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FREDERICK RAYMOND, MD
MD
Ophthalmology Physician
NPI: 1346205655Individual
Specialties, Licenses & Credentials
Ophthalmology PhysicianPrimary
Ophthalmology
Code: 207W00000X
G32652(CA)
Research & Publications (20)
Comparison of automated microarray detection with real-time PCR assays for detection of respiratory viruses in specimens obtained from children.
PMID 19158263·J Clin Microbiol·2009
4-observational
Lessons learnt from large-scale exon re-sequencing of the X chromosome.
PMID 19297402·Hum Mol Genet·2009
6-review
Mutations in ZDHHC9, which encodes a palmitoyltransferase of NRAS and HRAS, cause X-linked mental retardation associated with a Marfanoid habitus.
PMID 17436253·Am J Hum Genet·2007
5-case
Quantification of homozygosity in consanguineous individuals with autosomal recessive disease.
PMID 16642444·Am J Hum Genet·2006
8-other
Detection of target DNA using fluorescent cationic polymer and peptide nucleic acid probes on solid support.
PMID 15850478·BMC Biotechnol·2005
8-other
Genetic services for people with intellectual disability and their families.
PMID 12974883·J Intellect Disabil Res·2003
8-other
Measurement and interpretation of hand hygiene compliance rates: importance of monitoring entire care episodes.
PMID 19481837·J Hosp Infect·2009
8-other
Bone scintigraphy in femoroacetabular impingement: a preliminary report.
PMID 19089523·Clin Orthop Relat Res·2009
8-other
Gene expression modulation is associated with gene amplification, supernumerary chromosomes and chromosome loss in antimony-resistant Leishmania infantum.
PMID 19129236·Nucleic Acids Res·2009
7-preclinical
A systematic, large-scale resequencing screen of X-chromosome coding exons in mental retardation.
PMID 19377476·Nat Genet·2009
8-other
Whole-genome comparative RNA expression profiling of axenic and intracellular amastigote forms of Leishmania infantum.
PMID 19393160·Mol Biochem Parasitol·2009
4-observational
Modulation of gene expression in drug resistant Leishmania is associated with gene amplification, gene deletion and chromosome aneuploidy.
PMID 18638379·Genome Biol·2008
7-preclinical
SLC9A6 mutations cause X-linked mental retardation, microcephaly, epilepsy, and ataxia, a phenotype mimicking Angelman syndrome.
PMID 18342287·Am J Hum Genet·2008
8-other
Phenotypical characteristics of idiopathic infantile nystagmus with and without mutations in FRMD7.
PMID 18372314·Brain·2008
4-observational
Genome-wide gene expression profiling analysis of Leishmania major and Leishmania infantum developmental stages reveals substantial differences between the two species.
PMID 18510761·BMC Genomics·2008
4-observational
Murine intestinal cells expressing Trpm5 are mostly brush cells and express markers of neuronal and inflammatory cells.
PMID 18537122·J Comp Neurol·2008
4-observational
Donnai-Barrow syndrome (DBS/FOAR) in a child with a homozygous LRP2 mutation due to complete chromosome 2 paternal isodisomy.
PMID 18553518·Am J Med Genet A·2008
5-case
Genetic research on rare familial disorders: consent and the blurred boundaries between clinical service and research.
PMID 18757643·J Med Ethics·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
- 7247 SO PAINTER AVENUE
WHITTIER, CA 90602 - Phone
- (562) 945-3589
Quick Facts
- NPI
- 1346205655
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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