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BASSEM BEJJANI, M.D.
M.D.
Ph.D. Medical Genetics
NPI: 1851349625Individual
Specialties, Licenses & Credentials
Ph.D. Medical GeneticsPrimary
Medical Genetics, Ph.D. Medical Genetics
Code: 170100000X
MTS 4427(WA)
Research & Publications (20)
Clinical utility of contemporary molecular cytogenetics.
PMID 18949852·Annu Rev Genomics Hum Genet·2008
6-review
Application of array-based comparative genomic hybridization to clinical diagnostics.
PMID 17065418·J Mol Diagn·2006
6-review
Use of targeted array-based CGH for the clinical diagnosis of chromosomal imbalance: is less more?
PMID 15723295·Am J Med Genet A·2005
4-observational
Array-based comparative genomic hybridization in clinical diagnosis.
PMID 15934818·Expert Rev Mol Diagn·2005
4-observational
Impact of genotype-first diagnosis: the detection of microdeletion and microduplication syndromes with cancer predisposition by aCGH.
PMID 19365269·Genet Med·2009
8-other
Contrasting changes in cortical activation induced by acute high-frequency stimulation within the globus pallidus in Parkinson's disease.
PMID 18781162·J Cereb Blood Flow Metab·2009
3-trial
Localization of a gene for keratoconus to a 5.6-Mb interval on 13q32.
PMID 19011015·Invest Ophthalmol Vis Sci·2009
8-other
Genomic and genic deletions of the FOX gene cluster on 16q24.1 and inactivating mutations of FOXF1 cause alveolar capillary dysplasia and other malformations.
PMID 19500772·Am J Hum Genet·2009
8-other
Identification of a rare de novo three-way complex t(5;20;8)(q31;p11.2;p21) with microdeletions on 5q31.2, 5q31.3, and 8p23.2 in a patient with hearing loss and global developmental delay: case report.
PMID 19128483·Mol Cytogenet·2009
8-other
Identification of familial and de novo microduplications of 22q11.21-q11.23 distal to the 22q11.21 microdeletion syndrome region.
PMID 19193630·Hum Mol Genet·2009
8-other
aCGH detects partial tetrasomy of 12p in blood from Pallister-Killian syndrome cases without invasive skin biopsy.
PMID 19353629·Am J Med Genet A·2009
8-other
Williams syndrome in a preterm infant with phenotype of Alagille syndrome.
PMID 18688871·Am J Med Genet A·2008
5-case
Identification of a previously unrecognized microdeletion syndrome of 16q11.2q12.2.
PMID 18811697·Clin Genet·2008
5-case
The variability of levodopa response in Parkinson's disease: is sensitization reversible?
PMID 18163452·Mov Disord·2008
8-other
Does dopamine still have a leading role in advanced Parkinson's disease after subthalamic stimulation?
PMID 18421247·Stereotact Funct Neurosurg·2008
5-case
Expanding the clinical phenotype of the 3q29 microdeletion syndrome and characterization of the reciprocal microduplication.
PMID 18471269·Mol Cytogenet·2008
8-other
Comparison of microarray-based detection rates for cytogenetic abnormalities in prenatal and neonatal specimens.
PMID 18646242·Prenat Diagn·2008
4-observational
Array comparative genomic hybridization in global developmental delay.
PMID 18361433·Am J Med Genet B Neuropsychiatr Genet·2008
8-other
An instructive case of an 8-year-old boy with intellectual disability.
PMID 19073314·Semin Pediatr Neurol·2008
5-case
Human anterior chamber angle development without cell death or macrophage involvement.
PMID 19112535·Mol Vis·2008
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
- 44 W 6TH AVE, SUITE 202
SPOKANE, WA 99204 - Phone
- (509) 474-6840
Quick Facts
- NPI
- 1851349625
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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