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Técnico Superior Sanitario de Laboratorio de Diagnóstico Clínico March of Dimes Birth Defects Foundation American Academy of Family Physicians Atlas of Genetics and Cytogenetics in Oncology and Haematology. American College of Obstetricians and Gynecologists Wapner, R., et al. First-trimester screening for trisomies 21 and 18. New England Journal of Medicine, volumen 349, número 15, 9 de octubre de 2003, págs. 1405-1413. Ganniats TG. Justifying prenatal screening and genetic amniocentesis programs by cost effectiveness analyses: a re-evaluation. Med Decis Making 1996: 16 (1): 45-50. Asociación Catalana para el Síndrome de Prader-Willi Asociación Madrileña para el Síndrome de Prader-Willi Knudson AGJR. Mutation and cancer: Statistical study of retinoblastoma. Baena N. Guitart M. Registre de Defectes Congènits del Vallès. Hospital Parc Taulí. Sabadell. (Datos no publicados.Comunicación personal. 1999). Benacerraf BR, Frigoletto FD, Lane A, Laboda RDMS. Sonographic diagnosis of Down syndrome in the second trimester. Am J Obstet Gynecol 1985; 153:49-52. Benacerraf BR, Nadel A, Brromley B. Identification of second trimester fetuses with autosomal trisomy by the use of sonografic scoring index. Radiology 1994; 193:135-40. Benacerraf BR. Should sonographic screening for fetal Down Syndrome be applied to low risk women? Ultrasound Obstet Gynec 2000; 15:451-55. Bermejo E, Martínez Frias ML. Vigilancia epidemiológica de anomalías congénitas. Boletín del Estudio Colaborativo Español de Malformaciones Congénitas (1998). Serie 4. nº 3. Bernardino F, Cardoso R, Montenegro N, Bernardes J, de Sa JM. Semiautomated ultrasonographic measurement of fetal nuchal translucency using a computer software Fortuni Estivill A, Borrell Vilaseca A, Cortés León M, Gallo Vallejo M, González de Agüero Laborda R, González Gónzalez A, et al. Screening de cromosomopatías fetales. En: Documentos de Consenso S.E.G.O 2000; 139-77. Suárez Rodríguez MA, Ordoñez Bayón MJ. Diagnóstico prenatal. En: Brines Solanes J, Crespo Hernández M, Cruz Hernández M, Delgado Rubio A, Garagorri Otero JM, Hérnandez Rodriguez M, et al. Manual del Residente de Pediatria y sus Áreas Específicas. Guía formativa. - Salamanca Ballesteros A, Padilla Vinuesa MC, López-Jurado R. Diagnóstico prenatal de las malformaciones congénitas. Una orientación para el Médico de Familia. En: Gallo Vallejo FJ, et al. Manual del Residente de Medicina de Familia y Comuitaria. 2ª ed. Barcelona: semFYC, 1997; 973-81. U.S. Preventive Services Task Force. Guía de Medicina Clínica Preventiva. Edición Española. Barcelona: Medical Trends, 1998. Fernández Fernández I, Franch Nadal J, Martín Manzano JL, Navarro Pérez J, Orozco Beltrán D, Vázquez Garrido P. Programas Básicos de Salud. Programa del Adulto. Volumen 2. Diabetes Mellitus. Madrid: Doyma, 1998. Arribas Mir L, Bailón Muñoz E, Galvez Ibañez M, Marzo Castillejo M, Melguizo Jiménez M, Navarro Martín JA, et al. Programas Básicos de Salud. Programa de la Mujer. Volumen 1. Manejo de los problemas de salud en el embarazo. Madrid: Doyma, 2000. 303
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LABORATORIO DE GENÉTICA: GENÉTICA
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INDICE UNIDAD TEMÁTICA I. Laborato
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Presentación, normas y procedimien
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Laboratorio de Genética: Genética
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Técnico Superior Sanitario de Labo
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1. LA CÉLULA Laboratorio de Genét
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5) Diacinesis Laboratorio de Genét
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Meiosis en el sexo femenino y mascu
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UNIDAD TEMÁTICA IV GENÉTICA HERED
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