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  1. 1681
    por Crellin, J K
    Publicado 1971
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    William Cullen: his calibre as a teacher, and an unpublished introduction to his A Treatise of the Materia Medica, London, 1773.
  2. 1682
    por Burnby, J G L
    Publicado 1995
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    The medical casebook of William Brownrigg, M.D., F.R.S., (1712–1800) of the town of Whitehaven in Cumberland, Medical History
  3. 1683
    por Wilde, C. B.
    Publicado 1982
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    “The Earth generated and anatomized” by William Hobbs. An early eighteenth-century theory of the earth, (Bulletin of the British Museum (Natural History)
  4. 1684
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    William Beaumont's Letter to His New Haven Bookseller, Hezekiah Howe, With a Bibliographical Description of the Editions of Beaumont's Book
  5. 1685
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    The Giant Cretaceous Coelacanth (Actinistia, Sarcopterygii) Megalocoelacanthus dobiei Schwimmer, Stewart & Williams, 1994, and Its Bearing on Latimerioidei Interrelationships
  6. 1686
    “…Harlequin Ducks (Histrionicus histrionicus) were adversely affected by the Exxon Valdez oil spill (EVOS) in Prince William Sound (PWS), Alaska, and some have suggested effects continue two decades later. …”
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    Quantitative Assessment of Current Risks to Harlequin Ducks in Prince William Sound, Alaska, from the Exxon Valdez Oil Spill
  7. 1687
    por Hogan, Andrew J.
    Publicado 2014
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    The ‘Morbid Anatomy’ of the Human Genome: Tracing the Observational and Representational Approaches of Postwar Genetics and Biomedicine The William Bynum Prize Essay
  8. 1688
    por Crespi, Bernard J, Hurd, Peter L
    Publicado 2014
    “…Deletions and duplications of the Williams-syndrome region have also been associated with autism, and with schizophrenia, two disorders centrally involving social cognition. …”
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    Cognitive-behavioral phenotypes of Williams syndrome are associated with genetic variation in the GTF2I gene, in a healthy population
  9. 1689
    “…The phenotype of Src (thl/thl) mice showed significant overlap with Williams-Beuren syndrome (WBS), a disorder caused by the deletion of several genes, including General Transcription Factor 2-I (GTF2I). …”
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    Disruption of Src Is Associated with Phenotypes Related to Williams-Beuren Syndrome and Altered Cellular Localization of TFII-I1,2
  10. 1690
    “…The Williams-Beuren syndrome is a rare genetic disease. …”
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    Malformations vasculaires au cours du syndrome de Williams-Beuren: à propos de trois nouvelles observations
  11. 1691
    “…BACKGROUND: Williams-Beuren Syndrome (WBS) is a rare neurodevelopmental disorder characterized by dysmorphic features, cardiovascular defects, cognitive deficits and developmental delay. …”
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    Genome wide array-CGH and qPCR analysis for the identification of genome defects in Williams’ syndrome patients in Saudi Arabia
  12. 1692
    “…The aims of this study were to: provide a precise characterisation of spatial category representations in Williams syndrome (WS); to determine the nature of the mechanistic contributions from spatial language performance and non-verbal cognition to spatial category representations in WS; and to explore the stability of spatial category representations in WS using error analysis. …”
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    Impaired Spatial Category Representations in Williams Syndrome; an Investigation of the Mechanistic Contributions of Non-verbal Cognition and Spatial Language Performance
  13. 1693
    “…Williams syndrome (7q11.23 microdeletion) is characterized by specific alterations in neurocognitive architecture and functioning, as well as disordered sleep. …”
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    Increased overall cortical connectivity with syndrome specific local decreases suggested by atypical sleep-EEG synchronization in Williams syndrome
  14. 1694
    por Jones, Thos.
    Publicado 1801
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    Case of Mr. William Windsor, of Bettesfield, in the Parish of Harweir, and County of Flint, a Farmer's Son, Ten Years of Age
  15. 1695
    “…We then evaluate the Hebb–Williams maze paradigm (Hebb and Williams, 1946; Rabinovitch and Rosvold, 1951) on the basis of these criteria using Fragile X syndrome (FXS) as model disease. …”
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    Utility of the Hebb–Williams Maze Paradigm for Translational Research in Fragile X Syndrome: A Direct Comparison of Mice and Humans
  16. 1696
    Publicado 1851
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    Some Account of the Life and Scientific Writings of William Prout, M.D., F.R.S., Fellow of the College of Physicians, London
  17. 1697
    por Dolscheid, Sarah, Penke, Martina
    Publicado 2018
    “…In order to determine the specific contributions of linguistic and number skills in quantifier comprehension, we examined two groups of participants that differ in their language abilities while their number skills appear to be similar: Participants with Down syndrome (DS) and participants with Williams syndrome (WS). Compared to rather poor linguistic skills of individuals with DS, individuals with WS display relatively advanced language abilities. …”
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    Quantifier comprehension is linked to linguistic rather than to numerical skills. Evidence from children with Down syndrome and Williams syndrome
  18. 1698
    “…Rimicaris chacei Williams and Rona 1986, formerly named as Chorocaris chacei, is a caridean shrimp living in deep-sea hydrothermal ecosystems. …”
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    Gill chamber and gut microbial communities of the hydrothermal shrimp Rimicaris chacei Williams and Rona 1986: A possible symbiosis
  19. 1699
    “…ABSTRACT: Williams-Beuren syndrome (WBS) (OMIM 194050) is caused by interstitial deletions or duplications of the 7q11.23 chromosomal region and characterised through a complex phenotype. …”
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    Array CGH - A Powerful Tool in Molecular Diagnostic of Pathogenic Microdeletions - Williams-Beuren Syndrome - A Case Report
  20. 1700
    “…BACKGROUND: Insufficient elastin synthesis leads to vascular complications and arterial hypertension in children with Williams-Beuren syndrome. Restoring sufficient quantity of elastin should then result in prevention or inhibition of vascular malformations and improvement in arterial blood pressure. …”
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    Minoxidil versus placebo in the treatment of arterial wall hypertrophy in children with Williams Beuren Syndrome: a randomized controlled trial
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