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MAJED DASOUKI, MD
MD
Clinical Genetics (M.D.) Physician
NPI: 1568454981IndividualAccepts Medicare
Specialties, Licenses & Credentials
Clinical Cytogenetics Physician
Medical Genetics — Clinical Cytogenetics
Code: 207SC0300X
ME145275(FL)
Clinical Biochemical Genetics Physician
Medical Genetics — Clinical Biochemical Genetics
Code: 207SG0202X
ME145275(FL)
Pediatrics Physician
Pediatrics
Code: 208000000X
117706(MO)
Clinical Genetics (M.D.) PhysicianPrimary
Medical Genetics — Clinical Genetics (M.D.)
Code: 207SG0201X
ME145275(FL)
CMS Specialties
PrimaryMEDICAL GENETICS AND GENOMICS
Additional
PEDIATRIC MEDICINE
Education
OTHER
Class of 1982
Research & Publications (15)
Compound heterozygous mutations in fibulin-4 causing neonatal lethal pulmonary artery occlusion, aortic aneurysm, arachnodactyly, and mild cutis laxa.
PMID 17937443·Am J Med Genet A·2007
5-case
Expanded newborn screening of inherited metabolic disorders by tandem mass spectrometry: clinical and laboratory aspects.
PMID 16563365·Clin Biochem·2006
6-review
A 9-year-old male with a duplication of chromosome 3p25.3p26.2: clinical report and gene expression analysis.
PMID 16470700·Am J Med Genet A·2006
5-case
Functional analysis of NBC1 mutants associated with proximal renal tubular acidosis and ocular abnormalities.
PMID 15930088·J Am Soc Nephrol·2005
7-preclinical
Subset of individuals with autism spectrum disorders and extreme macrocephaly associated with germline PTEN tumour suppressor gene mutations.
PMID 15805158·J Med Genet·2005
5-case
Germline PTEN promoter mutations and deletions in Cowden/Bannayan-Riley-Ruvalcaba syndrome result in aberrant PTEN protein and dysregulation of the phosphoinositol-3-kinase/Akt pathway.
PMID 12844284·Am J Hum Genet·2003
8-other
Coenzyme Q10 levels in Prader-Willi syndrome: comparison with obese and non-obese subjects.
PMID 12749057·Am J Med Genet A·2003
4-observational
Childhood hyperuricemia and acute renal failure resulting from a missense mutation in the HPRT gene.
PMID 11891689·Am J Med Genet·2002
5-case
A 9-month-old baby with subdural hematomas, retinal hemorrhages, and developmental delay.
PMID 11862140·Pediatr Emerg Care·2002
5-case
Role of common gene variations in the molecular pathogenesis of short-chain acyl-CoA dehydrogenase deficiency.
PMID 11134486·Pediatr Res·2001
8-other
Identification of a novel mutation in patients with medium-chain acyl-CoA dehydrogenase deficiency.
PMID 10767181·Mol Genet Metab·2000
5-case
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
Via practice · 2 locations total
- Address
- 4620 J C NICHOLS PKWY, SUITE 405
KANSAS CITY, MO 64112 - Phone
- (816) 960-0300
Quick Facts
- NPI
- 1568454981
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Accepted
- Specialties
- 4
- Locations
- 2
- Years in Practice
- 44
- Publications
- 15
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