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469 results on '"Calvas, Patrick"'

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

2. Congenital microcoria deletion in mouse links Sox21 dysregulation to disease and suggests a role for TGFB2 in glaucoma and myopia

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

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

12. 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

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

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

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

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

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

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

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

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

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

28. Mosaicism detection and impact in eye development anomalies

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

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

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

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

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

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

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

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

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

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

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

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

50. Mutations in WNT10A are frequently involved in oligodontia associated with minor signs of ectodermal dysplasia

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