Results 11 to 20 of about 63,159 (270)

Genetica y libertad

Pensamiento Jurídico, 1995
Genetica y ...
Bernanrd Edelman
doaj   +1 more source

Genetica y derecho penal

Pensamiento Jurídico, 1995
Genetica y derecho ...
Antonio Jose Cancino Moreno
doaj   +1 more source

Victimologia y Genetica

Pensamiento Jurídico, 1995
Victimologia y ...
Abelardo Rivera Llano
doaj   +2 more sources

Correction: CancerHubs data Explorer: a web application for investigating mutation-enriched protein interaction hubs in human cancers [PDF]

BioData Mining
Ivan Ferrari, Elisa Arsuffi, Stefano Biffo, Nicola Manfrini   +3 more
doaj   +2 more sources

Determinanten van ziekte en gezondheid op hoge leeftijd: Nieuwe inzichten uit de Leidse verouderingsstudies

Tijdschrift voor Gerontologie en Geriatrie, 2023
Het klinisch wetenschappelijk onderzoek van de afdeling Ouderengeneeskunde van het Leids Universitair Medisch Centrum is gericht op de ontrafeling van de oorzaken van ziekte en gezondheid op hoge leeftijd.
A.J.M. de Craen, A.M. Oleksik, A.B. Maier, R.G.J. Westendorp   +3 more
doaj   +1 more source

European guidelines from the EHTG and ESCP for Lynch syndrome: an updated third edition of the Mallorca guidelines based on gene and gender

BJS (British Journal of Surgery), EarlyView., 2020
Recommendations for clinical and molecular identification of LS, surgical and endoscopic management of LS‐associated colorectal cancer and preventive measures for cancer were produced. The emphasis was on surgical and gastroenterological aspects of the cancer spectrum.
T. T. Seppälä, A. Latchford, I. Negoi, A. Sampaio Soares, R. Jimenez‐Rodriguez, L. Sánchez‐Guillén, D. G. Evans, N. Ryan, E. J. Crosbie, M. Dominguez‐Valentin, J. Burn, M. Kloor, M. von Knebel Doeberitz, F. J. B. van Duijnhoven, P. Quirke, J. R. Sampson, P. Møller, G. Möslein, on behalf of the European Hereditary Tumour Group (EHTG) and European Society of Coloproctology (ESCP)   +18 more
wiley   +1 more source

Wilson's disease in Southern Brazil: genotype-phenotype correlation and description of two novel mutations in ATP7B gene

Arquivos de Neuro-Psiquiatria, 2013
OBJECTIVE: Wilson's disease (WD) is an inborn error of metabolism caused by abnormalities of the copper-transporting protein encoding gene ATP7B.
Ricardo Schmitt de Bem, Salmo Raskin, Dominique Araujo Muzzillo, Marta Mitiko Deguti, Eduardo Luiz Rachid Cancado, Thiago Ferreira Araujo, Maria Cristina Nakhle, Egberto Reis Barbosa, Renato Puppi Munhoz, Helio Afonso Ghizoni Teive   +9 more
doaj   +1 more source

Familial adult spinal muscular atrophy associated with the VAPB gene: report of 42 cases in Brazil

Arquivos de Neuro-Psiquiatria, 2013
Familial spinal muscular atrophy (FSMA) associated with the vesicle-associated membrane protein-associated protein B (VAPB) gene is a rare autosomal dominant disease with late onset and slow progression.
Victor Kosac, Marcos R. G. de Freitas, Frederico M. Prado, Osvaldo J. M. Nascimento, Caroline Bittar   +4 more
doaj   +1 more source

Genetica Humana

European Journal of Histochemistry, 2015
Sometimes we do not realize that Spanish speaking people are one of the major linguistic group on our planet! Thus we have to welcome this excellent book devoted to, as the title clearly tell us, human genetics for the pleasure of the Spanish speaking ...
CarloAlberto Redi
doaj   +1 more source

Sobre-genética

Entretextos, 2013
Compartimos al lector un panorama de cómo han ido cambiando los métodos de identificación de acuerdo con las características de los organismos a lo largo de la historia de la humanidad, de tal manera que ahora con la epigenética podemos distinguir una ...
Marcela Angélica De la Fuente Hernández , Jorge Ángel Marcos Viquez , Mauricio Adrián Orozco Mena , José Osman Franco Gallardo   +3 more
doaj   +1 more source