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5. Secondary findings from whole-exome/genome sequencing evaluating stakeholder perspectives. A review of the literature

11. Additional file 1 of Cost of exome analysis in patients with intellectual disability: a micro-costing study in a French setting

13. EP06.12: Prospective reanalysis of unsolved prenatal exome sequencing: diagnostic yield and contribution of postnatal/post‐mortem findings.

23. ESSAI RANDOMISE POUR EVALUER L EFFICACITE ET LA SECURITE DE TRAITEMENTS CHEZ DES PATIENTS AMBULATOIRES ATTEINTS DE COVID-19 AYANT DES FACTEURS DE RISQUE - ESSAI COVERAGE FRANCE

25. Clinical reappraisal of SHORT syndrome with PIK3R1 mutations: toward recommendation for molecular testing and management

26. OP10.09: Prenatal exome sequencing: a powerful tool to improve description of prenatal features related to genetic disorders.

32. Plateforme COVERAGE France : un essai clinique randomisé multicentrique utilisant un schéma adaptatif multi-bras multi-étape (MAMS) pour évaluer plusieurs traitements expérimentaux de la COVID-19 en ambulatoire

33. ESSAI RANDOMISÉ POUR ÉVALUER L’EFFICACITÉ ET LA SÉCURITÉ DE TRAITEMENTS CHEZ DES PATIENTS AMBULATOIRES ATTEINTS DE COVID-19 AYANT DES FACTEURS DE RISQUE ESSAI COVERAGE FRANCE : PRÉSENTATION DU PROTOCOLE

34. Impact psychologique de la pandémie de COVID-19 sur les soignants

38. Systematic molecular and cytogenetic screening of 100 patients with marfanoid syndromes and intellectual disability

39. Riesgos infecciosos alimentarios y embarazo: ¿cuál es la información de la que disponen los profesionales de la salud?

40. Effect of mutation type and location on clinical outcome in 1,013 probands with marfan syndrome or related phenotypes and FBN1 mutations: an international study

42. The Decreasing Prevalence of Nonrefractive Visual Impairment in Older Europeans: A Meta-analysis of Published and Unpublished Data

47. The new Ghent criteria for Marfan syndrome: what do they change?

50. The very low penetrance of cystic fibrosis for the R117H mutation: a reappraisal for genetic counselling and newborn screening

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