Aspectos genético-sociales de la retinosis pigmentaria
Archivo Médico de Camagüey, 2010 Fundamento: la Retinosis pigmentaria es una enfermedad de origen genético a la que se le asocian múltiples problemas sociales relacionados con su origen.
Elisa Idalmi Dyce Gordon
doaj
[Charles Darwin. The enigma of his discomfort. Did he suffer from Chagas disease?] [PDF]
Arch Cardiol Mex, 2022 Lacy Niebla MDC.
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The Negra Andaluza cattle breed has improved its status, moving from “endangered” to “threatened” thanks to the significant efforts made by breeders, universities, and governments in developing the breeding program that has been ongoing since 2012.
Delgado Bermejo, Juan Vicente +3 more
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Consanguinidad en españoles y castas de ciudad y campaña de Córdoba a fines del siglo XVIII
Revista Argentina de Antropología Biológica, 2007 A partir de datos del censo de 1795 para la provincia de Córdoba, se realizaron estimaciones de consanguinidad mediante isonimia para la Ciudad y la Campaña, tanto en “españoles” como en “castas”. Fueron calculados, en cada caso, el componente aleatorio (
Küffer, Claudio +2 more
doaj
Early-onset generalized dystonia caused by a new mutation in the KMT2B gene: Case report [PDF]
Biomedica, 2022 Rangel YA, Espinosa E.
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Estructura poblacional y consanguinidad en Dota, Costa, Rica, 1888-1962
, 2016 A study of consanguinity and population structure was carried out in a sample of 498 consanguineous (MC) and 570 non-consanguineous matings (MNC) in the Parrish of Dota, Costa Rica, during a period of 75 years. The inbreeding coefficient (F) shows fluctuations in time (476 to 194 x 10-5) with an increase from 1888 to 1917, followed by a decrease in the
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[Mitochondrial diabetes: From suspicion in primary care to a multidisciplinary family approach]. [PDF]
Aten PrimariaMacías Martínez BA +3 more
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B-cell lymphocytosis in relatives of Colombian patients with chronic B-cell lymphoproliferative disorders [PDF]
Biomedica, 2023 Celis M +4 more
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Identification of a variant in the USH1G gene in a family with Usher syndrome [PDF]
BiomedicaGélvez N, López G, Tamayo ML.
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Prenatal ultrasound diagnostic approach to Omenn syndrome: case report
Rev Colomb Obstet Ginecol, 2021 Aristizábal-Ortiz S +2 more
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