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1. Clinical and functional heterogeneity associated with the disruption of retinoic acid receptor beta

6. ITPR1: The missing gene in miosis–ataxia syndrome?

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

10. Modeling the critical MCOR-causing deletion in mouse unveils aberrantSox21expression in developing and adult iris and ciliary body, and implicatesTgfβ2in MCOR-associated glaucoma and myopia

12. Structural Variant Disrupting the Expression of the Remote FOXC1 Gene in a Patient with Syndromic Complex Microphthalmia.

14. Recurrent heterozygous PAX6 missense variants cause severe bilateral microphthalmia via predictable effects on DNA–protein interaction

15. ATP8A2-related disorders as recessive cerebellar ataxia

16. Searching for secondary findings: considering actionability and preserving the right not to know

17. Expanding the phenotype of the X-linked BCOR microphthalmia syndromes

19. Single Circulating Fetal Trophoblastic Cells Eligible for Non Invasive Prenatal Diagnosis: the Exception Rather than the Rule

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

21. Minigene Splicing Assays and Long-Read Sequencing to Unravel Pathogenic Deep-Intronic Variants in PAX6 in Congenital Aniridia

22. Correction to: Evaluation of somatic and/or germline mosaicism in congenital malformation of the eye

23. Individuals with heterozygous variants in the Wnt-signalling pathway gene FZD5 delineate a phenotype characterized by isolated coloboma and variable expressivity

25. Individuals with heterozygous variants in the Wnt-signalling pathway gene FZD5 delineate a phenotype characterized by isolated coloboma and variable expressivity

26. Mosaicism detection and impact in eye development anomalies

29. Bi-allelic variants inWNT7Bdisrupt the development of multiple organs in humans

30. Protocole national de diagnostic et de soins (PNDS) de l’aniridie congénitale : synthèse pour le médecin traitant

31. Validation of a clinical practice-based algorithm for the diagnosis of autosomal recessive cerebellar ataxias based on NGS identified cases

34. First evidence ofSOX2mutations in Peters' anomaly: Lessons from molecular screening of 95 patients

35. High rate of hypomorphic variants as the cause of inherited ataxia and related diseases: study of a cohort of 366 families

36. Delayed-Onset Friedreichʼs Ataxia Revisited

38. Bi-allelic variants in WNT7Bdisrupt the development of multiple organs in humans

39. Alteration of ornithine metabolism leads to dominant and recessive hereditary spastic paraplegia

42. Molecular findings and clinical data in a cohort of 150 patients with anophthalmia/microphthalmia

43. Activation of cryptic donor splice sites by non-coding and coding PAX6 variants contributes to congenital aniridia

45. Activation of cryptic donor splice sites by non-coding and coding PAX6 variants contributes to congenital aniridia.

46. Lessons learned from 40 novel PIGA patients and a review of the literature

47. De Novo Missense Variants in FBXW11 Cause Diverse Developmental Phenotypes Including Brain, Eye, and Digit Anomalies

48. Mutations in NMNAT1 cause Leber congenital amaurosis with early-onset severe macular and optic atrophy

49. X-linked mental retardation and autism are associated with a mutation in the NLGN4 gene, a member of the neuroligin family

50. Whole exome sequencing identifies a mutation for a novel form of corneal intraepithelial dyskeratosis

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