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DAVID STEINBERGER, PHD
PHD
Psychologist
NPI: 1396812913Individual
Specialties, Licenses & Credentials
PsychologistPrimary
Psychologist
Code: 103T00000X
PSY6192(CA)
Research & Publications (17)
A monoallelic double mutation as a cause for TNF receptor-associated periodic fever syndrome.
PMID 19547977·Rheumatol Int·2010
5-case
Enhancer deletions of the SHOX gene as a frequent cause of short stature: the essential role of a 250 kb downstream regulatory domain.
PMID 19578035·J Med Genet·2009
8-other
Hypergonadotropic hypogonadism in a patient with inv ins (2;4).
PMID 18042180·Int J Androl·2009
5-case
Frequency of GCH1 deletions in Dopa-responsive dystonia.
PMID 17898029·J Neurol Neurosurg Psychiatry·2008
8-other
Utility of MLPA in deletion analysis of GCH1 in dopa-responsive dystonia.
PMID 17111153·Neurogenetics·2007
8-other
Mutation screening for the prothrombin variant G20210A by melting point analysis with the Light Cycler system: atypical results, detection of the variant C20209T and possible clinical implications.
PMID 16178919·Clin Lab Haematol·2005
5-case
Heterozygous mutation in 5'-untranslated region of sepiapterin reductase gene (SPR) in a patient with dopa-responsive dystonia.
PMID 15241655·Neurogenetics·2004
8-other
Molecular analysis of patients with synostotic frontal plagiocephaly (unilateral coronal synostosis).
PMID 15253176·Plast Reconstr Surg·2004
8-other
Development of the University of Wisconsin donation After Cardiac Death Evaluation Tool.
PMID 14765718·Prog Transplant·2003
4-observational
Genetic mapping of variation in spatial learning in the mouse.
PMID 12657702·J Neurosci·2003
7-preclinical
Standardized evaluation and documentation of findings in patients with craniosynostosis.
PMID 11467491·J Craniomaxillofac Surg·2001
4-observational
Standardized evaluation and documentation of findings in patients with craniosynostosis.
PMID 11308276·J Maxillofac Surg·2001
8-other
Dopa-responsive dystonia: mutation analysis of GCH1 and analysis of therapeutic doses of L-dopa. German Dystonia Study Group.
PMID 11113234·Neurology·2000
8-other
Prominent basal emissary foramina in syndromic craniosynostosis: correlation with phenotypic and molecular diagnoses.
PMID 11039354·AJNR Am J Neuroradiol·2000
8-other
Features of Antley-Bixler syndrome in an infant born to a mother with pregnancy luteoma.
PMID 10664233·Eur J Pediatr·2000
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
- 12530 10TH STREET, SUITE C
CHINO, CA 91710 - Phone
- (909) 591-4264
Quick Facts
- NPI
- 1396812913
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 17
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