Search

Your search keyword '"Mignot, C."' showing total 12 results

Search Constraints

Start Over You searched for: Author "Mignot, C." Remove constraint Author: "Mignot, C." Language undetermined Remove constraint Language: undetermined
12 results on '"Mignot, C."'

Search Results

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

2. Effects of eight neuropsychiatric copy number variants on human brain structure

3. Additional file 2 of SATB2-associated syndrome: characterization of skeletal features and of bone fragility in a prospective cohort of 19 patients

4. Additional file 1 of SATB2-associated syndrome: characterization of skeletal features and of bone fragility in a prospective cohort of 19 patients

6. Defining the Effect of the 16p11.2 Duplication on Cognition, Behavior, and Medical Comorbidities

7. Optical neuromyelitis of Devic and patients of high risk: retrospective national inquiry

8. Neuromyelitis optica in France: a multicentre retrospective study of 125 patients meeting the 2006 criteria

9. Neuromyelitis optica in a paediatric population

10. Recurrent de novo missense variants in GNB2 can cause syndromic intellectual disability

11. The epileptology of GNB5 encephalopathy

12. NovelKCNQ2andKCNQ3Mutations in a Large Cohort of Families with Benign Neonatal Epilepsy: First Evidence for an Altered Channel Regulation by Syntaxin-1A

Catalog

Books, media, physical & digital resources