Michels VV - Search Results

1

Linkage of nonspecific X-linked mental retardation to Xq21.31.

Jedele KB, Michels VV, Schaid DJ, Schowalter KV, Thibodeau SN. Jedele KB, et al. Among authors: michels vv. Am J Med Genet. 1992 Apr 15-May 1;43(1-2):436-42. doi: 10.1002/ajmg.1320430166. Am J Med Genet. 1992. PMID: 1605223

2

Autosomal dominant supravalvular aortic stenosis: localization to chromosome 7.

Olson TM, Michels VV, Lindor NM, Pastores GM, Weber JL, Schaid DJ, Driscoll DJ, Feldt RH, Thibodeau SN. Olson TM, et al. Among authors: michels vv. Hum Mol Genet. 1993 Jul;2(7):869-73. doi: 10.1093/hmg/2.7.869. Hum Mol Genet. 1993. PMID: 8364568

3

Uniparental disomy in congenital disorders: a prospective study.

Lindor NM, Karnes PS, Michels VV, Dewald GW, Goerss J, Jalal S, Jenkins RB, Vockley G, Thibodeau SN. Lindor NM, et al. Among authors: michels vv. Am J Med Genet. 1995 Aug 28;58(2):143-6. doi: 10.1002/ajmg.1320580210. Am J Med Genet. 1995. PMID: 8533805

4

Exclusion of a primary gene defect at the HLA locus in familial idiopathic dilated cardiomyopathy.

Olson TM, Thibodeau SN, Lundquist PA, Schaid DJ, Michels VV. Olson TM, et al. Among authors: michels vv. J Med Genet. 1995 Nov;32(11):876-80. doi: 10.1136/jmg.32.11.876. J Med Genet. 1995. PMID: 8592331 Free PMC article.

5

Exclusion of calcitonin/alpha-CGRP gene defect in a family with autosomal dominant supravalvular aortic stenosis.

Pastores GM, Michels VV, Schaid DJ, Driscoll DJ, Feldt RH, Thibodeau SN. Pastores GM, et al. Among authors: michels vv. J Med Genet. 1992 Jan;29(1):56-7. doi: 10.1136/jmg.29.1.56. J Med Genet. 1992. PMID: 1552547 Free PMC article. No abstract available.

6

Familial dermographism.

Jedele KB, Michels VV. Jedele KB, et al. Among authors: michels vv. Am J Med Genet. 1991 May 1;39(2):201-3. doi: 10.1002/ajmg.1320390216. Am J Med Genet. 1991. PMID: 2063925

7

Frequency of congenital heart defects in patients with hemophilia.

Jedele KB, Michels VV, Gordon H, Gilchrist GS. Jedele KB, et al. Among authors: michels vv. Am J Med Genet. 1990 Jul;36(3):333-5. doi: 10.1002/ajmg.1320360318. Am J Med Genet. 1990. PMID: 2363433

8

Carrier identification of cystic fibrosis by recombinant DNA techniques.

Dawson DB, Cummins LA, Schaid DJ, Michels VV, Gordon H, O'Connell EJ, Thibodeau SN. Dawson DB, et al. Among authors: michels vv. Mayo Clin Proc. 1989 Mar;64(3):325-34. doi: 10.1016/s0025-6196(12)65252-5. Mayo Clin Proc. 1989. PMID: 2564899 Review.

9

Rothmund-Thomson syndrome in siblings: evidence for acquired in vivo mosaicism.

Lindor NM, Devries EM, Michels VV, Schad CR, Jalal SM, Donovan KM, Smithson WA, Kvols LK, Thibodeau SN, Dewald GW. Lindor NM, et al. Among authors: michels vv. Clin Genet. 1996 Mar;49(3):124-9. doi: 10.1111/j.1399-0004.1996.tb03270.x. Clin Genet. 1996. PMID: 8737976

10

A novel mutation in KVLQT1 is the molecular basis of inherited long QT syndrome in a near-drowning patient's family.

Ackerman MJ, Schroeder JJ, Berry R, Schaid DJ, Porter CJ, Michels VV, Thibodeau SN. Ackerman MJ, et al. Among authors: michels vv. Pediatr Res. 1998 Aug;44(2):148-53. doi: 10.1203/00006450-199808000-00002. Pediatr Res. 1998. PMID: 9702906

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