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FAYEZ MIKHAIL, MD
MD
Internal Medicine Physician
NPI: 1770696841Individual
Specialties, Licenses & Credentials
Internal Medicine PhysicianPrimary
Internal Medicine
Code: 207R00000X
MA47865(NJ)
Research & Publications (15)
Molecular cytogenetic characterization of two cases with constitutional distal 11q duplication/triplication.
PMID 19533774·Am J Med Genet A·2009
5-case
A new syndrome with Stargardt macular degeneration, abnormalities of the corpus callosum, mental retardation, and dysmorphic features: a case report of two siblings.
PMID 19451813·Clin Dysmorphol·2009
5-case
Molecular characterization of a patient with an interstitial 1q deletion [del(1)(q24.1q25.3)] and distinctive skeletal abnormalities.
PMID 18925675·Am J Med Genet A·2008
5-case
A prenatally ascertained X;Y translocation characterized using conventional and molecular cytogenetics.
PMID 18384143·Am J Med Genet A·2008
5-case
A previously unrecognized microdeletion syndrome on chromosome 22 band q11.2 encompassing the BCR gene.
PMID 17676630·Am J Med Genet A·2007
5-case
Overlapping phenotype of Wolf-Hirschhorn and Beckwith-Wiedemann syndromes in a girl with der(4)t(4;11)(pter;pter).
PMID 17603794·Am J Med Genet A·2007
5-case
Complete trisomy 17p syndrome in a girl with der(14)t(14;17)(p11.2;p11.2).
PMID 16835929·Am J Med Genet A·2006
5-case
The distal zinc finger domain of AML1/MDS1/EVI1 is an oligomerization domain involved in induction of hematopoietic differentiation defects in primary cells in vitro.
PMID 16140925·Cancer Res·2005
7-preclinical
EVI1 abrogates interferon-alpha response by selectively blocking PML induction.
PMID 15519999·J Biol Chem·2005
7-preclinical
A novel gene, FGA7, is fused to RUNX1/AML1 in a t(4;21)(q28;q22) in a patient with T-cell acute lymphoblastic leukemia.
PMID 14695990·Genes Chromosomes Cancer·2004
7-preclinical
The leukemia-associated transcription repressor AML1/MDS1/EVI1 requires CtBP to induce abnormal growth and differentiation of murine hematopoietic cells.
PMID 12082639·Oncogene·2002
7-preclinical
A new translocation that rearranges the AML1 gene in a patient with T-cell acute lymphoblastic leukemia.
PMID 12072207·Cancer Genet Cytogenet·2002
5-case
AML1 gene over-expression in childhood acute lymphoblastic leukemia.
PMID 11960347·Leukemia·2002
8-other
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 23 MAYFAIR RD
SOUTHAMPTON, NJ 08088 - Phone
- (609) 587-1001
Quick Facts
- NPI
- 1770696841
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 15
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