Babovic-Vuksanovic D - Search Results

1

Connective tissue dysplasia in five new patients with NF1 microdeletions: further expansion of phenotype and review of the literature.

Mensink KA, Ketterling RP, Flynn HC, Knudson RA, Lindor NM, Heese BA, Spinner RJ, Babovic-Vuksanovic D. Mensink KA, et al. J Med Genet. 2006 Feb;43(2):e8. doi: 10.1136/jmg.2005.034256. J Med Genet. 2006. PMID: 16467218 Free PMC article. Review.

2

Visual impairment due to macular disciform scars in a 20-year-old man with Smith-Magenis syndrome: another ophthalmologic complication.

Babovic-Vuksanovic D, Jalal SM, Garrity JA, Robertson DM, Lindor NM. Babovic-Vuksanovic D, et al. Am J Med Genet. 1998 Dec 4;80(4):373-6. doi: 10.1002/(sici)1096-8628(19981204)80:4<373::aid-ajmg13>3.0.co;2-m. Am J Med Genet. 1998. PMID: 9856566

3

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. Clin Genet. 1998 Feb;53(2):114-8. doi: 10.1111/j.1399-0004.1998.tb02657.x. Clin Genet. 1998. PMID: 9611071

4

Guidelines for buccal smear collection in breast-fed infants.

Babovic-Vuksanovic D, Michels VV, Law ME, Bailey R, Wyatt WA, Lindor NM, Jalal SM. Babovic-Vuksanovic D, et al. Am J Med Genet. 1999 Jun 4;84(4):357-60. doi: 10.1002/(sici)1096-8628(19990604)84:4<357::aid-ajmg9>3.0.co;2-4. Am J Med Genet. 1999. PMID: 10340651

5

Paraspinal neurofibromas and hypertrophic neuropathy in Noonan syndrome with multiple lentigines.

Conboy E, Dhamija R, Wang M, Xie J, Dyck PJ, Bridges AG, Spinner RJ, Clayton AC, Watson RE, Messiaen L, Babovic-Vuksanovic D. Conboy E, et al. J Med Genet. 2016 Feb;53(2):123-6. doi: 10.1136/jmedgenet-2015-103177. Epub 2015 Sep 2. J Med Genet. 2016. PMID: 26337637

6

Bifid tongue, corneal clouding, and Dandy-Walker malformation in a male infant with otopalatodigital syndrome type 2.

Murphy-Ryan M, Babovic-Vuksanovic D, Lindor N. Murphy-Ryan M, et al. Am J Med Genet A. 2011 Apr;155A(4):855-9. doi: 10.1002/ajmg.a.33901. Epub 2011 Mar 15. Am J Med Genet A. 2011. PMID: 21412975

7

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. Genet Med. 2003 Jan-Feb;5(1):28-34. doi: 10.1097/00125817-200301000-00005. Genet Med. 2003. PMID: 12544473 Free article.

8

Clinical characteristics associated with dup17(q24q25.1) in a mosaic mother and two non-mosaic daughters.

Babovic-Vuksanovic D, Westman JA, Jalal SM, Lindor NM. Babovic-Vuksanovic D, et al. Clin Dysmorphol. 1998 Jul;7(3):171-6. doi: 10.1097/00019605-199807000-00003. Clin Dysmorphol. 1998. PMID: 9689989

9

Selective antibody immune deficiency in a patient with Smith-Lemli-Opitz syndrome.

Babovic-Vuksanovic D, Jacobson RM, Lindor NM, Weiler CR. Babovic-Vuksanovic D, et al. J Inherit Metab Dis. 2005;28(2):181-6. doi: 10.1007/s10545-005-5515-3. J Inherit Metab Dis. 2005. PMID: 15877207

10

Phase II trial of pirfenidone in adults with neurofibromatosis type 1.

Babovic-Vuksanovic D, Ballman K, Michels V, McGrann P, Lindor N, King B, Camp J, Micic V, Babovic N, Carrero X, Spinner R, O'Neill B. Babovic-Vuksanovic D, et al. Neurology. 2006 Nov 28;67(10):1860-2. doi: 10.1212/01.wnl.0000243231.12248.67. Epub 2006 Oct 11. Neurology. 2006. PMID: 17035676 Clinical Trial.

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