Towbin JA - Search Results

1

Construction of a high-resolution physical map of the chromosome 10q22-q23 dilated cardiomyopathy locus and analysis of candidate genes.

Bowles KR, Abraham SE, Brugada R, Zintz C, Comeaux J, Sorajja D, Tsubata S, Li H, Brandon L, Gibbs RA, Scherer SE, Bowles NE, Towbin JA. Bowles KR, et al. Among authors: towbin ja. Genomics. 2000 Jul 15;67(2):109-27. doi: 10.1006/geno.2000.6242. Genomics. 2000. PMID: 10903836

2

Identification of new markers in Xp21 between DXS28 (C7) and DMD.

Worley KC, Towbin JA, Zhu XM, Barker DF, Ballabio A, Chamberlain J, Biesecker LG, Blethen SL, Brosnan P, Fox JE, et al. Worley KC, et al. Among authors: towbin ja. Genomics. 1992 Aug;13(4):957-61. doi: 10.1016/0888-7543(92)90007-f. Genomics. 1992. PMID: 1505987 Free article.

3

DXS28 (C7) maps centromeric to DXS68 (L1-4) and DXS67 (B24) by deletion analysis.

Towbin JA, Chamberlain JS, Wu DR, Pillers DA, Seltzer WK, McCabe ER. Towbin JA, et al. Genomics. 1990 Jul;7(3):442-4. doi: 10.1016/0888-7543(90)90181-s. Genomics. 1990. PMID: 2163974

4

Genetic basis of inherited cardiomyopathies.

Schowengerdt KO Jr, Towbin JA. Schowengerdt KO Jr, et al. Among authors: towbin ja. Curr Opin Cardiol. 1995 May;10(3):312-21. doi: 10.1097/00001573-199505000-00013. Curr Opin Cardiol. 1995. PMID: 7612983 Review.

5

Two long QT syndrome loci map to chromosomes 3 and 7 with evidence for further heterogeneity.

Jiang C, Atkinson D, Towbin JA, Splawski I, Lehmann MH, Li H, Timothy K, Taggart RT, Schwartz PJ, Vincent GM, et al. Jiang C, et al. Among authors: towbin ja. Nat Genet. 1994 Oct;8(2):141-7. doi: 10.1038/ng1094-141. Nat Genet. 1994. PMID: 7842012

6

Evidence of genetic heterogeneity in Romano-Ward long QT syndrome. Analysis of 23 families.

Towbin JA, Li H, Taggart RT, Lehmann MH, Schwartz PJ, Satler CA, Ayyagari R, Robinson JL, Moss A, Hejtmancik JF. Towbin JA, et al. Circulation. 1994 Dec;90(6):2635-44. doi: 10.1161/01.cir.90.6.2635. Circulation. 1994. PMID: 7994803

7

Yeast artificial chromosome cloning in the glycerol kinase and adrenal hypoplasia congenita region of Xp21.

Worley KC, Ellison KA, Zhang YH, Wang DF, Mason J, Roth EJ, Adams V, Fogt DD, Zhu XM, Towbin JA, et al. Worley KC, et al. Among authors: towbin ja. Genomics. 1993 May;16(2):407-16. doi: 10.1006/geno.1993.1204. Genomics. 1993. PMID: 8314578

8

Molecular genetic aspects of cardiomyopathy.

Towbin JA. Towbin JA. Biochem Med Metab Biol. 1993 Jun;49(3):285-320. doi: 10.1006/bmmb.1993.1032. Biochem Med Metab Biol. 1993. PMID: 8347375 Review.

9

X-linked dilated cardiomyopathy. Molecular genetic evidence of linkage to the Duchenne muscular dystrophy (dystrophin) gene at the Xp21 locus.

Towbin JA, Hejtmancik JF, Brink P, Gelb B, Zhu XM, Chamberlain JS, McCabe ER, Swift M. Towbin JA, et al. Circulation. 1993 Jun;87(6):1854-65. doi: 10.1161/01.cir.87.6.1854. Circulation. 1993. PMID: 8504498

10

Gene mapping of familial autosomal dominant dilated cardiomyopathy to chromosome 10q21-23.

Bowles KR, Gajarski R, Porter P, Goytia V, Bachinski L, Roberts R, Pignatelli R, Towbin JA. Bowles KR, et al. Among authors: towbin ja. J Clin Invest. 1996 Sep 15;98(6):1355-60. doi: 10.1172/JCI118922. J Clin Invest. 1996. PMID: 8823300 Free PMC article.

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