Hovanes K - Search Results

1

A novel familial 11p15.4 microduplication associated with intellectual disability, dysmorphic features, and obesity with involvement of the ZNF214 gene.

Sofos E, Pescosolido MF, Quintos JB, Abuelo D, Gunn S, Hovanes K, Morrow EM, Shur N. Sofos E, et al. Among authors: hovanes k. Am J Med Genet A. 2012 Jan;158A(1):50-8. doi: 10.1002/ajmg.a.34290. Epub 2011 Nov 3. Am J Med Genet A. 2012. PMID: 22052655

2

Inversion and deletion of 16q22 defined by array CGH, FISH, and RT-PCR in a patient with AML.

Dawson AJ, Bal S, McTavish B, Tomiuk M, Schroedter I, Ahsanuddin AN, Seftel MD, Vallente R, Mai S, Cotter PD, Hovanes K, Gorre M, Gunn SR. Dawson AJ, et al. Among authors: hovanes k. Cancer Genet. 2011 Jun;204(6):344-7. doi: 10.1016/j.cancergen.2011.05.005. Cancer Genet. 2011. PMID: 21763633

3

The 3q29 microdeletion syndrome: report of three new unrelated patients and in silico "RNA binding" analysis of the 3q29 region.

Dasouki MJ, Lushington GH, Hovanes K, Casey J, Gorre M. Dasouki MJ, et al. Among authors: hovanes k. Am J Med Genet A. 2011 Jul;155A(7):1654-60. doi: 10.1002/ajmg.a.34080. Epub 2011 May 27. Am J Med Genet A. 2011. PMID: 21626679 Free PMC article.

4

Confirmation and further delineation of the 3q26.33-3q27.2 microdeletion syndrome.

Dasouki M, Roberts J, Santiago A, Saadi I, Hovanes K. Dasouki M, et al. Among authors: hovanes k. Eur J Med Genet. 2014 Feb;57(2-3):76-80. doi: 10.1016/j.ejmg.2013.12.007. Epub 2014 Jan 22. Eur J Med Genet. 2014. PMID: 24462885

5

Maternal 21-hydroxylase deficiency and uniparental isodisomy of chromosome 6 and X results in a child with 21-hydroxylase deficiency and Klinefelter syndrome.

Parker EA, Hovanes K, Germak J, Porter F, Merke DP. Parker EA, et al. Among authors: hovanes k. Am J Med Genet A. 2006 Oct 15;140(20):2236-40. doi: 10.1002/ajmg.a.31408. Am J Med Genet A. 2006. PMID: 16906568 No abstract available.

6

Comprehensive genetic analysis of pregnancy loss by chromosomal microarrays: outcomes, benefits, and challenges.

Sahoo T, Dzidic N, Strecker MN, Commander S, Travis MK, Doherty C, Tyson RW, Mendoza AE, Stephenson M, Dise CA, Benito CW, Ziadie MS, Hovanes K. Sahoo T, et al. Among authors: hovanes k. Genet Med. 2017 Jan;19(1):83-89. doi: 10.1038/gim.2016.69. Epub 2016 Jun 23. Genet Med. 2017. PMID: 27337029 Free article.

7

PWS/AS MS-MLPA Confirms Maternal Origin of 15q11.2 Microduplication.

Dawson AJ, Cox J, Hovanes K, Spriggs E. Dawson AJ, et al. Among authors: hovanes k. Case Rep Genet. 2015;2015:474097. doi: 10.1155/2015/474097. Epub 2015 May 7. Case Rep Genet. 2015. PMID: 26064710 Free PMC article.

8

Chromosome microarray and undiagnosed seizures in a pediatric patient.

Dawson AJ, Mhanni AA, Booth FA, Seargeant L, Bernier D, Tomiuk M, Hartley JN, Strecker M, Hovanes K. Dawson AJ, et al. Among authors: hovanes k. Can J Neurol Sci. 2014 Mar;41(2):281-3. doi: 10.1017/s0317167100016747. Can J Neurol Sci. 2014. PMID: 24534047 No abstract available.

9

Heterozygous intragenic deletions of FREM1 are not associated with trigonocephaly.

Dawson AJ, Hovanes K, Liu J, Marles S, Greenberg C, Mhanni A, Chudley A, Frosk P, Sahoo T, Schanze D, Zenker M. Dawson AJ, et al. Among authors: hovanes k. Clin Dysmorphol. 2021 Apr 1;30(2):83-88. doi: 10.1097/MCD.0000000000000351. Clin Dysmorphol. 2021. PMID: 33038106

10

Structural Chromosome Abnormalities Associated with Obesity: Report of Four New subjects and Review of Literature.

Dasouki MJ, Youngs EL, Hovanes K. Dasouki MJ, et al. Among authors: hovanes k. Curr Genomics. 2011 May;12(3):190-203. doi: 10.2174/138920211795677930. Curr Genomics. 2011. PMID: 22043167 Free PMC article.

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