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1. CADASIL: A NOTCH3-associated cerebral small vessel disease

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3. An SCN1A gene missense variant in a Chinese Tujia ethnic family with genetic epilepsy with febrile seizures plus

4. Identification of novel compound heterozygous variants in the DNAH1 gene of a Chinese family with left-right asymmetry disorder

5. The TSC2 c.2742+5G>A variant causes variable splicing changes and clinical manifestations in a family with tuberous sclerosis complex

6. Novel compound heterozygous variants in the USH2A gene associated with autosomal recessive retinitis pigmentosa without hearing loss

7. Identification of COL4A4 variants in Chinese patients with familial hematuria

8. Human genetic basis of coronavirus disease 2019

11. Identification of DNAH17 Variants in Han-Chinese Patients With Left–Right Asymmetry Disorders

12. Novel SCN5A and GPD1L Variants Identified in Two Unrelated Han-Chinese Patients With Clinically Suspected Brugada Syndrome

13. Genetic Analysis and Literature Review of SNCA Variants in Parkinson's Disease

15. Digenic Variants in the TTN and TRAPPC11 Genes Co-segregating With a Limb-Girdle Muscular Dystrophy in a Han Chinese Family

16. DNAH11 compound heterozygous variants cause heterotaxy and congenital heart disease.

17. Novel MFSD8 Variants in a Chinese Family with Nonsyndromic Macular Dystrophy

18. Extended Study of NUS1 Gene Variants in Parkinson's Disease

19. Identification of a Novel Keratin 9 Missense Mutation in a Chinese Family with Epidermolytic Palmoplantar Keratoderma

21. Identification of a novel EVC variant in a Han‐Chinese family with Ellis‐van Creveld syndrome

22. Identification of a Heterozygous Mutation in the TGFBI Gene in a Hui-Chinese Family with Corneal Dystrophy

25. Novel MFSD8 Variants in a Chinese Family with Nonsyndromic Macular Dystrophy

27. Conformal $r$-matrix-Nijenhuis structures, symplectic-Nijenhuis structures and $\mathcal{O} N$-structures

28. Exome Sequencing of a Pedigree Reveals S339L Mutation in the TLN2 Gene as a Cause of Fifth Finger Camptodactyly.

29. Identification of a Novel Missense FBN2 Mutation in a Chinese Family with Congenital Contractural Arachnodactyly Using Exome Sequencing.

30. Identification of

31. Identification of a Novel Mutation in the COL2A1 Gene in a Chinese Family with Spondyloepiphyseal Dysplasia Congenita.

32. Novel

33. Identification of compound heterozygous DNAH11 variants in a Han-Chinese family with primary ciliary dyskinesia

34. Extending structures of lie conformal superalgebras

35. A Disease-Causing FRMD7 Variant in a Chinese Family with Infantile Nystagmus

36. Hemizygous F8 p.G201E mutation identified in a Chinese family with haemophilia A

37. Novel and Recurring NOTCH3 Mutations in Two Chinese Patients with CADASIL

38. Novel compound heterozygous mutations in the

39. 1/2-(bi)derivations and transposed Poisson algebra structures on Lie algebras.

40. DNAH11 compound heterozygous variants cause heterotaxy and congenital heart disease

41. Identification of a de novo TSC2 variant in a Han-Chinese family with tuberous sclerosis complex

42. Identification of a CCDC114 variant in a Han-Chinese patient with situs inversus

43. Extended Study of

44. The identification of a transthyretin variant p.D38G in a Chinese family with early-onset leptomeningeal amyloidosis

45. Identification of a GNE homozygous mutation in a Han‐Chinese family with GNE myopathy

46. Novel and Recurring Disease-Causing NF1 Variants in Two Chinese Families with Neurofibromatosis Type 1

47. Genetic Analysis ofLRRK1andLRRK2Variants in Essential Tremor Patients

48. Classification of finite irreducible conformal modules over a class of Lie conformal algebras of Block type

49. Association of the AADAC gene and Tourette syndrome in a Han Chinese cohort

50. A Missense Variant p.Ala117Ser in the Transthyretin Gene of a Han Chinese Family with Familial Amyloid Polyneuropathy