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KENNETH ROSENBAUM, MD
MD
Pediatrics Physician
NPI: 1407922404Individual
Specialties, Licenses & Credentials
Pediatrics PhysicianPrimary
Pediatrics
Code: 208000000X
G76294(CA)
Research & Publications (10)
Clinical and molecular analysis of arylsulfatase E in patients with brachytelephalangic chondrodysplasia punctata.
PMID 18348268·Am J Med Genet A·2008
8-other
Muenke syndrome (FGFR3-related craniosynostosis): expansion of the phenotype and review of the literature.
PMID 18000976·Am J Med Genet A·2007
8-other
Prolyl 3-hydroxylase 1 deficiency causes a recessive metabolic bone disorder resembling lethal/severe osteogenesis imperfecta.
PMID 17277775·Nat Genet·2007
5-case
[Factors influencing corneal endothelium in organ cultures during transport].
PMID 15197572·Ophthalmologe·2004
4-observational
Scanning for telomeric deletions and duplications and uniparental disomy using genetic markers in 120 children with malformations.
PMID 11702212·Hum Genet·2001
8-other
On the iron-sulfur clusters in the complex redox enzyme dihydropyrimidine dehydrogenase.
PMID 10848981·Eur J Biochem·2000
8-other
Exclusion of the branchio-oto-renal syndrome locus (EYA1) from patients with branchio-oculo-facial syndrome.
PMID 10767004·Am J Med Genet·2000
8-other
Neurodevelopmental and neuroimaging correlates in nonsyndromal microcephalic children.
PMID 10706344·J Dev Behav Pediatr·2000
8-other
Detection of chromosomal aberrations by a whole-genome microsatellite screen.
PMID 10677301·Am J Hum Genet·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
- 123 S SAN MATEO DR
SAN MATEO, CA 94401 - Phone
- (650) 343-4200
Quick Facts
- NPI
- 1407922404
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 10
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