Babovic-Vuksanovic D - Search Results

1

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

2

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

3

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

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

Characteristics of two cases with dup(15)(q11.2-q12): one of maternal and one of paternal origin.

Mao R, Jalal SM, Snow K, Michels VV, Szabo SM, Babovic-Vuksanovic D. Mao R, et al. Genet Med. 2000 Mar-Apr;2(2):131-5. doi: 10.1097/00125817-200003000-00003. Genet Med. 2000. PMID: 11397326 Free article. Review.

6

Mosaic r(13) resulting in large deletion of chromosome 13q in a newborn female with multiple congenital anomalies.

Lorentz CP, Jalal SM, Thompson DM, Babovic-Vuksanovic D. Lorentz CP, et al. Am J Med Genet. 2002 Jul 22;111(1):61-7. doi: 10.1002/ajmg.10457. Am J Med Genet. 2002. PMID: 12124737 Review.

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

Subtelomeric deletion of 18p in an adult with paranoid schizophrenia and mental retardation.

Babovic-Vuksanovic D, Jenkins SC, Ensenauer R, Newman DC, Jalal SM. Babovic-Vuksanovic D, et al. Am J Med Genet A. 2004 Jan 30;124A(3):318-22. doi: 10.1002/ajmg.a.20391. Am J Med Genet A. 2004. PMID: 14708108

9

Unbalanced cryptic 5p deletion/17p duplication identified by subtelomeric FISH in a family with a boy with chimerism and a balanced t(4;5).

Ensenauer R, Jalal S, Meyer R, Babovic-Vuksanovic D. Ensenauer R, et al. Am J Med Genet A. 2004 Feb 15;125A(1):86-91. doi: 10.1002/ajmg.a.20420. Am J Med Genet A. 2004. PMID: 14755472

10

14q32.3 deletion syndrome with autism.

Merritt JL 2nd, Jalal SM, Barbaresi WJ, Babovic-Vuksanovic D. Merritt JL 2nd, et al. Am J Med Genet A. 2005 Feb 15;133A(1):99-100. doi: 10.1002/ajmg.a.30462. Am J Med Genet A. 2005. PMID: 15657934 No abstract available.

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