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ROBERTO ZORI, MD
MD
Clinical Genetics (M.D.) Physician
NPI: 1407887250Individual
Specialties, Licenses & Credentials
Clinical Genetics (M.D.) PhysicianPrimary
Medical Genetics — Clinical Genetics (M.D.)
Code: 207SG0201X
ME54105(FL)
Research & Publications (20)
Chromosome 8p23.1 deletions as a cause of complex congenital heart defects and diaphragmatic hernia.
PMID 19606479·Am J Med Genet A·2009
5-case
Reversal of glycogen storage disease type IIIa-related cardiomyopathy with modification of diet.
PMID 19322675·J Inherit Metab Dis·2009
5-case
Long-term disease control of refractory anaplastic large cell lymphoma with vinblastine.
PMID 19194204·J Pediatr Hematol Oncol·2009
5-case
Molecular cytogenetic characterization of two small supernumerary marker chromosomes derived from chromosome 19.
PMID 19133694·Am J Med Genet A·2009
5-case
Aldehyde dehydrogenase activity as a functional marker for lung cancer.
PMID 18952074·Chem Biol Interact·2009
7-preclinical
In vivo expression of human ATP:cob(I)alamin adenosyltransferase (ATR) using recombinant adeno-associated virus (rAAV) serotypes 2 and 8.
PMID 17471589·J Gene Med·2007
7-preclinical
Chromosome painting in the manatee supports Afrotheria and Paenungulata.
PMID 17244368·BMC Evol Biol·2007
7-preclinical
High cognitive functioning and behavioral phenotype in Pallister-Killian syndrome.
PMID 16906561·Am J Med Genet A·2006
5-case
Telegenetic medicine: improved access to services in an underserved area.
PMID 16774698·J Telemed Telecare·2006
8-other
Lupus-like disease and high interferon levels corresponding to trisomy of the type I interferon cluster on chromosome 9p.
PMID 16645992·Arthritis Rheum·2006
5-case
Diagnosis of an early precursor-B-ALL presenting with hypereosinophilia using FISH on immunomagnetically selected CD19+ cells.
PMID 16166969·Clin Adv Hematol Oncol·2005
5-case
Fine mapping of chromosome 17 translocation breakpoints > or = 900 Kb upstream of SOX9 in acampomelic campomelic dysplasia and a mild, familial skeletal dysplasia.
PMID 15717285·Am J Hum Genet·2005
8-other
Locus control region elements HS2 and HS3 in combination with chromatin boundaries confer high-level expression of a human beta-globin transgene in a centromeric region.
PMID 15507116·Genes Cells·2004
7-preclinical
A molecular diagnosis of hyperparathyroidism-jaw tumor syndrome in an adolescent with recurrent kidney stones.
PMID 15480389·J Pediatr·2004
5-case
Blood lymphocyte chimerism associated with IVF and monochorionic dizygous twinning: case report.
PMID 15375077·Hum Reprod·2004
5-case
Unexpected death and critical illness in Prader-Willi syndrome: report of ten individuals.
PMID 14699614·Am J Med Genet A·2004
5-case
Translocation (X;20)(q13.1;q13.3) as a primary chromosomal finding in two patients with myelocytic disorders.
PMID 12606138·Cancer Genet Cytogenet·2003
5-case
Routine cytogenetic and FISH studies for 17p11/15q11 duplications and subtelomeric rearrangement studies in children with autism spectrum disorders.
PMID 12567405·Am J Med Genet A·2003
8-other
Concurrence of fragile X syndrome and 47, XYY in an individual with a Prader-Willi-like phenotype.
PMID 12494438·Am J Med Genet A·2003
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
- 1600 SW ARCHER RD
GAINESVILLE, FL 32610 - Phone
- (352) 392-4104
Quick Facts
- NPI
- 1407887250
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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