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GINA FERRERO, MD
MD
Rheumatology Physician
NPI: 1962923086IndividualAccepts Medicare
Specialties, Licenses & Credentials
Internal Medicine Physician
Internal Medicine
Code: 207R00000X
MD211234(OR)
Student in an Organized Health Care Education/Training Program
Student in an Organized Health Care Education/Training Program
Code: 390200000X
Rheumatology PhysicianPrimary
Internal Medicine — Rheumatology
Code: 207RR0500X
MD211234(OR)
CMS Specialties
PrimaryRHEUMATOLOGY
Education
OTHER
Class of 2016
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
Phenotype resembling Donnai-Barrow syndrome in a patient with 9qter;16qter unbalanced translocation.
PMID 16532464·Am J Med Genet A·2006
5-case
Pachygyria and cerebellar hypoplasia in a patient with a 2q22-q23 deletion that includes the ZFHX1B gene.
PMID 15103730·Am J Med Genet A·2004
8-other
Oral, facial, digital, vertebral anomalies with psychomotor delay: a mild form of OFD type Gabrielli?
PMID 12439899·Am J Med Genet·2002
5-case
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
Germline BRAF mutations in Noonan, LEOPARD, and cardiofaciocutaneous syndromes: molecular diversity and associated phenotypic spectrum.
PMID 19206169·Hum Mutat·2009
8-other
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
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
Via practice · 2 locations total
- Address
- 1 COOPER PLZ
CAMDEN, NJ 08103 - Phone
- (856) 342-2000
Quick Facts
- NPI
- 1962923086
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Accepted
- Specialties
- 3
- Locations
- 2
- Years in Practice
- 10
- Publications
- 20
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