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33 results on '"Bénédicte Demeer"'

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1. Monoallelic CRMP1 gene variants cause neurodevelopmental disorder

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

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

5. Monoallelic

6. RLIM Is a Candidate Dosage-Sensitive Gene for Individuals with Varying Duplications of Xq13, Intellectual Disability, and Distinct Facial Features

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

8. Maternal transmission ratio distortion of GNAS loss‐of‐function mutations

9. Prenatal diagnosis of femoral facial syndrome: Three case reports and literature review

10. Likely Pathogenic Variants in One Third of Non-Syndromic Discontinuous Cleft Lip and Palate Patients

11. Whole genome paired-end sequencing elucidates functional and phenotypic consequences of balanced chromosomal rearrangement in patients with developmental disorders

12. Author Correction: Postzygotic inactivating mutations of RHOA cause a mosaic neuroectodermal syndrome

13. Author response for 'Fetal phenotype of Rubinstein-Taybi syndrome caused by CREBBP mutations'

14. Fetal phenotype of Rubinstein-Taybi syndrome caused by CREBBP mutations

15. Unmasking familial CPX by WES and identification of novel clinical signs

16. Chromosomal rearrangements in the 11p15 imprinted region: 17 new 11p15.5 duplications with associated phenotypes and putative functional consequences

17. BCL11B mutations in patients affected by a neurodevelopmental disorder with reduced type 2 innate lymphoid cells

18. Whole exome sequencing identifies mutations in 10% of patients with familial non-syndromic cleft lip and/or palate in genes mutated in well-known syndromes

19. Postzygotic inactivating mutations of RHOA cause a mosaic neuroectodermal syndrome

20. A patient with Simpson-Golabi-Behmel syndrome, biliary cirrhosis and successful liver transplantation

21. Phenotypic Spectrum of Simpson-Golabi-Behmel Syndrome in a Series of 42 Cases With a Mutation in GPC 3 and Review of the Literature

22. A novel microdeletion syndrome at 9q21.13 characterised by mental retardation, speech delay, epilepsy and characteristic facial features

23. Mutations inWNT10Aare frequently involved in oligodontia associated with minor signs of ectodermal dysplasia

24. Split-hand/foot malformation with long-bone deficiency and BHLHA9 duplication: Two cases and expansion of the phenotype to radial agenesis

25. ALDH1A3 Mutations Cause Recessive Anophthalmia and Microphthalmia

26. Incomplete penetrance of biallelic ALDH1A3 mutations

27. Quelle prise en charge pour les hommes asymptomatiques, porteurs d’une mutation du gène BRCA1 ou 2 ? Résultat d’une enquête de pratique auprès des centres d’oncogénétique français

28. Clinical and molecular characterization of the 20q11.2 microdeletion syndrome: six new patients

29. Duplication 16p13.3 and the CREBBP gene: confirmation of the phenotype

30. [What management for the asymptomatic men carriers of BRCA1 or 2 mutation? Results of a survey in the French oncogenetic centers]

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

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

33. Exonic microdeletions in the X-linked PQBP1 gene in mentally retarded patients: a pathogenic mutation and in-frame deletions of uncertain effect

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