Velinov M - Search Results

1

Mild cognitive impairment identified in older individuals with Down syndrome by reduced telomere signal numbers and shorter telomeres measured in microns.

Jenkins EC, Ye L, Velinov M, Krinsky-McHale SJ, Zigman WB, Schupf N, Silverman WP. Jenkins EC, et al. Among authors: velinov m. Am J Med Genet B Neuropsychiatr Genet. 2012 Jul;159B(5):598-604. doi: 10.1002/ajmg.b.32066. Epub 2012 May 16. Am J Med Genet B Neuropsychiatr Genet. 2012. PMID: 22592955 Free PMC article.

2

The feasibility of PCR-based diagnosis of Prader-Willi and Angelman syndromes using restriction analysis after bisulfite modification of genomic DNA.

Velinov M, Gu H, Genovese M, Duncan C, Brown WT, Jenkins E. Velinov M, et al. Mol Genet Metab. 2000 Jan;69(1):81-3. doi: 10.1006/mgme.1999.2941. Mol Genet Metab. 2000. PMID: 10655162

3

PCR-based methylation testing for Prader-Willi or Angelman syndromes using archived fixed-cell suspensions.

Velinov M, Gu H, Shah K, Genovese M, Duncan C, Kupchik G, Jenkins EC. Velinov M, et al. Genet Test. 2001 Summer;5(2):153-5. doi: 10.1089/109065701753145655. Genet Test. 2001. PMID: 11551105

4

Hypoplastic left heart in a female infant with partial trisomy 4q due to de novo 4;21 translocation.

Velinov M, Gu H, Yeboa K, Warburton D, Tubo T, Dhuper S, Lanter S, Delprino D, Kupchik G, Jenkins EC. Velinov M, et al. Am J Med Genet. 2002 Feb 1;107(4):330-3. doi: 10.1002/ajmg.10140. Am J Med Genet. 2002. PMID: 11840491

5

PCR-based strategies for the diagnosis of Prader-Willi/Angelman syndromes.

Velinov M, Jenkins EC. Velinov M, et al. Methods Mol Biol. 2003;217:209-16. doi: 10.1385/1-59259-330-5:209. Methods Mol Biol. 2003. PMID: 12491935 No abstract available.

6

Characterization of an analphoid, neocentromere-positive inv dup 8p marker chromosome using multiplex whole chromosome and sub-telomere FISH analyses.

Velinov M, Gu H, Genovese M, Duncan C, Warburton P, Brooks SS, Jenkins EC. Velinov M, et al. Ann Genet. 2004 Apr-Jun;47(2):199-205. doi: 10.1016/j.anngen.2004.02.005. Ann Genet. 2004. PMID: 15183754

7

Polycystic kidneys and del (4)(q21.1q21.3): further delineation of a distinct phenotype.

Velinov M, Kupferman J, Gu H, Macera MJ, Babu A, Jenkins EC, Kupchik G. Velinov M, et al. Eur J Med Genet. 2005 Jan-Mar;48(1):51-5. doi: 10.1016/j.ejmg.2005.01.008. Epub 2005 Feb 12. Eur J Med Genet. 2005. PMID: 15953406

8

Telomere shortening in T lymphocytes of older individuals with Down syndrome and dementia.

Jenkins EC, Velinov MT, Ye L, Gu H, Li S, Jenkins EC Jr, Brooks SS, Pang D, Devenny DA, Zigman WB, Schupf N, Silverman WP. Jenkins EC, et al. Neurobiol Aging. 2006 Jul;27(7):941-5. doi: 10.1016/j.neurobiolaging.2005.05.021. Epub 2005 Jul 19. Neurobiol Aging. 2006. PMID: 16046031

9

Reduced telomere length in older men with premutation alleles of the fragile X mental retardation 1 gene.

Jenkins EC, Tassone F, Ye L, Gu H, Xi M, Velinov M, Brown WT, Hagerman RJ, Hagerman PJ. Jenkins EC, et al. Among authors: velinov m. Am J Med Genet A. 2008 Jun 15;146A(12):1543-6. doi: 10.1002/ajmg.a.32342. Am J Med Genet A. 2008. PMID: 18478592 Free PMC article.

10

Psychotic manifestations in a patient with mental retardation and a 6.2 megabase deletion at the distal short arm of chromosome 12.

Velinov M, Beldia G, Gu H, Tsiouris JA, Jenkins EC, Brown WT. Velinov M, et al. CNS Spectr. 2008 Jun;13(6):515-9. doi: 10.1017/s1092852900016758. CNS Spectr. 2008. PMID: 18567976

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