Universal strategy for preimplantation genetic testing for cystic fibrosis based on next generation sequencing

Clinical application of a protocol based on universal next-generation sequencing for the diagnosis of beta-thalassaemia and sickle cell anaemia in preimplantation embryos

(2018) Nada Kubikova et al.   REPRODUCTIVE BIOMEDICINE ONLINE

The decision on the embryo to transfer after Preimplantation Genetic Diagnosis for X-autosome reciprocal translocation in male carrier

(2018) Sandrine Chamayou et al.   Molecular Cytogenetics

The accumulation of vitrified oocytes is a strategy to increase the number of euploid available blastocysts for transfer after preimplantation genetic testing

(2017) Sandrine Chamayou et al.   JOURNAL OF ASSISTED REPRODUCTION AND GENETICS

The improvement of the best practice guidelines for preimplantation genetic diagnosis of cystic fibrosis: toward an international consensus

(2015) Anne Girardet et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

ESHRE PGD Consortium data collection XIII: cycles from January to December 2010 with pregnancy follow-up to October 2011

(2015) M. De Rycke et al.   HUMAN REPRODUCTION

Validation of a semiconductor next-generation sequencing assay for the clinical genetic screening ofCFTR

(2015) Daniel Trujillano et al.   Molecular Genetics & Genomic Medicine

Preimplantation genetic diagnosis for cystic fibrosis: the Montpellier center's 10-year experience

(2014) A. Girardet et al.   CLINICAL GENETICS

Consequences of metaphase II oocyte cryopreservation on mRNA content

(2011) S. Chamayou et al.   CRYOBIOLOGY

Mutation nomenclature in practice: Findings and recommendations from the cystic fibrosis external quality assessment scheme

(2011) Sarah Berwouts et al.   HUMAN MUTATION

Recommendations for the classification of diseases as CFTR-related disorders

(2011) C. Bombieri et al.   Journal of Cystic Fibrosis

Cystic fibrosis testing 8 years on: Lessons learned from carrier screening and sequencing analysis

(2010) Charles M Strom et al.   GENETICS IN MEDICINE

Molecular analysis of mutations and polymorphisms in the CFTR gene in male infertility

(2010) L Tamburino et al.   REPRODUCTIVE BIOMEDICINE ONLINE

Best practice guidelines for molecular genetic diagnosis of cystic fibrosis and CFTR-related disorders – updated European recommendations

(2008) Els Dequeker et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Genetic Investigations of CFTR Mutations in Congenital Absence of Vas Deferens, Uterus, and Vagina as a Cause of Infertility

(2008) R. Radpour et al.   JOURNAL OF ANDROLOGY