Mostrando 321 - 340 Resultados de 7,158 Para Buscar 'Tahert~', tiempo de consulta: 3.50s Limitar resultados
  1. 321
    “…Apert syndrome is autosomal dominant disease associated with multiple craniofacial and limb deformities. …”
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  2. 322
    “…Apert syndrome is a congenital craniosynostosis syndrome comprising of bilateral coronal synostosis , symmetric syndactyly of hands and feet and midface hypoplasia. …”
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  3. 323
    “…The results indicated that subjects in the high alerting efficiency group overestimated interval durations and estimated durations more accurately compared with subjects in the low alerting efficiency group. …”
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  11. 331
    por Bourgin, Patrice, Hubbard, Jeffrey
    Publicado 2016
    “…In mammals, light exerts pervasive effects on physiology and behavior in two ways: indirectly through clock synchronization and the phase adjustment of circadian rhythms, and directly through the promotion of alertness and sleep, respectively, in diurnal and nocturnal species. …”
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  14. 334
    por Samerski, Silja
    Publicado 2018
    “…Since these risks are necessarily constructed in reference to epidemiological data that postulate a statistical gaze, they also construct or make-up disembodied “individuals on alert”.…”
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  15. 335
    “…In the present study we attempted a parent–child trio, whole exome sequencing (WES) approach to study Apert's syndrome. Clinical characteristics of the child were noted down and WES was carried out using Ion Torrent System that revealed the presence of previously reported P253R mutation in FGFR2 gene. …”
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