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1. Episignatures in practice: independent evaluation of published episignatures for the molecular diagnostics of ten neurodevelopmental disorders

3. A Solve-RD ClinVar-based reanalysis of 1522 index cases from ERN-ITHACA reveals common pitfalls and misinterpretations in exome sequencing

4. Unsuspected consequences of synonymous and missense variants in OCA2 can be detected in blood cell RNA samples of patients with albinism.

5. La caverne

6. Fifteen years of research on oral–facial–digital syndromes: from 1 to 16 causal genes

7. A second cohort of CHD3 patients expands the molecular mechanisms known to cause Snijders Blok-Campeau syndrome

9. Episignatures in practice: independent evaluation of published episignatures for the molecular diagnostics of ten neurodevelopmental disorders

10. Unsuspected consequences of synonymous and missense variants in OCA2 can be detected in blood cell RNA samples of patients with albinism

11. Unsuspected consequences of synonymous and missense variants inOCA2can be detected in blood cell RNA samples of patients with albinism

12. A Solve-RD ClinVar-based reanalysis of 1522 index cases from ERN-ITHACA reveals common pitfalls and misinterpretations in exome sequencing

13. MED13L-related intellectual disability: involvement of missense variants and delineation of the phenotype

15. A Solve-RD ClinVar-based reanalysis of 1522 index cases from ERN-ITHACA reveals common pitfalls and misinterpretations in exome sequencing

17. Episignatures in practice: independent evaluation of published episignatures for the molecular diagnostics of ten neurodevelopmental disorders

20. First evidence of <scp> SOX2 </scp> mutations in Peters' anomaly: Lessons from molecular screening of 95 patients

21. Phenotypic spectrum and transcriptomic profile associated with germline variants in TRAF7

22. Gain of function due to increased opening probability by two KCNQ5 pore variants causing developmental and epileptic encephalopathy

24. Gain of function due to increased opening probability by two

26. De novo microdeletions and point mutations affecting SOX2 in three individuals with intellectual disability but without major eye malformations

29. Gain of function due to increased opening probability by two KCNQ5 pore variants causing developmental and epileptic encephalopathy

30. Novel NEK8 Mutations Cause Severe Syndromic Renal Cystic Dysplasia through YAP Dysregulation.

31. A second cohort of CHD3 patients expands the molecular mechanisms known to cause Snijders Blok-Campeau syndrome

32. Neurodevelopmental phenotype associated with CHD8-SUPT16H duplication

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

34. A series of 38 novel germline and somatic mutations of NIPBL in Cornelia de Lange syndrome

36. A targeted next-generation sequencing assay for the molecular diagnosis of genetic disorders with orodental involvement

37. Severe phenotype in patients with large deletions of NF1

38. Severe Phenotype in Patients with Large Deletions of NF1

39. Pycnodysostosis: Natural history and management guidelines from 27 French cases and a literature review

41. Refinement of Genotype-Phenotype Correlation in 18 Patients Carrying a 1q24q25 Deletion

42. Prevalence and management of gastrointestinal manifestations in Silver–Russell syndrome

43. A Study of the Clinical and Radiological Features in a Cohort of 93 Patients with a COL2A1 Mutation Causing Spondyloepiphyseal Dysplasia Congenita or a Related Phenotype

44. Dissection of contiguous gene effects for deletions around ERF on chromosome 19

46. The clinical significance of small copy number variants in neurodevelopmental disorders

47. Deletions in the 3′ Part of the NFIX Gene Including a Recurrent Alu-Mediated Deletion of Exon 6 and 7 Account for Previously Unexplained Cases of Marshall–Smith Syndrome

48. Bilateral periventricular nodular heterotopia in France: frequency of mutations in FLNA, phenotypic heterogeneity and spectrum of mutations

49. Clinical manifestations in patients with SOS1 mutations range from Noonan syndrome to CFC syndrome

50. Multiplex targeted high‐throughput sequencing in a series of 352 patients with congenital limb malformations

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