et al. Lancet. 1993 May 8;341(8854):1179-81. doi: 10.1016/0140-6736(93)91003-5. Lancet. 1993. PMID: 7683738

3

Evaluation of heterodimeric guanylyl cyclase genes as candidates for human hypertension.

Danziger RS, Pappas C, Barnitz C, Varvil T, Hunt SC, Leppert MF. Danziger RS, et al. J Hypertens. 2000 Mar;18(3):263-6. doi: 10.1097/00004872-200018030-00004. J Hypertens. 2000. PMID: 10726711

4

Genome-wide linkage in Utah autism pedigrees.

Allen-Brady K, Robison R, Cannon D, Varvil T, Villalobos M, Pingree C, Leppert MF, Miller J, McMahon WM, Coon H. Allen-Brady K, et al. Mol Psychiatry. 2010 Oct;15(10):1006-15. doi: 10.1038/mp.2009.42. Epub 2009 May 19. Mol Psychiatry. 2010. PMID: 19455147 Free PMC article.

5

Linkage of a familial platelet disorder with a propensity to develop myeloid malignancies to human chromosome 21q22.1-22.2.

Ho CY, Otterud B, Legare RD, Varvil T, Saxena R, DeHart DB, Kohler SE, Aster JC, Dowton SB, Li FP, Leppert M, Gilliland DG. Ho CY, et al. Blood. 1996 Jun 15;87(12):5218-24. Blood. 1996. PMID: 8652836 Free article.

6

A locus for febrile seizures (FEB3) maps to chromosome 2q23-24.

Peiffer A, Thompson J, Charlier C, Otterud B, Varvil T, Pappas C, Barnitz C, Gruenthal K, Kuhn R, Leppert M. Peiffer A, et al. Ann Neurol. 1999 Oct;46(4):671-8. doi: 10.1002/1531-8249(199910)46:4<671::aid-ana20>3.0.co;2-5. Ann Neurol. 1999. PMID: 10514109

7

Molecular cloning and physical and genetic mapping of the human anion exchanger isoform 3 (SLC2C) gene to chromosome 2q36.

Su YR, Klanke CA, Houseal TW, Linn SC, Burk SE, Varvil TS, Otterud BE, Shull GE, Leppert MF, Menon AG. Su YR, et al. Among authors: varvil ts. Genomics. 1994 Aug;22(3):605-9. doi: 10.1006/geno.1994.1433. Genomics. 1994. PMID: 8001971

8

Paroxysmal dystonic choreoathetosis: tight linkage to chromosome 2q.

Fink JK, Rainer S, Wilkowski J, Jones SM, Kume A, Hedera P, Albin R, Mathay J, Girbach L, Varvil T, Otterud B, Leppert M. Fink JK, et al. Am J Hum Genet. 1996 Jul;59(1):140-5. Am J Hum Genet. 1996. PMID: 8659518 Free PMC article.

9

Dinucleotide repeat polymorphism from a cosmid containing the human anion exchanger isoform 3 (SLC2C) gene.

Klanke CA, Su YR, Varvil TS, Otterud BE, Leppert M, Menon AG. Klanke CA, et al. Among authors: varvil ts. Hum Mol Genet. 1994 Nov;3(11):2086. Hum Mol Genet. 1994. PMID: 7874147 No abstract available.

10

Autosomal dominant familial spastic paraplegia: tight linkage to chromosome 15q.

Fink JK, Wu CT, Jones SM, Sharp GB, Lange BM, Lesicki A, Reinglass T, Varvil T, Otterud B, Leppert M. Fink JK, et al. Am J Hum Genet. 1995 Jan;56(1):188-92. Am J Hum Genet. 1995. PMID: 7825577 Free PMC article.

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