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FELICITAS LACBAWAN, M.D.
M.D.
Molecular Genetic Pathology (Pathology) Physician
NPI: 1518045822Individual
Specialties, Licenses & Credentials
Molecular Genetic Pathology (Pathology) PhysicianPrimary
Pathology — Molecular Genetic Pathology
Code: 207ZP0007X
35098505(OH)253903-1(NY)
Anatomic Pathology & Clinical Pathology Physician
Pathology — Anatomic Pathology & Clinical Pathology
Code: 207ZP0102X
253903-1(NY)
Clinical Genetics (M.D.) Physician
Medical Genetics — Clinical Genetics (M.D.)
Code: 207SG0201X
253903-1(NY)
Research & Publications (20)
The mutational spectrum of holoprosencephaly-associated changes within the SHH gene in humans predicts loss-of-function through either key structural alterations of the ligand or its altered synthesis.
PMID 19603532·Hum Mutat·2009
8-other
A novel SIX3 mutation segregates with holoprosencephaly in a large family.
PMID 19353631·Am J Med Genet A·2009
8-other
Clinical spectrum of SIX3-associated mutations in holoprosencephaly: correlation between genotype, phenotype and function.
PMID 19346217·J Med Genet·2009
8-other
Truncating loss-of-function mutations of DISP1 contribute to holoprosencephaly-like microform features in humans.
PMID 19184110·Hum Genet·2009
7-preclinical
The full spectrum of holoprosencephaly-associated mutations within the ZIC2 gene in humans predicts loss-of-function as the predominant disease mechanism.
PMID 19177455·Hum Mutat·2009
8-other
Mutations in the human SIX3 gene in holoprosencephaly are loss of function.
PMID 18791198·Hum Mol Genet·2008
4-observational
Brain-derived neurotrophic factor and obesity in the WAGR syndrome.
PMID 18753648·N Engl J Med·2008
8-other
Reduced NODAL signaling strength via mutation of several pathway members including FOXH1 is linked to human heart defects and holoprosencephaly.
PMID 18538293·Am J Hum Genet·2008
7-preclinical
Muenke syndrome (FGFR3-related craniosynostosis): expansion of the phenotype and review of the literature.
PMID 18000976·Am J Med Genet A·2007
8-other
Abnormal sterol metabolism in holoprosencephaly: studies in cultured lymphoblasts.
PMID 17237122·J Med Genet·2007
8-other
Functional analysis of mutations in TGIF associated with holoprosencephaly.
PMID 16962354·Mol Genet Metab·2007
5-case
Multicolour FISH and quantitative PCR can detect submicroscopic deletions in holoprosencephaly patients with a normal karyotype.
PMID 16199538·J Med Genet·2006
8-other
A female infant with duplication of chromosome 2q33 to 2q37.3.
PMID 14564213·Clin Dysmorphol·2003
5-case
Large interstitial deletion of chromosome 13q and severe short stature: clinical report and review of the literature.
PMID 14564160·Clin Dysmorphol·2003
5-case
Report of a child with aortic aneurysm, orofacial clefting, hemangioma, upper sternal defect, and marfanoid features: possible PHACE syndrome.
PMID 12116239·Am J Med Genet·2002
5-case
Association between conformational mutations in neuroserpin and onset and severity of dementia.
PMID 12103288·Lancet·2002
8-other
Clinical heterogeneity in mitochondrial DNA deletion disorders: a diagnostic challenge of Pearson syndrome.
PMID 11102933·Am J Med Genet·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
- Address
- 9500 EUCLID AVE, CLEVELAND CLINIC MOLECULAR PATHOLOGY MC:LL2-2
CLEVELAND, OH 44195 - Phone
- (216) 445-0761
Quick Facts
- NPI
- 1518045822
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 4
- Locations
- 1
- Publications
- 20
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