N. Gardès

发表

Preimplantation genetic diagnosis for achondroplasia: genetics and gynaecological limits and difficulties.

C. Philippe, C. Moutou, N. Gardés, 2003, Human reproduction.

Birth after pre‐implantation genetic diagnosis (PGD) of spinocerebellar ataxia 2 (Sca2)

C. Moutou, N. Gardés, S. Viville, 2008, Prenatal diagnosis.

New tools for preimplantation genetic diagnosis of Huntington's disease and their clinical applications

C. Moutou, N. Gardés, S. Viville, 2004, European Journal of Human Genetics.

Duplex, triplex and quadruplex PCR for the preimplantation genetic diagnosis (PGD) of cystic fibrosis (CF), an exhaustive approach

C. Moutou, S. Viville, N. Gardès, 2004, Prenatal diagnosis.

Multiplex PCR combining deltaF508 mutation and intragenic microsatellites of the CFTR gene for pre-implantation genetic diagnosis (PGD) of cystic fibrosis

C. Moutou, N. Gardés, S. Viville, 2002, European Journal of Human Genetics.

Improving preimplantation genetic diagnosis for Fragile X syndrome: two new powerful single-round multiplex indirect and direct tests

C. Moutou, N. Gardés, C. Rongières, 2015, European Journal of Human Genetics.

Duplex PCR for preimplantation genetic diagnosis (PGD) of spinal muscular atrophy

C. Moutou, N. Gardés, S. Viville, 2003, Prenatal diagnosis.

Allele‐specific amplification for preimplantation genetic diagnosis (PGD) of spinal muscular atrophy

C. Moutou, N. Gardés, C. Rongières, 2001, Prenatal diagnosis.

Strategies and outcomes of PGD of familial adenomatous polyposis.

C. Moutou, N. Gardés, S. Viville, 2007, Molecular human reproduction.

Case report: birth after preimplantation genetic diagnosis of a subtle mutation in SMN1 gene

C. Moutou, N. Gardés, S. Viville, 2006, Prenatal diagnosis.

Preimplantation genetic diagnosis for achondroplasia: genetics and gynaecological limits and dif®culties

C. Philippe, N. Gardés, C. Rongières, 2022 .