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GREGG FERRERO, M.D.
M.D.
Orthopaedic Surgery Physician
NPI: 1629033592IndividualAccepts Medicare
Specialties, Licenses & Credentials
Orthopaedic Surgery PhysicianPrimary
Orthopaedic Surgery
Code: 207X00000X
D0059983(MD)
Education
GEORGETOWN UNIVERSITY SCHOOL OF MEDICINE
Class of 1991
Research & Publications (20)
An atypical 7q11.23 deletion in a normal IQ Williams-Beuren syndrome patient.
PMID 19568270·Eur J Hum Genet·2010
5-case
A heritable cause of cleft lip and palate--Van der Woude syndrome caused by a novel IRF6 mutation. Review of the literature and of the differential diagnosis.
PMID 19536562·Eur J Pediatr·2010
5-case
Germline BRAF mutations in Noonan, LEOPARD, and cardiofaciocutaneous syndromes: molecular diversity and associated phenotypic spectrum.
PMID 19206169·Hum Mutat·2009
8-other
A novel H208D TP63 mutation in a familial case of ectrodactyly-ectodermal dysplasia-cleft lip/palate syndrome without clefting.
PMID 19663851·Clin Exp Dermatol·2009
5-case
Subtelomeric FISH analysis in 76 patients with syndromic developmental delay/intellectual disability.
PMID 19490664·Ital J Pediatr·2009
8-other
Inherited and Sporadic Epimutations at the IGF2-H19 locus in Beckwith-Wiedemann syndrome and Wilms' tumor.
PMID 19293570·Endocr Dev·2009
6-review
Cardioprotective effect of dexrazoxane in patients with breast cancer treated with anthracyclines in adjuvant setting: a 10-year single institution experience.
PMID 18690759·Am J Cardiovasc Drugs·2008
8-other
In vivo specific reduction of arylsulfatase B enzymatic activity in children with cystic fibrosis.
PMID 18299243·Mol Genet Metab·2008
8-other
Cryptic deletions are a common finding in "balanced" reciprocal and complex chromosome rearrangements: a study of 59 patients.
PMID 17766364·J Med Genet·2007
4-observational
Integrated strategy for fast and automated molecular characterization of genes involved in craniosynostosis.
PMID 17693524·Clin Chem·2007
8-other
Spontaneous occlusion of brainstem arteriovenous malformation following ligature of a hepatic patent ductus venosus. Case report and review of the literature.
PMID 17330544·J Neurosurg·2007
5-case
N-Terminal c-Fos tyrosine phosphorylation regulates c-Fos/ER association and c-Fos-dependent phospholipid synthesis activation.
PMID 17160021·Oncogene·2007
8-other
Mechanisms causing imprinting defects in familial Beckwith-Wiedemann syndrome with Wilms' tumour.
PMID 17158821·Hum Mol Genet·2007
5-case
Phenotype resembling Donnai-Barrow syndrome in a patient with 9qter;16qter unbalanced translocation.
PMID 16532464·Am J Med Genet A·2006
5-case
Mutation analysis of the NSD1 gene in a group of 59 patients with congenital overgrowth.
PMID 15742365·Am J Med Genet A·2005
4-observational
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 16 N LA PLATA CT
LA PLATA, MD 20646 - Phone
- (301) 392-3330
Quick Facts
- NPI
- 1629033592
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Accepted
- Specialties
- 1
- Locations
- 1
- Years in Practice
- 35
- Publications
- 20
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