Mostrando 5,941 - 5,960 Resultados de 9,868 Para Buscar '"Arabic"', tiempo de consulta: 0.40s Limitar resultados
  1. 5941
    “…Methods: The ANGPTL8 R59W variant was genotyped in a discovery cohort of 867 Arab individuals from Kuwait. Plasma levels of ANGPTL8 and inflammatory markers were measured and tested for associations with the genotype; the associations were tested for replication in an independent cohort of 278 Arab individuals. …”
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  2. 5942
    “…METHODS: The genotypes of four VDR gene polymorphisms were determined in 253 Kuwaiti Arab T1DM patients and 214 healthy controls by PCR-RFLP analysis. …”
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  3. 5943
    “…Data was analyzed separately for the two main ethnic groups in the region, Jewish and Arab-Bedouin. RESULTS: The study cohort included 57,331 deliveries that met the inclusion criteria. …”
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  4. 5944
    “…RESULTS: The rates of anemia before delivery and in the puerperium period were similar between Jews and Arabs (before delivery: 88 (11%) versus 98 (14%); 6 weeks postpartum: 55 (21%) vs 68 (28%), respectively;p > 0.05). …”
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  5. 5945
    “…BACKGROUND: This study aimed to investigate the genetic association of specific Single Nucleotide Polymorphisms (SNPs) within the muscle segment homeobox gene 1 (MSX1) with susceptibility to the peg-shaped teeth in 36 Jordanian Arab families and case–control samples in the Jordanian Arab population. …”
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  6. 5946
  7. 5947
    “…SIMPLE SUMMARY: Bred over centuries in the Maghreb region, on a corridor between the Arab and the Western world, the North African Barb horse has been touched by many influences in the course of history. …”
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  8. 5948
    “…Accordingly, this study aims at exploring the perceptions of a diverse group of stakeholders, positioned at differing levels of the public health and education ecosystems in the United Arab Emirates, in relation to current guidelines and practices around the planning, implementation, and evaluation of school nutrition programs in Dubai, United Arab Emirates. …”
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  9. 5949
    Publicado 1987
    Libro
  10. 5950
    “…Congenital hypoparathyroidism, growth retardation and facial dysmorphism is a rare autosomal recessive disorder seen among children born to consanguineous couple of Arab ethnicity. This syndrome is commonly known as Sanjad-Sakati or hypoparathyroidism-retardation-dysmorphism syndrome (HRD). …”
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  11. 5951
  12. 5952
  13. 5953
  14. 5954
  15. 5955
  16. 5956
  17. 5957
  18. 5958
  19. 5959
  20. 5960
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