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SARITHA VERMEER, PH.D.
PH.D.
Clinical Psychologist
NPI: 1699907519Individual
Specialties, Licenses & Credentials
Research & Publications (20)
Refining the critical region of the novel 19q13.11 microdeletion syndrome to 750 Kb.
PMID 19487540·J Med Genet·2009
8-other
GJA1 mutations, variants, and connexin 43 dysfunction as it relates to the oculodentodigital dysplasia phenotype.
PMID 19338053·Hum Mutat·2009
6-review
Comprehensive clinical and molecular assessment of 32 probands with congenital contractural arachnodactyly: report of 14 novel mutations and review of the literature.
PMID 19006240·Hum Mutat·2009
6-review
Efficient amplification with NASBA of hepatitis B virus, herpes simplex virus and methicillin resistant Staphylococcus aureus DNA.
PMID 18514336·J Virol Methods·2008
8-other
ARSACS in the Dutch population: a frequent cause of early-onset cerebellar ataxia.
PMID 18465152·Neurogenetics·2008
8-other
Mutation analysis of CHRNA1, CHRNB1, CHRND, and RAPSN genes in multiple pterygium syndrome/fetal akinesia patients.
PMID 18179903·Am J Hum Genet·2008
8-other
Cerebellar ataxia and congenital disorder of glycosylation Ia (CDG-Ia) with normal routine CDG screening.
PMID 17694350·J Neurol·2007
5-case
A novel microdeletion in 1(p34.2p34.3), involving the SLC2A1 (GLUT1) gene, and severe delayed development.
PMID 17489814·Dev Med Child Neurol·2007
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
- 4020 N ROXBORO ST
DURHAM, NC 27704 - Phone
- (919) 684-8111
Quick Facts
- NPI
- 1699907519
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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