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

2. Bi-allelic TTI1 variants cause an autosomal-recessive neurodevelopmental disorder with microcephaly

3. The clinical and molecular spectrum of the KDM6B-related neurodevelopmental disorder.

5. Identification of the first homozygous intragenic deletion in the YY1AP1 gene in a consanguineous family: New insights into the phenotypic variability associated with Grange syndrome.

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

7. Correction: A MT-TL1 variant identified by whole exome sequencing in an individual with intellectual disability, epilepsy, and spastic tetraparesis (European Journal of Human Genetics, (2021), 29, 9, (1359-1368), 10.1038/s41431-021-00900-2)

8. Correction: Solving unsolved rare neurological diseases—a Solve-RD viewpoint (European Journal of Human Genetics, (2021), 29, 9, (1332-1336), 10.1038/s41431-021-00901-1)

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

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

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

17. De novo missense mutations in the X-linked TFE3 gene cause intellectual disability with pigmentary mosaicism and storage disorder-like features

18. Prospective interest in deploying multi-omics approaches to solve unsolved patients with suspected monogenic developmental delay syndromes

19. Linguistic characteristics of genetic primary progressive aphasias: a retrospective study of 27 cases carrying GRN and c9orf72 mutations

21. Erratum: De Novo Variants Disrupting the HX Repeat Motif of ATN1 Cause a Recognizable Non-progressive Neurocognitive Syndrome (The American Journal of Human Genetics (2019) 104(3) (542–552), (S0002929719300138), (10.1016/j.ajhg.2019.01.013))

22. De Novo Variants Disrupting the HX Repeat Motif of ATN1 Cause a Recognizable Non-Progressive Neurocognitive Syndrome

25. G.P.156

29. G.P.156: Mutations in FAM111B cause Hereditary Fibrosing Poikiloderma with tendon contracture, myopathy and pulmonary fibrosis

30. Continuous-infusion ampicillin therapy of enterococcal endocarditis in rats

31. Antagonistic effect of penicillin-amikacin combinations against enterococci

32. In vitro activity and mechanism of action of A21978C1, a novel cyclic lipopeptide antibiotic

34. Clinical, genetic, epidemiologic, evolutionary, and functional delineation of TSPEAR-related Autosomal Recessive Ectodermal Dysplasia 14

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

36. Solving patients with rare diseases through programmatic reanalysis of genome-phenome data

37. Solve-RD: systematic pan-European data sharing and collaborative analysis to solve rare diseases

38. The Phenotypic and Genotypic Spectrum of BRPF1-Related Disorder: 29 New Patients and Literature Review.

39. SMCHD1 genetic variants in type 2 facioscapulohumeral dystrophy and challenges in predicting pathogenicity and disease penetrance.

40. In-Depth Phenotyping of PIGW -Related Disease and Its Role in 17q12 Genomic Disorder.

41. A recurrent missense variant in the E3 ubiquitin ligase substrate recognition subunit FEM1B causes a rare syndromic neurodevelopmental disorder.

42. Assessment of Mendelian and risk-factor genes in Alzheimer disease: A prospective nationwide clinical utility study and recommendations for genetic screening.

43. Bi-allelic TTI1 variants cause an autosomal-recessive neurodevelopmental disorder with microcephaly.

44. The "extreme phenotype approach" applied to male breast cancer allows the identification of rare variants of ATR as potential breast cancer susceptibility alleles.

45. Bi-allelic loss-of-function variants in TMEM147 cause moderate to profound intellectual disability with facial dysmorphism and pseudo-Pelger-Huët anomaly.

46. Prenatal presentation of multiple anomalies associated with haploinsufficiency for ARID1A.

47. Hemiplegic Migraine Associated With PRRT2 Variations: A Clinical and Genetic Study.

48. [Genomic medicine].

50. Quantitative Analysis of the Potency of Equimolar Two-Drug Combinations and Combi-Molecules Involving Kinase Inhibitors In Vitro: The Concept of Balanced Targeting.

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