Mikhail FM - Search Results

1

Incidental detection of cancer predisposition gene copy number variations by array comparative genomic hybridization.

Hamm JA, Mikhail FM, Hollenbeck D, Farmer M, Robin NH. Hamm JA, et al. Among authors: mikhail fm. J Pediatr. 2014 Nov;165(5):1057-9.e1-4. doi: 10.1016/j.jpeds.2014.07.042. Epub 2014 Sep 4. J Pediatr. 2014. PMID: 25201531

2

Overlapping phenotype of Wolf-Hirschhorn and Beckwith-Wiedemann syndromes in a girl with der(4)t(4;11)(pter;pter).

Mikhail FM, Sathienkijkanchai A, Robin NH, Prucka S, Biggerstaff JS, Komorowski J, Andersson R, Bruder CE, Piotrowski A, Diaz de Ståhl T, Dumanski JP, Carroll AJ. Mikhail FM, et al. Am J Med Genet A. 2007 Aug 1;143A(15):1760-6. doi: 10.1002/ajmg.a.31821. Am J Med Genet A. 2007. PMID: 17603794

3

Use of array comparative genome hybridization in orofacial clefting.

Gallego CJ, Grant J, Mikhail FM, Barger C, Robin NH. Gallego CJ, et al. Among authors: mikhail fm. J Craniofac Surg. 2010 Sep;21(5):1591-4. doi: 10.1097/SCS.0b013e3181ebcc9c. J Craniofac Surg. 2010. PMID: 20856054

4

Microdeletion/microduplication of proximal 15q11.2 between BP1 and BP2: a susceptibility region for neurological dysfunction including developmental and language delay.

Burnside RD, Pasion R, Mikhail FM, Carroll AJ, Robin NH, Youngs EL, Gadi IK, Keitges E, Jaswaney VL, Papenhausen PR, Potluri VR, Risheg H, Rush B, Smith JL, Schwartz S, Tepperberg JH, Butler MG. Burnside RD, et al. Among authors: mikhail fm. Hum Genet. 2011 Oct;130(4):517-28. doi: 10.1007/s00439-011-0970-4. Epub 2011 Feb 27. Hum Genet. 2011. PMID: 21359847 Free PMC article.

5

Clinically relevant single gene or intragenic deletions encompassing critical neurodevelopmental genes in patients with developmental delay, mental retardation, and/or autism spectrum disorders.

Mikhail FM, Lose EJ, Robin NH, Descartes MD, Rutledge KD, Rutledge SL, Korf BR, Carroll AJ. Mikhail FM, et al. Am J Med Genet A. 2011 Oct;155A(10):2386-96. doi: 10.1002/ajmg.a.34177. Am J Med Genet A. 2011. PMID: 22031302

6

Transgenic mice overexpressing neuregulin-1 model neurofibroma-malignant peripheral nerve sheath tumor progression and implicate specific chromosomal copy number variations in tumorigenesis.

Kazmi SJ, Byer SJ, Eckert JM, Turk AN, Huijbregts RP, Brossier NM, Grizzle WE, Mikhail FM, Roth KA, Carroll SL. Kazmi SJ, et al. Among authors: mikhail fm. Am J Pathol. 2013 Mar;182(3):646-67. doi: 10.1016/j.ajpath.2012.11.017. Epub 2013 Jan 13. Am J Pathol. 2013. PMID: 23321323 Free PMC article.

7

The recurrent distal 22q11.2 microdeletions are often de novo and do not represent a single clinical entity: a proposed categorization system.

Mikhail FM, Burnside RD, Rush B, Ibrahim J, Godshalk R, Rutledge SL, Robin NH, Descartes MD, Carroll AJ. Mikhail FM, et al. Genet Med. 2014 Jan;16(1):92-100. doi: 10.1038/gim.2013.79. Epub 2013 Jun 13. Genet Med. 2014. PMID: 23765049 Free article.

8

Copy number variations and human genetic disease.

Mikhail FM. Mikhail FM. Curr Opin Pediatr. 2014 Dec;26(6):646-52. doi: 10.1097/MOP.0000000000000142. Curr Opin Pediatr. 2014. PMID: 25198053 Review.

9

Array comparative genomic hybridisation testing in CHD.

Hightower HB, Robin NH, Mikhail FM, Ambalavanan N. Hightower HB, et al. Among authors: mikhail fm. Cardiol Young. 2015 Aug;25(6):1155-72. doi: 10.1017/S1047951114001838. Epub 2014 Oct 8. Cardiol Young. 2015. PMID: 25296170

10

Predictor(s) of Abnormal Array Comparative Genomic Hybridization Results in Patients With Cleft Lip and/or Palate.

Rojnueangnit K, Mikhail FM, Cui X, Yu S, Robin NH. Rojnueangnit K, et al. Among authors: mikhail fm. Cleft Palate Craniofac J. 2015 Nov;52(6):724-31. doi: 10.1597/14-088. Epub 2014 Dec 9. Cleft Palate Craniofac J. 2015. PMID: 25489768

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