Filtros de búsqueda

Lista de obras de Vanessa Sotomaior

A 1.5Mb terminal deletion of 12p associated with autism spectrum disorder

artículo científico publicado en 2014

Analysis of polymorphisms in the lactotransferrin gene promoter and dental caries.

artículo científico publicado en 2011

Association between vitamin D receptor gene polymorphisms and susceptibility to chronic kidney disease and periodontitis.

artículo científico publicado en 2007

Association of a PARK2 Germline Variant and Epithelial Ovarian Cancer in a Southern Brazilian Population.

artículo científico publicado en 2016

Chromosome 19p13.3 deletion in a child with Peutz-Jeghers syndrome, congenital heart defect, high myopia, learning difficulties and dysmorphic features: Clinical and molecular characterization of a new contiguous gene syndrome.

artículo científico publicado en 2011

Complement-fixing donor-specific anti-HLA antibodies and kidney allograft failure

artículo científico publicado en 2018

Congenital bilateral absence of the vas deferens as an atypical form of cystic fibrosis: reproductive implications and genetic counseling

artículo científico publicado en 2017

Cystic fibrosis gene variability in two southern Brazilian Amerindian populations: analysis of the deltaF508 mutation and the KM19 and XV2C haplotypes

article

Cystic fibrosis in Afro-Brazilians: XK haplotypes analysis supports the European origin of p.F508del mutation

artículo científico publicado en 2017

Genetic data for 26 autosomal STR markers from Brazilian population

artículo científico publicado en 2018

Interleukin-6 plasmatic levels in patients with head trauma and intracerebral hemorrhage.

artículo científico publicado en 2010

Mosaic partial trisomy 19p12-q13.11 due to a small supernumerary marker chromosome: A locus associated with Asperger syndrome?

artículo científico publicado en 2011

Parkin protein expression and its impact on survival of patients with advanced colorectal cancer

artículo científico publicado en 2018

STR data for 15 autosomal STR markers from Paraná (Southern Brazil)

artículo científico publicado el 25 de abril de 2013

Somatic/gonadal mosaicism in a syndromic form of ectrodactyly, including eye abnormalities, documented through array-based comparative genomic hybridization

artículo científico publicado en 2011

The HLA polymorphsm of two distinctive South-American Indian tribes: The Kaingang and the Guarani

artículo científico publicado en 1993

Transplantation of SNAP-treated adipose tissue-derived stem cells improves cardiac function and induces neovascularization after myocardium infarct in rats

artículo científico publicado en 2010

What can be done when asymptomatic patients discover they have Brugada syndrome? A case report of Brugada syndrome

artículo científico publicado en 2010