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WILLIAM REARDON, DMD
DMD
General Practice Dentistry
NPI: 1538380720Individual
Specialties, Licenses & Credentials
General Practice DentistryPrimary
Dentist — General Practice
Code: 1223G0001X
DS020495(PA)
Research & Publications (20)
Evidence for digenic inheritance in some cases of Antley-Bixler syndrome?
PMID 10633130·J Med Genet·2000
8-other
Integrity of nuclear genomic deoxyribonucleic acid in cooked meat: Implications for food traceability.
PMID 18791146·J Anim Sci·2009
8-other
Aplasia of cochlear nerves and olfactory bulbs in association with SOX10 mutation.
PMID 19208381·Am J Med Genet A·2009
5-case
Classic and atypical fibrodysplasia ossificans progressiva (FOP) phenotypes are caused by mutations in the bone morphogenetic protein (BMP) type I receptor ACVR1.
PMID 19085907·Hum Mutat·2009
8-other
Pseudoarthrosis of the clavicle and copper beaten skull associated with chromosome 10p11.21p12.1 microdeletion.
PMID 18080323·Am J Med Genet A·2008
5-case
Clinical and molecular characteristics of 1qter microdeletion syndrome: delineating a critical region for corpus callosum agenesis/hypogenesis.
PMID 18178631·J Med Genet·2008
5-case
Nephrocalcinosis and disordered calcium metabolism in two children with SHORT syndrome.
PMID 18384141·Am J Med Genet A·2008
5-case
Clinical and radiological findings in Schinzel-Giedion syndrome.
PMID 18461363·Eur J Pediatr·2008
5-case
Pregnancy and perinatal outcomes after assisted reproduction: a comparative study.
PMID 18521653·Ir J Med Sci·2008
4-observational
Low-grade fibromyxoid sarcoma: yet another malignancy associated with Kabuki syndrome.
PMID 18541969·Clin Dysmorphol·2008
5-case
Recurrent rearrangements of chromosome 1q21.1 and variable pediatric phenotypes.
PMID 18784092·N Engl J Med·2008
8-other
Dissecting the molecular mechanisms in craniofrontonasal syndrome: differential mRNA expression of mutant EFNB1 and the cellular mosaic.
PMID 18043713·Eur J Hum Genet·2008
4-observational
A survey of assisted reproductive technology births and imprinting disorders.
PMID 17921133·Hum Reprod·2007
4-observational
Kallmann syndrome presenting as congenital ptosis in brothers.
PMID 17551340·Clin Dysmorphol·2007
5-case
WT1 mutations in Meacham syndrome suggest a coelomic mesothelial origin of the cardiac and diaphragmatic malformations.
PMID 17853480·Am J Med Genet A·2007
5-case
Kidney failure in Townes-Brocks syndrome: an under recognized phenomenon?
PMID 17910067·Am J Med Genet A·2007
5-case
Deletions at the SOX10 gene locus cause Waardenburg syndrome types 2 and 4.
PMID 17999358·Am J Hum Genet·2007
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
- 35 W PENNSYLVANIA AVE
DOWNINGTOWN, PA 19335 - Phone
- (610) 269-0489
Quick Facts
- NPI
- 1538380720
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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