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Your search keyword '"Calvas, Patrick"' showing total 9 results

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9 results on '"Calvas, Patrick"'

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1. Attitudes of French populations towards the disclosure of unsolicited findings in medical genetics.

2. Outcomes of 4 years of molecular genetic diagnosis on a panel of genes involved in premature aging syndromes, including laminopathies and related disorders.

3. Safety and efficacy of riluzole in spinocerebellar ataxia type 2 in France (ATRIL): a multicentre, randomised, double-blind, placebo-controlled trial.

4. Mapping of Spinocerebellar Ataxia 13 to Chromosome 19q13.3-q13.4 in a Family with Autosomal Dominant Cerebellar Ataxia and Mental Retardation.

5. The HNF1B score is a simple tool to select patients for HNF1B gene analysis.

6. Relative frequencies of inherited retinal dystrophies and optic neuropathies in Southern France: assessment of 21-year data management.

7. A genome-wide association study provides evidence for association of chromosome 8p23 (MYP10) and 10q21.1 (MYP15) with high myopia in the French Population.

8. Linkage analysis of high myopia susceptibility locus in 26 families.

9. Contribution of ABCC6 genomic rearrangements to the diagnosis of pseudoxanthoma elasticum in French patients.

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