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44 results on '"Muir, Alison M."'

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1. Comprehensive EHMT1 variants analysis broadens genotype-phenotype associations and molecular mechanisms in Kleefstra syndrome

2. Rare variants in KDR, encoding VEGF Receptor 2, are associated with tetralogy of Fallot

3. Comprehensive EHMT1 variants analysis broadens genotype-phenotype associations and molecular mechanisms in Kleefstra syndrome

4. Variants in GNAI1 cause a syndrome associated with variable features including developmental delay, seizures, and hypotonia

5. NEXMIF encephalopathy: an X-linked disorder with male and female phenotypic patterns

6. TANGO2: expanding the clinical phenotype and spectrum of pathogenic variants

9. WWOX developmental and epileptic encephalopathy: Understanding the epileptology and the mortality risk

10. AMPA receptor GluA2 subunit defects are a cause of neurodevelopmental disorders

11. De novo mutations in GRIN1 cause extensive bilateral polymicrogyria

12. Biallelic ADAM22 pathogenic variants cause progressive encephalopathy and infantile-onset refractory epilepsy

13. Correction: TANGO2: expanding the clinical phenotype and spectrum of pathogenic variants

14. Biallelic ADAM22 pathogenic variants cause progressive encephalopathy and infantile-onset refractory epilepsy

15. Germline variants in tumor suppressor FBXW7 lead to impaired ubiquitination and a neurodevelopmental syndrome

16. Advanced approach for comprehensive mtDNA genome testing in mitochondrial disease

17. A recurrent, de novo pathogenic variant in ARPC4 disrupts actin filament formation and causes microcephaly and speech delay

18. Correction to: Rare variants in KDR, encoding VEGF Receptor 2, are associated with tetralogy of Fallot (Genetics in Medicine, (2021), 23, 10, (1952-1960), 10.1038/s41436-021-01212-y)

20. De novo missense variants in the E3 ubiquitin ligase adaptor KLHL20cause a developmental disorder with intellectual disability, epilepsy, and autism spectrum disorder

21. Pathogenic MAST3 variants in the STK domain are associated with epilepsy

22. FBXO28 causes developmental and epileptic encephalopathy with profound intellectual disability

23. Genetic heterogeneity in infantile spasms

24. Bi-allelic Loss-of-Function Variants in NUP188 Cause a Recognizable Syndrome Characterized by Neurologic, Ocular, and Cardiac Abnormalities

25. Pathogenic Variants in CEP85L Cause Sporadic and Familial Posterior Predominant Lissencephaly

26. ZMIZ1 Variants Cause a Syndromic Neurodevelopmental Disorder

27. AMPA receptor GluA2 subunit defects are a cause of neurodevelopmental disorders

28. Pathogenic MAST3 Variants in the STK Domain Are Associated with Epilepsy.

29. ZMIZ1 Variants Cause a Syndromic Neurodevelopmental Disorder

30. FBXO28 causes developmental and epileptic encephalopathy with profound intellectual disability.

31. Correction: TANGO2: expanding the clinical phenotype and spectrum of pathogenic variants

32. Parental Mosaicism in “De Novo” Epileptic Encephalopathies

33. GRIN2B encephalopathy : Novel findings on phenotype, variant clustering, functional consequences and treatment aspects

34. GRIN2B encephalopathy: Novel findings on phenotype, variant clustering, functional consequences and treatment aspects

35. Essential Roles of Bmp1 and Tll1 in Postnatal Root Dentin Formation

37. GRIN2Bencephalopathy: novel findings on phenotype, variant clustering, functional consequences and treatment aspects

39. AMPA receptor GluA2 subunit defects are a cause of neurodevelopmental disorders

40. De novo missense variants in the E3 ubiquitin ligase adaptor KLHL20 cause a developmental disorder with intellectual disability, epilepsy, and autism spectrum disorder.

41. A recurrent, de novo pathogenic variant in ARPC4 disrupts actin filament formation and causes microcephaly and speech delay.

42. Correction to: Rare variants in KDR, encoding VEGF Receptor 2, are associated with tetralogy of Fallot.

43. Disruptive mutations in TANC2 define a neurodevelopmental syndrome associated with psychiatric disorders.

44. GRIN2B encephalopathy: novel findings on phenotype, variant clustering, functional consequences and treatment aspects.

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