Seidman C - Search Results

1

Mutations in COCH (formerly Coch5b2) cause DFNA9.

Eavey RD, Manolis EN, Lubianca J, Merchant S, Seidman JG, Seidman C. Eavey RD, et al. Among authors: seidman jg, seidman c. Adv Otorhinolaryngol. 2000;56:101-2. doi: 10.1159/000059070. Adv Otorhinolaryngol. 2000. PMID: 10868220 No abstract available.

2

The gene responsible for familial hypocalciuric hypercalcemia maps to chromosome 3q in four unrelated families.

Chou YH, Brown EM, Levi T, Crowe G, Atkinson AB, Arnqvist HJ, Toss G, Fuleihan GE, Seidman JG, Seidman CE. Chou YH, et al. Among authors: seidman jg, seidman ce. Nat Genet. 1992 Jul;1(4):295-300. doi: 10.1038/ng0792-295. Nat Genet. 1992. PMID: 1302026

3

Sporadic hypertrophic cardiomyopathy due to de novo myosin mutations.

Watkins H, Thierfelder L, Hwang DS, McKenna W, Seidman JG, Seidman CE. Watkins H, et al. Among authors: seidman jg, seidman ce. J Clin Invest. 1992 Nov;90(5):1666-71. doi: 10.1172/JCI116038. J Clin Invest. 1992. PMID: 1430197 Free PMC article.

4

Characteristics and prognostic implications of myosin missense mutations in familial hypertrophic cardiomyopathy.

Watkins H, Rosenzweig A, Hwang DS, Levi T, McKenna W, Seidman CE, Seidman JG. Watkins H, et al. Among authors: seidman jg, seidman ce. N Engl J Med. 1992 Apr 23;326(17):1108-14. doi: 10.1056/NEJM199204233261703. N Engl J Med. 1992. PMID: 1552912 Free article.

5

cis-dominance of rat atrial natriuretic factor gene regulatory sequences in transgenic mice.

Seidman CE, Schmidt EV, Seidman JG. Seidman CE, et al. Among authors: seidman jg. Can J Physiol Pharmacol. 1991 Oct;69(10):1486-92. doi: 10.1139/y91-223. Can J Physiol Pharmacol. 1991. PMID: 1723347

6

Progress in familial hypertrophic cardiomyopathy: molecular genetic analyses in the original family studied by Teare.

Watkins H, Seidman CE, MacRae C, Seidman JG, McKenna W. Watkins H, et al. Among authors: seidman jg, seidman ce. Br Heart J. 1992 Jan;67(1):34-8. doi: 10.1136/hrt.67.1.34. Br Heart J. 1992. PMID: 1739523 Free PMC article. Review. No abstract available.

7

Mutations in cardiac myosin heavy chain genes cause familial hypertrophic cardiomyopathy.

Seidman CE, Seidman JG. Seidman CE, et al. Among authors: seidman jg. Mol Biol Med. 1991 Apr;8(2):159-66. Mol Biol Med. 1991. PMID: 1806760 Review.

8

Proximal regulatory domains of rat atrial natriuretic factor gene.

Rosenzweig A, Halazonetis TD, Seidman JG, Seidman CE. Rosenzweig A, et al. Among authors: seidman jg, seidman ce. Circulation. 1991 Sep;84(3):1256-65. doi: 10.1161/01.cir.84.3.1256. Circulation. 1991. PMID: 1832094

9

Preclinical diagnosis of familial hypertrophic cardiomyopathy by genetic analysis of blood lymphocytes.

Rosenzweig A, Watkins H, Hwang DS, Miri M, McKenna W, Traill TA, Seidman JG, Seidman CE. Rosenzweig A, et al. Among authors: seidman jg, seidman ce. N Engl J Med. 1991 Dec 19;325(25):1753-60. doi: 10.1056/NEJM199112193252501. N Engl J Med. 1991. PMID: 1944483 Free article.

10

A molecular basis for familial hypertrophic cardiomyopathy: a beta cardiac myosin heavy chain gene missense mutation.

Geisterfer-Lowrance AA, Kass S, Tanigawa G, Vosberg HP, McKenna W, Seidman CE, Seidman JG. Geisterfer-Lowrance AA, et al. Among authors: seidman jg, seidman ce. Cell. 1990 Sep 7;62(5):999-1006. doi: 10.1016/0092-8674(90)90274-i. Cell. 1990. PMID: 1975517

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