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MARK ZENKER, M.D.
M.D.
Cardiovascular Disease Physician
NPI: 1316985120IndividualAccepts Medicare
Specialties, Licenses & Credentials
Cardiovascular Disease PhysicianPrimary
Internal Medicine — Cardiovascular Disease
Code: 207RC0000X
21038(TN)
CMS Specialties
PrimaryCARDIOVASCULAR DISEASE (CARDIOLOGY)
Education
SOUTHERN ILLINOIS UNIVERSITY SCHOOL OF MEDICINE
Class of 1989
Research & Publications (20)
Oculopharyngeal muscular dystrophy as a rare differential diagnosis for unexplained dysphagia: a case report.
PMID 19175930·Cases J·2009
8-other
Further clinical and molecular delineation of the 9q subtelomeric deletion syndrome supports a major contribution of EHMT1 haploinsufficiency to the core phenotype.
PMID 19264732·J Med Genet·2009
8-other
Craniosynostosis in patients with Noonan syndrome caused by germline KRAS mutations.
PMID 19396835·Am J Med Genet A·2009
5-case
Genetics of nephrotic syndrome: new insights into molecules acting at the glomerular filtration barrier.
PMID 19649571·J Mol Med (Berl)·2009
6-review
Independent NF1 and PTPN11 mutations in a family with neurofibromatosis-Noonan syndrome.
PMID 19449407·Am J Med Genet A·2009
5-case
A large-scale mutation search reveals genetic heterogeneity in 3M syndrome.
PMID 19225462·Eur J Hum Genet·2009
8-other
Infantile hypophosphatasia due to a new compound heterozygous TNSALP mutation - functional evidence for a hydrophobic side-chain?
PMID 18523927·Exp Clin Endocrinol Diabetes·2009
5-case
SMARCAL1 mutations: a cause of prepubertal idiopathic steroid-resistant nephrotic syndrome.
PMID 19127206·Pediatr Res·2009
5-case
Goltz-Gorlin (focal dermal hypoplasia) and the microphthalmia with linear skin defects (MLS) syndrome: no evidence of genetic overlap.
PMID 19277062·Eur J Hum Genet·2009
8-other
The spectra of clinical phenotypes in aplasia cutis congenita and terminal transverse limb defects.
PMID 19610107·Am J Med Genet A·2009
5-case
Multiple giant cell lesions in patients with Noonan syndrome and cardio-facio-cutaneous syndrome.
PMID 18854871·Eur J Hum Genet·2009
8-other
Local clustering of PRSS1 R122H mutations in hereditary pancreatitis patients from Northern Germany.
PMID 18702646·Am J Gastroenterol·2008
4-observational
Clinical and molecular delineation of the 17q21.31 microdeletion syndrome.
PMID 18628315·J Med Genet·2008
8-other
Johanson-Blizzard syndrome: report of a novel mutation and severe liver involvement.
PMID 18553553·Am J Med Genet A·2008
5-case
Analysis of genes encoding laminin beta2 and related proteins in patients with Galloway-Mowat syndrome.
PMID 18594871·Pediatr Nephrol·2008
8-other
Clinical and genetic distinction of Schimke immuno-osseous dysplasia and cartilage-hair hypoplasia.
PMID 18627050·Am J Med Genet A·2008
8-other
No mutation in genes of the WNT signaling pathway in patients with Zimmermann-Laband syndrome.
PMID 18541964·Clin Dysmorphol·2008
8-other
Johanson-Blizzard syndrome caused by identical UBR1 mutations in two unrelated girls, one with a cardiomyopathy.
PMID 19006206·Am J Med Genet A·2008
5-case
Johanson-Blizzard syndrome with mild phenotypic features confirmed by UBR1 gene testing.
PMID 19058315·World J Gastroenterol·2008
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
- 4230 HARDING RD, SUITE 330
NASHVILLE, TN 37205 - Phone
- (615) 269-4545
Quick Facts
- NPI
- 1316985120
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Accepted
- Specialties
- 1
- Locations
- 1
- Years in Practice
- 37
- Publications
- 20
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