Michels VV - Search Results

1

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

2

Trisomy 9 mosaicism in a child with a tethered cord.

Lindor NM, Michels VV, Jalal S, Shaughnessy W. Lindor NM, et al. Among authors: michels vv. Clin Dysmorphol. 1995 Apr;4(2):169-72. Clin Dysmorphol. 1995. PMID: 7606325

3

Absence of chromosome fragility at 19q13.3 in patients with myotonic dystrophy.

Jalal SM, Lindor NM, Michels VV, Buckley DD, Hoppe DA, Sarkar G, Dewald GW. Jalal SM, et al. Among authors: michels vv. Am J Med Genet. 1993 Jun 1;46(4):441-3. doi: 10.1002/ajmg.1320460419. Am J Med Genet. 1993. PMID: 8357018

4

Maternal cell contamination of buccal smear samples in nursing neonates.

Babovic-Vuksanovic D, Michels VV, Law ME, Lindor NM, Jalal SM. Babovic-Vuksanovic D, et al. Among authors: michels vv. Clin Genet. 1998 Feb;53(2):114-8. doi: 10.1111/j.1399-0004.1998.tb02657.x. Clin Genet. 1998. PMID: 9611071

5

Xp22.3 microdeletion syndrome with microphthalmia, sclerocornea, linear skin defects, and congenital heart defects.

Lindor NM, Michels VV, Hoppe DA, Driscoll DJ, Leavitt JA, Dewald GW. Lindor NM, et al. Among authors: michels vv. Am J Med Genet. 1992 Sep 1;44(1):61-5. doi: 10.1002/ajmg.1320440115. Am J Med Genet. 1992. PMID: 1519653

6

Utility of subtelomeric fluorescent DNA probes for detection of chromosome anomalies in 425 patients.

Jalal SM, Harwood AR, Sekhon GS, Pham Lorentz C, Ketterling RP, Babovic-Vuksanovic D, Meyer RG, Ensenauer R, Anderson MH Jr, Michels VV. Jalal SM, et al. Among authors: michels vv. Genet Med. 2003 Jan-Feb;5(1):28-34. doi: 10.1097/00125817-200301000-00005. Genet Med. 2003. PMID: 12544473 Free article.

7

Microduplication 22q11.2, an emerging syndrome: clinical, cytogenetic, and molecular analysis of thirteen patients.

Ensenauer RE, Adeyinka A, Flynn HC, Michels VV, Lindor NM, Dawson DB, Thorland EC, Lorentz CP, Goldstein JL, McDonald MT, Smith WE, Simon-Fayard E, Alexander AA, Kulharya AS, Ketterling RP, Clark RD, Jalal SM. Ensenauer RE, et al. Among authors: michels vv. Am J Hum Genet. 2003 Nov;73(5):1027-40. doi: 10.1086/378818. Epub 2003 Oct 2. Am J Hum Genet. 2003. PMID: 14526392 Free PMC article.

8

Mosaic ring 20 with no detectable deletion by FISH analysis: Characteristic seizure disorder and literature review.

Zou YS, Van Dyke DL, Thorland EC, Chhabra HS, Michels VV, Keefe JG, Lega MA, Feely MA, Uphoff TS, Jalal SM. Zou YS, et al. Among authors: michels vv. Am J Med Genet A. 2006 Aug 1;140(15):1696-706. doi: 10.1002/ajmg.a.31332. Am J Med Genet A. 2006. PMID: 16835934

9

Delineation of the cryptic 1qter deletion phenotype.

Merritt JL 2nd, Zou Y, Jalal SM, Michels VV. Merritt JL 2nd, et al. Among authors: michels vv. Am J Med Genet A. 2007 Mar 15;143A(6):599-603. doi: 10.1002/ajmg.a.31611. Am J Med Genet A. 2007. PMID: 17304549

10

DNA fluorescent probes for diagnosis of velocardiofacial and related syndromes.

Crifasi PA, Michels VV, Driscoll DJ, Jalal SM, Dewald GW. Crifasi PA, et al. Among authors: michels vv. Mayo Clin Proc. 1995 Dec;70(12):1148-53. doi: 10.4065/70.12.1148. Mayo Clin Proc. 1995. PMID: 7490915

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