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Lista de obras de Victor Ferraz

A further case of a Prader-Willi syndrome phenotype in a patient with Angelman syndrome molecular defect.

artículo científico publicado en 2002

Aggravation of eyelid and conjunctival malignancies following photodynamic therapy in DeSanctis-Cacchione syndrome

artículo científico publicado en 2006

Clinical genetics in developing countries: the case of Brazil

scientific article published on 01 January 2004

Clinical-neurologic, cytogenetic and molecular aspects of the Prader-Willi and Angelman syndromes

scientific article published on 01 June 1997

Contribution of SLC26A4 to the molecular diagnosis of nonsyndromic prelingual sensorineural hearing loss in a Brazilian cohort

article

First description of ultramutated endometrial cancer caused by germline loss-of-function and somatic exonuclease domain mutations in POLE gene

scientific article published on 25 September 2020

Iris coloboma, blepharophimosis, arachnodactyly, joint contractures: Beals syndrome and Van den Ende-Gupta syndrome phenotypic similarities

artículo científico publicado en 2009

Molecular basis of familial adenomatous polyposis in the southeast of Brazil: identification of six novel mutations

artículo científico publicado en 2019

Mucopolysaccharidoses in Brazil: what happens from birth to biochemical diagnosis?

artículo científico publicado en 2008

Recurrent Mutations in the Basic Domain of TWIST2 Cause Ablepharon Macrostomia and Barber-Say Syndromes

artículo científico publicado en 2015

Self-reported cancer family history is a useful tool for identification of individuals at risk of hereditary cancer predisposition syndrome at primary care centers in middle-income settings: a longitudinal study

artículo científico publicado en 2016

TP53 p.R337H prevalence in a series of Brazilian hereditary breast cancer families.

artículo científico publicado en 2014

[How the gynecologist can guide women with a family history of cancer?]

artículo científico publicado en 2014

[Perception of cancer causes and risk, family history and preventive behaviors of users in oncogenetic counseling]

scientific article published on 01 April 2013