Back to Search

WHITMAN REARDON, MD

MD

Internal Medicine Physician

NPI: 1598792277IndividualAccepts Medicare

Specialties, Licenses & Credentials

Internal Medicine PhysicianPrimary

Internal Medicine

Code: 207R00000X

35477(NC)

CMS Specialties

PrimaryINTERNAL MEDICINE

Education

UNIVERSITY OF NORTH CAROLINA AT CHAPEL HILL SCHOOL OF MEDICINE

Class of 1990

Research & Publications (20)

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
Integrity of nuclear genomic deoxyribonucleic acid in cooked meat: Implications for food traceability.
PMID 18791146·J Anim Sci·2009
8-other
Evolution of flower shape in Plantago lanceolata.
PMID 19593661·Plant Mol Biol·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
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
Job syndrome masquerading as non-accidental injury.
PMID 17804589·Arch Dis Child·2008
5-case
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
Nephrocalcinosis and disordered calcium metabolism in two children with SHORT syndrome.
PMID 18384141·Am J Med Genet A·2008
5-case
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
Clinical and radiological findings in Schinzel-Giedion syndrome.
PMID 18461363·Eur J Pediatr·2008
5-case
Low-grade fibromyxoid sarcoma: yet another malignancy associated with Kabuki syndrome.
PMID 18541969·Clin Dysmorphol·2008
5-case
Pregnancy and perinatal outcomes after assisted reproduction: a comparative study.
PMID 18521653·Ir J Med Sci·2008
4-observational
Recurrent rearrangements of chromosome 1q21.1 and variable pediatric phenotypes.
PMID 18784092·N Engl J Med·2008
8-other
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
A survey of assisted reproductive technology births and imprinting disorders.
PMID 17921133·Hum Reprod·2007
4-observational
Bilateral optic disk swelling in the 4q34 deletion syndrome.
PMID 17933677·J AAPOS·2007
5-case
Congenital ulcerating hemangioma in a baby with KRAS mutation and cardio-facio-cutaneous syndrome.
PMID 17551339·Clin Dysmorphol·2007
5-case
Kallmann syndrome presenting as congenital ptosis in brothers.
PMID 17551340·Clin Dysmorphol·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
940 MARTIN LUTHER KING JR BLVD
CHAPEL HILL, NC 27514

Location

Practice Location

940 MARTIN LUTHER KING JR BLVD, CHAPEL HILL, NC
(919) 942-5123

Quick Facts

NPI
1598792277
Entity Type
Individual
Gender
Female
Medicare
Accepted
Specialties
1
Locations
1
Years in Practice
36
Publications
20

Are you this provider?

Claim Your Profile