Buscar
Mostrando ítems 1-10 de 638
Biosocial correlates and spatial distribution of consanguinity in South America
(Wiley-liss, Div John Wiley & Sons Inc, 2016-05)
Objective: To analyze potential biosocial factors in consanguineous unions according to the level of consanguinity and its spatial distribution in South America. Methods: The data used came from the Latin American Collaborative ...
Overdenture as a restorative option for hypocalcified-hypoplastic amelogenesis imperfecta: a case report.
(2009-08-06)
AIM: The aim of this report is to describe the restorative treatment of an 18-year-old patient diagnosed with autosomal recessive hypocalcified-hypoplastic amelogenesis imperfecta (AI). BACKGROUND: Esthetic and functional ...
Is the Central Valley of Costa Rica a genetic isolate?
(Universidad de Costa Rica, 2004)
Early detection of leprosy by examination of household contacts, determination of serum anti-PGL-1 antibodies and consanguinity
(Instituto Oswaldo Cruz, Ministério da Saúde, 2011)
A cross-sectional clinical trial in which the serum anti-phenolic glycolipid (anti-PGL-1) antibodies were analysed in household contacts (HHC) of patients with leprosy as an adjunct early leprosy diagnostic marker was ...
Consanguinity by random isonymy and socioeconomic development in Argentina: a population study
(Cambridge University Press, 2016-10)
In human populations various flexible, labile and interdependent structures (genetic, demographic, socioeconomic) co-exist, each of which can be organized in an hierarchical order corresponding to administrative entities. ...
NEWLY RECOGNIZED AUTOSOMAL RECESSIVE FACIOTHORACOSKELETAL SYNDROME
(Wiley-Blackwell, 1994-01-15)
We report on 2 brothers, born to consanguineous parents presenting thin/long face, small ears, blepharophimosis, malar hypoplasia, long neck, pectus excavatum, brachy-camptodactyly, and sacral dimple. We suspect that these ...
NEWLY RECOGNIZED AUTOSOMAL RECESSIVE FACIOTHORACOSKELETAL SYNDROME
(Wiley-Blackwell, 1994-01-15)
We report on 2 brothers, born to consanguineous parents presenting thin/long face, small ears, blepharophimosis, malar hypoplasia, long neck, pectus excavatum, brachy-camptodactyly, and sacral dimple. We suspect that these ...