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MEGHAN IRONS, PHARMD

PHARMD

Pharmacist

NPI: 1497028583Individual

Specialties, Licenses & Credentials

PharmacistPrimary

Pharmacist

Code: 183500000X

PH60235917(WA)

Research & Publications (20)

Mutations in the gene encoding the calcium-permeable ion channel TRPV4 produce spondylometaphyseal dysplasia, Kozlowski type and metatropic dysplasia.
PMID 19232556·Am J Hum Genet·2009
8-other
ACMG practice guideline: genetic evaluation of short stature.
PMID 19451827·Genet Med·2009
6-review
The genetics clinic: where does the time go?
PMID 18978676·Genet Med·2008
8-other
Development of a focused oligonucleotide-array comparative genomic hybridization chip for clinical diagnosis of genomic imbalance.
PMID 17901113·Clin Chem·2007
4-observational
The spectrum of vascular anomalies in patients with PTEN mutations: implications for diagnosis and management.
PMID 17526801·J Med Genet·2007
8-other
A newly recognized craniosynostosis syndrome with features of Aarskog-Scott and Teebi syndromes.
PMID 17506099·Am J Med Genet A·2007
8-other
Brainstem lesions in neurofibromatosis type 1.
PMID 17986937·Neurosurgery·2007
4-observational
Diagnostic utility of array-based comparative genomic hybridization in a clinical setting.
PMID 17910064·Am J Med Genet A·2007
4-observational
Increased MECP2 gene copy number as the result of genomic duplication in neurodevelopmentally delayed males.
PMID 17172942·Genet Med·2006
5-case
Patient with novel interstitial deletion of chromosome 3q13.1q13.3 and agenesis of the corpus callosum.
PMID 16957476·Clin Dysmorphol·2006
5-case
Identification of a novel polymorphism--the duplication of the NPHP1 (nephronophthisis 1) gene.
PMID 16892302·Am J Med Genet A·2006
5-case
Identifying Smith-Lemli-Opitz syndrome in conjunction with prenatal screening for Down syndrome.
PMID 16832833·Prenat Diagn·2006
4-observational
Smith-Lemli-Opitz syndrome in trisomy 13: how does the mix work?
PMID 15965973·Birth Defects Res A Clin Mol Teratol·2005
5-case
Construction of a natural panel of 11p11.2 deletions and further delineation of the critical region involved in Potocki-Shaffer syndrome.
PMID 15852040·Eur J Hum Genet·2005
5-case
Fryns syndrome with Hirschsprung disease: support for possible neural crest involvement.
PMID 15580636·Am J Med Genet A·2005
5-case
Subtelomeric deletions of chromosome 9q: a novel microdeletion syndrome.
PMID 15264279·Am J Med Genet A·2004
8-other
MRI and 1H MRS findings in Smith-Lemli-Opitz syndrome.
PMID 14605787·Neuroradiology·2004
8-other
The call from the newborn screening laboratory: frustration in the afternoon.
PMID 15157599·Pediatr Clin North Am·2004
6-review
Clinical presentation of 13 patients with subtelomeric rearrangements and a review of the literature.
PMID 15264280·Am J Med Genet A·2004
5-case
Description of a case of distal 2p trisomy by array-based comparative genomic hybridization: a high resolution genome-wide investigation for chromosomal aneuploidy in a single assay.
PMID 15372522·Am J Med Genet A·2004
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
1651 W ROSE ST
WALLA WALLA, WA 99362

Location

Practice Location

1651 W ROSE ST, WALLA WALLA, WA
(509) 525-9207

Quick Facts

NPI
1497028583
Entity Type
Individual
Gender
Female
Medicare
Not confirmed
Specialties
1
Locations
1
Publications
20

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