Mostrando 321 - 340 Resultados de 281,420 Para Buscar '"The Family"', tiempo de consulta: 1.75s Limitar resultados
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    “…In this review we discuss the different steps in the evolution of this protein family, from the formation of an ancestral fibrillar collagen gene to the formation of different clades. …”
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  4. 324
    “…The genetic architecture of loneliness was explored in an extended twin-family design including 8,683 twins, siblings and parents from 3,911 families. …”
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    “…This report describes the variable clinical features in affected individuals over two generations of a family with dentofacial deformities and review of literature.…”
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  11. 331
    “…Elastin microfibrillar interface proteins (EMILINs) and Multimerins (EMILIN1, EMILIN2, Multimerin1, and Multimerin2) constitute a four member family that in addition to the shared C-terminus gC1q domain typical of the gC1q/TNF superfamily members contain a N-terminus unique cysteine-rich EMI domain. …”
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  12. 332
    “…Familial hypercholesterolema (FH) is an inherited autosomal dominant disorder of lipid metabolism. …”
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    por Hambrecht, Martin
    Publicado 2012
    “…Young males in particular often experience their first episode while still living in their primary families. Thus, the whole family system is involved. …”
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  16. 336
    por Prajapati, Virendra Kumar
    Publicado 2013
    “…Here, we describe a case of an 8-year-old child without any family history of this genetic disorder.…”
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    por Garbacz, Pawel
    Publicado 2013
    “…Wittgenstein’s idea of family resemblance. My approach peruses the notion of frame, which was invented in cognitive psychology as an operationisable extension of this philosophical idea. …”
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  19. 339
    por Bergman, Wilma, Gruis, Nelleke A.
    Publicado 2010
    “…In this review we have aimed to focus on the clinical management of familial melanoma patients and their relatives. Along this line three major topics will be discussed: (1) management/screening of familial melanoma families: what is advised and what is the evidence thereof; (2) variability of families worldwide with regard to clinical phenotype, including cancer spectrum and likelihood of finding germline mutations and (3) background information for clinicians on the molecular biology of familial melanoma and recent developments in this field.…”
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  20. 340
    “…Its phenotypic and genotypic heterogeneity is extensive and requires careful scrutiny of its pattern of cancer associations, such as malignant melanoma associated with pancreatic cancer, in the familial atypical multiple mole melanoma syndrome, due to the CDKN2A germline mutation. …”
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