Mikhail FM - Search Results

1

Constitutional balanced translocations involving SMARCB1: A rare cause of rhabdoid tumor predisposition syndrome.

Blackburn PR, McGee RB, Mostafavi R, Carroll AJ, Mikhail FM, Armstrong GT, Furtado LV, Chiang J, Wheeler DA, Carey SS, Nichols KE, Upadhyaya SA. Blackburn PR, et al. Among authors: mikhail fm. Genes Chromosomes Cancer. 2024 Jan;63(1):e23195. doi: 10.1002/gcc.23195. Epub 2023 Aug 7. Genes Chromosomes Cancer. 2024. PMID: 37548271

2

A case of acute promyelocytic leukemia without RARα rearrangement and apparently normal cytogenetics.

Vaklavas C, Steciuk MR, Ren Y, Baird MF, Mikhail FM, Foran JM. Vaklavas C, et al. Among authors: mikhail fm. Clin Lymphoma Myeloma Leuk. 2011 Dec;11(6):521-4. doi: 10.1016/j.clml.2011.03.036. Epub 2011 May 19. Clin Lymphoma Myeloma Leuk. 2011. PMID: 21729689 No abstract available.

3

AML1 gene over-expression in childhood acute lymphoblastic leukemia.

Mikhail FM, Serry KA, Hatem N, Mourad ZI, Farawela HM, El Kaffash DM, Coignet L, Nucifora G. Mikhail FM, et al. Leukemia. 2002 Apr;16(4):658-68. doi: 10.1038/sj.leu.2402399. Leukemia. 2002. PMID: 11960347

4

The leukemia-associated transcription repressor AML1/MDS1/EVI1 requires CtBP to induce abnormal growth and differentiation of murine hematopoietic cells.

Senyuk V, Chakraborty S, Mikhail FM, Zhao R, Chi Y, Nucifora G. Senyuk V, et al. Among authors: mikhail fm. Oncogene. 2002 May 9;21(20):3232-40. doi: 10.1038/sj.onc.1205436. Oncogene. 2002. PMID: 12082639

5

Complete trisomy 17p syndrome in a girl with der(14)t(14;17)(p11.2;p11.2).

Mikhail FM, McIlvried D, Holt RL, Messiaen L, Descartes MD, Carroll AJ. Mikhail FM, et al. Am J Med Genet A. 2006 Aug 1;140(15):1647-54. doi: 10.1002/ajmg.a.31330. Am J Med Genet A. 2006. PMID: 16835929

6

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

7

A previously unrecognized microdeletion syndrome on chromosome 22 band q11.2 encompassing the BCR gene.

Mikhail FM, Descartes M, Piotrowski A, Andersson R, Diaz de Ståhl T, Komorowski J, Bruder CE, Dumanski JP, Carroll AJ. Mikhail FM, et al. Am J Med Genet A. 2007 Sep 15;143A(18):2178-84. doi: 10.1002/ajmg.a.31882. Am J Med Genet A. 2007. PMID: 17676630

8

Distal 22q11.2 microduplication encompassing the BCR gene.

Descartes M, Franklin J, Diaz de Ståhl T, Piotrowski A, Bruder CE, Dumanski JP, Carroll AJ, Mikhail FM. Descartes M, et al. Among authors: mikhail fm. Am J Med Genet A. 2008 Dec 1;146A(23):3075-81. doi: 10.1002/ajmg.a.32572. Am J Med Genet A. 2008. PMID: 19006218

9

Molecular cytogenetic characterization of two cases with constitutional distal 11q duplication/triplication.

Burnside RD, Lose EJ, Domínguez MG, Sánchez-Corona J, Rivera H, Carroll AJ, Mikhail FM. Burnside RD, et al. Among authors: mikhail fm. Am J Med Genet A. 2009 Jul;149A(7):1516-22. doi: 10.1002/ajmg.a.32906. Am J Med Genet A. 2009. PMID: 19533774

10

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

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