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1. Combining X-ray Nano-CT and XANES Techniques for 3D Operando Monitoring of Lithiation Spatial Composition evolution in NMC Electrode

2. Missense variants in ANO4 cause sporadic encephalopathic or familial epilepsy with evidence for a dominant-negative effect

4. Integrative approach to interpret DYRK1A variants, leading to a frequent neurodevelopmental disorder

5. BLOC1S5 pathogenic variants cause a new type of Hermansky–Pudlak syndrome

6. Growth charts in DYRK1A syndrome

9. CoDE-seq, an augmented whole-exome sequencing, enables the accurate detection of CNVs and mutations in Mendelian obesity and intellectual disability

10. A 600 kb deletion syndrome at 16p11.2 leads to energy imbalance and neuropsychiatric disorders.

12. Molecular diagnosis of PIK3CA-related overgrowth spectrum (PROS) in 162 patients and recommendations for genetic testing

16. Disruption of POGZ Is Associated with Intellectual Disability and Autism Spectrum Disorders

17. Growth charts in DYRK1A syndrome.

18. 19p13 microduplications encompassing NFIX are responsible for intellectual disability, short stature and small head circumference

19. 15q11.2 microdeletion (BP1–BP2) and developmental delay, behaviour issues, epilepsy and congenital heart disease: A series of 52 patients

21. 1p36 deletion syndrome: Review and mapping with further characterization of the phenotype, a new cohort of 86 patients

22. Incomplete penetrance and phenotypic variability of 6q16 deletions including SIM1

25. Morbidity and mortality from ataxia-telangiectasia are associated with ATM genotype

27. Understanding the new BRD4‐related syndrome: Clinical and genomic delineation with an international cohort study

30. Novel Pathogenic Variants in SLCO2A1 Causing Autosomal Dominant Primary Hypertrophic Osteoarthropathy

31. Cryptic genomic imbalances in de novo and inherited apparently balanced chromosomal rearrangements: Array CGH study of 47 unrelated cases

32. 1p36 deletion syndrome: Review and mapping with further characterization of the phenotype, a new cohort of 86 patients.

33. The mitochondrial solute carrier SLC25A5 at Xq24 is a novel candidate gene for non-syndromic intellectual disability

34. Neurodevelopmental phenotype in 36 new patients with 8p inverted duplication–deletion: Genotype–phenotype correlation for anomalies of the corpus callosum

35. Phenotype–genotype correlations in 17 new patients with an Xp11.23p11.22 microduplication and review of the literature

36. Reverse Phenotyping in Patients with Skin Capillary Malformations and Mosaic GNAQ or GNA11 Mutations Defines a Clinical Spectrum with Genotype-Phenotype Correlation

37. 3D Quantification Of Microstructural Properties Of Lini0.5Mn0.3Co0.2O2 High-Energy Density Electrodes By X-Ray Holographic Nano-Tomography

38. Heterogeneity of mutational mechanisms and modes of inheritance in auriculocondylar syndrome

39. EFTUD2 haploinsufficiency leads to syndromic oesophageal atresia

40. A 600 kb deletion syndrome at 16p11.2 leads to energy imbalance and neuropsychiatric disorders

41. Integrative approach to interpret DYRK1A variants, leading to a frequent neurodevelopmental disorder

42. Mirror extreme BMI phenotypes associated with gene dosage at the chromosome 16p11.2 locus

43. ARX polyalanine expansions are highly implicated in familial cases of mental retardation with infantile epilepsy and/or hand dystonia

45. Further delineation of the female phenotype withKDM5Cdisease causing variants: 19 new individuals and review of the literature

48. A Comparative Phenotypic Study of Kallmann Syndrome Patients Carrying Monoallelic and Biallelic Mutations in the Prokineticin 2 or Prokineticin Receptor 2 Genes

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