The leukemia-associated transcription repressor AML1/MDS1/EVI1 requires CtBP to induce abnormal growth and differentiation of murine hematopoietic cellsSENYUK, Vitalyi; CHAKRABORTY, Soumen; MIKHAIL, Fady M et al.Oncogene (Basingstoke). 2002, Vol 21, Num 20, pp 3232-3240, issn 0950-9232Article

Monosomy1p36.3 and Trisomy 19p13.3 in a Child With Periventricular Nodular HeterotopiaDESCARTES, Maria; MIKHAIL, Fady M; FRANKLIN, Judith C et al.Pediatric neurology. 2011, Vol 45, Num 4, pp 274-278, issn 0887-8994, 5 p.Article

The distal zinc finger domain of AML1/MDS1/EVI1 is an oligomerization domain involved in induction of hematopoietic differentiation defects in primary cells in vitroSENYUK, Vitalyi; DONGLAN LI; ZAKHAROV, Alexander et al.Cancer research (Baltimore). 2005, Vol 65, Num 17, pp 7603-7611, issn 0008-5472, 9 p.Article

In vivo regulation of the heme oxygenase-1 gene in humanized transgenic miceKIM, Junghyun; ZARJOU, Abolfazl; TRAYLOR, Amie M et al.Kidney international. 2012, Vol 82, Num 3, pp 278-291, issn 0085-2538, 14 p.Article

Rearrangement of CRLF2 is associated with mutation of JAK kinases, alteration of IKZF1, Hispanic/Latino ethnicity, and a poor outcome in pediatric B-progenitor acute lymphoblastic leukemiaHARVEY, Richard C; MULLIGHAN, Charles G; CARROLL, William L et al.Blood. 2010, Vol 115, Num 26, pp 5312-5321, issn 0006-4971, 10 p.Article

Overlapping phenotype of wolf-hirschhorn and beckwith-wiedemann syndromes in a girl with der(4)t(4; 1 1)(pter;pter)MIKHAIL, Fady M; SATHIENKIJKANCHAI, Achara; DUMANSKI, Jan P et al.American journal of medical genetics. Part A. 2007, Vol 143, Num 15, pp 1760-1766, issn 1552-4825, 7 p.Article

Rearrangement of CRLF2 in B-progenitor- and Down syndrome-associated acute lymphoblastic leukemiaMULLIGHAN, Charles G; COLLINS-UNDERWOOD, J. Racquel; MIKHAIL, Fady M et al.Nature genetics. 2009, Vol 41, Num 11, pp 1243-1246, issn 1061-4036, 4 p.Article

A new translocation that rearranges the AML1 gene in a patient with T-cell acute lymphoblastic leukemiaMIKHAIL, Fady M; SERRY, Kadreya A; HATEM, Nadia et al.Cancer genetics and cytogenetics. 2002, Vol 135, Num 1, pp 96-100, issn 0165-4608Article

Clinically Relevant Single Gene or Intragenic Deletions Encompassing Critical Neurodevelopmental Genes in Patients With Developmental Delay, Mental Retardation, and/or Autism Spectrum DisordersMIKHAIL, Fady M; LOSE, Edward J; ROBIN, Nathaniel H et al.American journal of medical genetics. Part A. 2011, Vol 155, Num 10, pp 2386-2396, issn 1552-4825, 11 p.Article

Microdeletion/microduplication of proximal 15q11.2 between BP1 and BP2: a susceptibility region for neurological dysfunction including developmental and language delayBURNSIDE, Rachel D; PASION, Romela; POTLURI, Venkateswara R et al.Human genetics. 2011, Vol 130, Num 4, pp 517-528, issn 0340-6717, 12 p.Article

Molecular Characterization of a Patient With an Interstitial 1q Deletion [del(1)(q24.1q25.3)] and Distinctive Skeletal AbnormalitiesDESCARTES, Maria; HAIN, Julie Zenger; CONKLIN, Michael et al.American journal of medical genetics. Part A. 2008, Vol 146, Num 22, pp 2937-2943, issn 1552-4825, 7 p.Article

Molecular Cytogenetic Characterization of Two Cases with Constitutional Distal 11q Duplication/ riplicationBURNSIDE, Rachel D; LOSE, Edward J; DOMINGUEZ, Maria G et al.American journal of medical genetics. Part A. 2009, Vol 149, Num 7, pp 1516-1522, issn 1552-4825, 7 p.Article

Distal 22qll.2 Microduplication Encompassing the BCR GeneDESCARTES, Maria; FRANKLIN, Judy; DIAZ DE STAHL, Teresita et al.American journal of medical genetics. Part A. 2008, Vol 146, Num 23, pp 3075-3081, issn 1552-4825, 7 p.Article

Complete trisomy 17p syndrome in a girl with der(14)t(14;17)(p11.2;p11.2)MIKHAIL, Fady M; MCILVRIED, Dawn; HOLT, R. Lynn et al.American journal of medical genetics. Part A. 2006, Vol 140, Num 15, pp 1647-1654, issn 1552-4825, 8 p.Article