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MICHELE IRONS, MD

MD

Internal Medicine Physician

NPI: 1366402141Individual

Specialties, Licenses & Credentials

Internal Medicine PhysicianPrimary

Internal Medicine

Code: 207R00000X

0101239548(VA)

CMS Specialties

PrimaryINTERNAL MEDICINE

Education

DREXEL UNIVERSITY COLLEGE OF MEDICINE

Class of 2003

Research & Publications (20)

The genetics clinic: where does the time go?
PMID 18978676·Genet Med·2008
8-other
Cholesterol in childhood: friend or foe?: Commentary on the article by Merkens et al. on page 726.
PMID 15496612·Pediatr Res·2004
6-review
Use of subtelomeric fluorescence in situ hybridization in cytogenetic diagnosis.
PMID 14631205·Curr Opin Pediatr·2003
6-review
Mental status screening of emergency department patients: normative study of the quick confusion scale.
PMID 12359535·Acad Emerg Med·2002
3-trial
ACMG practice guideline: genetic evaluation of short stature.
PMID 19451827·Genet Med·2009
6-review
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
The spectrum of vascular anomalies in patients with PTEN mutations: implications for diagnosis and management.
PMID 17526801·J Med Genet·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
Development of a focused oligonucleotide-array comparative genomic hybridization chip for clinical diagnosis of genomic imbalance.
PMID 17901113·Clin Chem·2007
4-observational
A newly recognized craniosynostosis syndrome with features of Aarskog-Scott and Teebi syndromes.
PMID 17506099·Am J Med Genet A·2007
8-other
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
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
The biology and management of laryngeal neurofibroma.
PMID 15611399·Arch Otolaryngol Head Neck Surg·2004
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
7101 JAHNKE RD, SUITE 611
RICHMOND, VA 23225

Location

Practice Location

7101 JAHNKE RD, RICHMOND, VA
(804) 327-4046

Quick Facts

NPI
1366402141
Entity Type
Individual
Gender
Female
Medicare
Not confirmed
Specialties
1
Locations
1
Years in Practice
23
Publications
20

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