Back to Search
MARY IRONS, PHD
PHD
Clinical Psychologist
NPI: 1831290246Individual
Specialties, Licenses & Credentials
Clinical PsychologistPrimary
Psychologist — Clinical
Code: 103TC0700X
0810003324(VA)
Research & Publications (20)
Mental status screening of emergency department patients: normative study of the quick confusion scale.
PMID 12359535·Acad Emerg Med·2002
3-trial
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
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
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
- 198 SPOTNAP ROAD, SUITE A3
CHARLOTTESVILLE, VA 22902 - Phone
- (434) 963-0324
Quick Facts
- NPI
- 1831290246
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
Are you this provider?
Claim Your Profile