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ARTHUR ZINN, MD
MD
Clinical Genetics (M.D.) Physician
NPI: 1538185400Individual
Specialties, Licenses & Credentials
Clinical Genetics (M.D.) PhysicianPrimary
Medical Genetics — Clinical Genetics (M.D.)
Code: 207SG0201X
35-048122(OH)
Research & Publications (20)
MODY-like diabetes associated with an apparently balanced translocation: possible involvement of MPP7 gene and cell polarity in the pathogenesis of diabetes.
PMID 19216786·Mol Cytogenet·2009
8-other
Effect of ascertainment and genetic features on the phenotype of Klinefelter syndrome.
PMID 18410780·J Pediatr·2008
8-other
EFHC2 SNP rs7055196 is not associated with fear recognition in 45,X Turner syndrome.
PMID 17948898·Am J Med Genet B Neuropsychiatr Genet·2008
8-other
Reassessing the cardiovascular risks and benefits of thiazolidinediones.
PMID 18781598·Clin Cardiol·2008
6-review
Cryptic chromosomal abnormalities identified in children with congenital heart disease.
PMID 18535492·Pediatr Res·2008
4-observational
Refined mapping of X-linked reticulate pigmentary disorder and sequencing of candidate genes.
PMID 18404279·Hum Genet·2008
8-other
Oxytocin deficiency mediates hyperphagic obesity of Sim1 haploinsufficient mice.
PMID 18451093·Mol Endocrinol·2008
7-preclinical
Sequence variation at the human FOXO3 locus: a study of premature ovarian failure and primary amenorrhea.
PMID 17959613·Hum Reprod·2008
7-preclinical
Cognitive and motor development during childhood in boys with Klinefelter syndrome.
PMID 18266239·Am J Med Genet A·2008
4-observational
A Turner syndrome neurocognitive phenotype maps to Xp22.3.
PMID 17517138·Behav Brain Funct·2007
8-other
Mutational analyses of UPIIIA, SHH, EFNB2 and HNF1beta in persistent cloaca and associated kidney malformations.
PMID 17476318·J Pediatr Urol·2007
8-other
Phenotypic expansion of the supernumerary derivative (22) chromosome syndrome: VACTERL and Hirschsprung's disease.
PMID 18022449·J Pediatr Surg·2007
5-case
Dynamic regulation of p53 subnuclear localization and senescence by MORC3.
PMID 17332504·Mol Biol Cell·2007
7-preclinical
Compound heterozygosity of SHOX-encompassing and downstream PAR1 deletions results in Langer mesomelic dysplasia (LMD).
PMID 17394206·Am J Med Genet A·2007
5-case
Giant right atrial wall vegetation mimicking cardiac tumor.
PMID 17600677·J Am Soc Echocardiogr·2007
5-case
The physical phenotype of girls and women with Turner syndrome is not X-imprinted.
PMID 17242899·Hum Genet·2007
8-other
Editorial: MC4R mutations--weight before screening!
PMID 16679511·J Clin Endocrinol Metab·2006
8-other
SIM1 overexpression partially rescues agouti yellow and diet-induced obesity by normalizing food intake.
PMID 16709610·Endocrinology·2006
7-preclinical
Sim1 haploinsufficiency impairs melanocortin-mediated anorexia and activation of paraventricular nucleus neurons.
PMID 16728530·Mol Endocrinol·2006
4-observational
DELETION MAPPING OF CRITICAL REGION FOR HYPOSPADIAS, PENOSCROTAL TRANSPOSITION AND IMPERFORATE ANUS ON HUMAN CHROMOSOME 13.
PMID 17476316·J Pediatr Urol·2006
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
- 11100 EUCLID AVE
CLEVELAND, OH 44106 - Phone
- (216) 844-3936
Quick Facts
- NPI
- 1538185400
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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