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MARK DEARDORFF, M.D.
M.D.
Pediatrics Physician
NPI: 1700859592Individual
Specialties, Licenses & Credentials
Research & Publications (12)
A 781-kb deletion of 13q12.3 in a patient with Peters plus syndrome.
PMID 19610101·Am J Med Genet A·2009
5-case
Transcriptional dysregulation in NIPBL and cohesin mutant human cells.
PMID 19468298·PLoS Biol·2009
8-other
Dosage effects of cohesin regulatory factor PDS5 on mammalian development: implications for cohesinopathies.
PMID 19412548·PLoS One·2009
7-preclinical
Complex management of a patient with a contiguous Xp11.4 gene deletion involving ornithine transcarbamylase: a role for detailed molecular analysis in complex presentations of classical diseases.
PMID 18524659·Mol Genet Metab·2008
5-case
Mutations in cohesin complex members SMC3 and SMC1A cause a mild variant of cornelia de Lange syndrome with predominant mental retardation.
PMID 17273969·Am J Hum Genet·2007
8-other
Townes-Brocks syndrome: twenty novel SALL1 mutations in sporadic and familial cases and refinement of the SALL1 hot spot region.
PMID 17221874·Hum Mutat·2007
8-other
The value of the metabolic autopsy in the pediatric hospital setting.
PMID 16769386·J Pediatr·2006
8-other
Ganglioglioma in a Sotos syndrome patient with an NSD1 deletion.
PMID 15455365·Am J Med Genet A·2004
5-case
Kermit, a frizzled interacting protein, regulates frizzled 3 signaling in neural crest development.
PMID 11585793·Development·2001
7-preclinical
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 120 S VAL VISTA DR
GILBERT, AZ 85296 - Phone
- (480) 733-6500
Quick Facts
- NPI
- 1700859592
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 12
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