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145 results on '"Lynch, S.A."'

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6. Expanding the phenotype of ASXL3-related syndrome: A comprehensive description of 45 unpublished individuals with inherited and de novo pathogenic variants in ASXL3

7. A health survey of the reef forming scleractinian cold-water corals Lophelia pertusa and Madrepora oculata in a remote submarine canyon on the European continental margin, NE Atlantic

8. De novo variants in MED12 cause X-linked syndromic neurodevelopmental disorders in 18 females

11. Silicon as a model ion trap: time domain measurements of donor Rydberg states

13. The susceptibility of young prespawning oysters, Ostrea edulis, to Bonamia ostreae

16. Finding Diagnostically Useful Patterns in Quantitative Phenotypic Data

18. Clinical Presentation of a Complex Neurodevelopmental Disorder Caused by Mutations in ADNP

19. Further delineation of Pitt-Hopkins syndrome: phenotypic and genotypic description of 16 novel patients

20. Quantifying the contribution of recessive coding variation to developmental disorders

21. Heterozygous loss-of-function variants of MEIS2 cause a triad of palatal defects, congenital heart defects, and intellectual disability

22. Optimization of the high-throughput synthesis of multiblock copolymer nanoparticles in aqueous media: Via polymerization-induced self-assembly

25. Incidence and prevalence of mucopolysaccharidosis type 1 in the Irish republic

28. De novo variants in MED12cause X-linked syndromic neurodevelopmental disorders in 18 females

30. Sporadic case of fatal encephalopathy with neonatal onset associated with a T158M missense mutation in MECP2. (Case Report)

31. Large-scale discovery of novel genetic causes of developmental disorders

36. Familial neurofibromatosis microdeletion syndrome complicated by rhabdomyosarcoma. (Short Report)

40. Methionine synthase and neural tube defects

48. Towards SiGe Terahertz VCSELs

49. Electroluminescence from Si/SiGe quantum cascade emitters

50. Si/SiGe quantum-cascade emitters for terahertz applications

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