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MIRANDA RIEGEL, DO
DO
Emergency Medicine Physician
NPI: 1912646902IndividualAccepts Medicare
Specialties, Licenses & Credentials
Emergency Medicine PhysicianPrimary
Emergency Medicine
Code: 207P00000X
DO-06992(IA)
CMS Specialties
PrimaryEMERGENCY MEDICINE
Education
DES MOINES UNIVERSITY OF OSTEOPATHIC MEDICINE AND HEALTH SCIENCES
Class of 2022
Research & Publications (20)
Persistent low thymic activity and non-cardiac mortality in children with chromosome 22q11.2 microdeletion and partial DiGeorge syndrome.
PMID 19040613·Clin Exp Immunol·2009
8-other
Inv dup del(4)(:p13-->p16.3::p16.3-->qter) in a girl without typical manifestations of Wolf-Hirschhorn syndrome.
PMID 19449429·Am J Med Genet A·2009
5-case
Thirty-two new cases with small supernumerary marker chromosomes detected in connection with fertility problems: detailed molecular cytogenetic characterization and review of the literature.
PMID 18506363·Int J Mol Med·2008
8-other
Monochorionic-diamniotic twins discordant in gender from a naturally conceived pregnancy through postzygotic sex chromosome loss in a 47,XXY zygote.
PMID 18567067·Prenat Diagn·2008
5-case
Duplications in addition to terminal deletions are present in a proportion of ring chromosomes: clues to the mechanisms of formation.
PMID 18006671·J Med Genet·2008
8-other
The fate of children with microdeletion 22q11.2 syndrome and congenital heart defect: clinical course and cardiac outcome.
PMID 17906889·Pediatr Cardiol·2008
8-other
Long-term follow-up of a 26-year-old male with duplication of 16p: clinical report and review.
PMID 17230490·Am J Med Genet A·2007
5-case
Self-organized critical noise amplification in human closed loop control.
PMID 18946526·Front Comput Neurosci·2007
8-other
Cryptic deletions are a common finding in "balanced" reciprocal and complex chromosome rearrangements: a study of 59 patients.
PMID 17766364·J Med Genet·2007
4-observational
Trisomy 18: changes in sex ratio during intrauterine life.
PMID 17022073·Am J Med Genet A·2006
8-other
Postzygotic isochromosome formation as a cause for false-negative results from chorionic villus chromosome examinations.
PMID 16475225·Prenat Diagn·2006
8-other
An unusual reciprocal translocation detected by subtelomeric FISH: interstitial and not terminal.
PMID 15809996·Am J Med Genet A·2005
5-case
Mosaic imprinting defect in a patient with an almost typical expression of the Prader-Willi syndrome.
PMID 15578038·Eur J Hum Genet·2005
5-case
Opitz "C" trigonocephaly-like syndrome in a patient with terminal deletion of 2p and partial duplication of 17q.
PMID 15540175·Am J Med Genet A·2004
5-case
De novo complex chromosome rearrangement: a study of two patients.
PMID 15517822·Genet Couns·2004
5-case
Non-random asynchronous replication at 22q11.2 favours unequal meiotic crossovers leading to the human 22q11.2 deletion.
PMID 15173225·J Med Genet·2004
8-other
No evidence of submicroscopic deletion or segmental uniparental disomy within the candidate regions 7p11.2-p13 and 7q31-qter in a series of non-uniparental disomy Silver-Russell syndrome cases.
PMID 12919141·Clin Genet·2003
8-other
New case of non-mosaic tetrasomy 9p in a severely polymalformed newborn girl.
PMID 14745919·Birth Defects Res A Clin Mol Teratol·2003
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
- 4500 UTICA RIDGE RD
BETTENDORF, IA 52722 - Phone
- (563) 742-5000
Quick Facts
- NPI
- 1912646902
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Accepted
- Specialties
- 1
- Locations
- 1
- Years in Practice
- 4
- Publications
- 20
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