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PAUL OTTO, PHARM.D.
PHARM.D.
Pharmacist
NPI: 1407850399Individual
Specialties, Licenses & Credentials
PharmacistPrimary
Pharmacist
Code: 183500000X
P5603(ID)
Research & Publications (20)
Heterozygosity probabilities for normal relatives of isolated cases affected by incompletely penetrant conditions and the calculation of recurrence risks for their offspring. I. Autosomal dominant genes.
PMID 11074493·Am J Med Genet·2000
8-other
Evidence of interspecies transmission and reassortment among avian group A rotaviruses.
PMID 19249805·Virology·2009
4-observational
Constitutional haploinsufficiency of tumor suppressor genes in mentally retarded patients with microdeletions in 17p13.1.
PMID 19617690·Cytogenet Genome Res·2009
5-case
A novel autosomal dominant deafness locus (DFNA58) maps to 2p12-p21.
PMID 19159392·Clin Genet·2009
8-other
The first complete genome sequence of a chicken group A rotavirus indicates independent evolution of mammalian and avian strains.
PMID 19246068·Virology·2009
4-observational
Abdominal pain in a patient with ankylosing spondylitis under treatment with infliximab.
PMID 19590442·J Clin Rheumatol·2009
5-case
Prevalence of GJB2 (connexin-26) and GJB6 (connexin-30) mutations in a cohort of 300 Brazilian hearing-impaired individuals: implications for diagnosis and genetic counseling.
PMID 19125024·Ear Hear·2009
8-other
HTR1B and HTR2C in autism spectrum disorders in Brazilian families.
PMID 19038234·Brain Res·2009
8-other
Novel mutations in IRF6 in nonsyndromic cleft lip with or without cleft palate: when should IRF6 mutational screening be done?
PMID 19449419·Am J Med Genet A·2009
8-other
Spastic paraplegia, optic atrophy, and neuropathy: new observations, locus refinement, and exclusion of candidate genes.
PMID 19344448·Ann Hum Genet·2009
8-other
HaloTag: a novel protein labeling technology for cell imaging and protein analysis.
PMID 18533659·ACS Chem Biol·2008
7-preclinical
A novel locus for split-hand/foot malformation associated with tibial hemimelia (SHFLD syndrome) maps to chromosome region 17p13.1-17p13.3.
PMID 18493797·Hum Genet·2008
5-case
A previously undescribed syndrome combining fibular agenesis/hypoplasia, oligodactylous clubfeet, anonychia/ungual hypoplasia, and other defects.
PMID 19012338·Am J Med Genet A·2008
5-case
Chromosome abnormalities in two patients with features of autosomal dominant Robinow syndrome.
PMID 17603805·Am J Med Genet A·2007
5-case
Clinical characterization of autosomal dominant and recessive variants of Robinow syndrome.
PMID 17256787·Am J Med Genet A·2007
8-other
Detection of Francisella tularensis subsp. holarctica in a European brown hare (Lepus europaeus) in Thuringia, Germany.
PMID 17482385·Vet Microbiol·2007
5-case
Serotype 1 and 2 bovine noroviruses are endemic in cattle in the United kingdom and Germany.
PMID 17596356·J Clin Microbiol·2007
7-preclinical
Detection of rotaviruses and intestinal lesions in broiler chicks from flocks with runting and stunting syndrome (RSS).
PMID 17039842·Avian Dis·2006
7-preclinical
Whole-genome array-CGH screening in undiagnosed syndromic patients: old syndromes revisited and new alterations.
PMID 17124408·Cytogenet Genome Res·2006
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
- 444 HOSPITAL WAY, SUITE 801
POCATELLO, ID 83201 - Phone
- (208) 232-6214
Quick Facts
- NPI
- 1407850399
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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