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List of works by Myrto Poulou

A study of a single variant allele (rs1426654) of the pigmentation-related gene SLC24A5 in Greek subjects

scientific article

Are ALOX5AP gene SNPs a risk or protective factor for stroke?

scientific article published on 08 July 2014

Association of the CALM1 core promoter polymorphism with knee osteoarthritis in patients of Greek origin

scientific article published on 01 June 2008

BTNL2 gene SNPs as a contributing factor to sarcoidosis pathogenesis in a cohort of Greek patients

scientific article

Complex preimplantation genetic diagnosis for beta-thalassaemia, sideroblastic anaemia, and human leukocyte antigen (HLA)-typing.

scientific article published on 4 December 2015

Congenital cataracts, facial dysmorphism, and neuropathy syndrome

scientific article published on 01 September 2011

Cystic fibrosis conductance regulator, tumor necrosis factor, interferon alpha-10, interferon alpha-17, and interferon gamma genotyping as potential risk markers in pulmonary sarcoidosis pathogenesis in Greek patients

scientific article published on 01 August 2010

Cystic fibrosis genetic counseling difficulties due to the identification of novel mutations in the CFTR gene

scientific article published on 11 February 2012

Genomic screening of ABCA4 and array CGH analysis underline the genetic variability of Greek patients with inherited retinal diseases

scientific article published on 16 February 2016

Melanocortin receptor-1 gene polymorphisms and the risk of cutaneous melanoma in a low-risk southern European population.

scientific article

Multi-allele genotyping platform for the simultaneous detection of mutations in the Wilson disease related ATP7B gene.

scientific article published on 30 October 2015

Phenotypic expression of a spectrum of Neurofibromatosis Type 1 (NF1) mutations identified through NGS and MLPA

article

Prenatal diagnosis for CF using High Resolution Melting Analysis and simultaneous haplotype analysis through QF-PCR

scientific article published on 29 April 2014

Single-cell high resolution melting analysis: A novel, generic, pre-implantation genetic diagnosis (PGD) method applied to cystic fibrosis (HRMA CF-PGD).

scientific article published on 19 October 2015

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