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Autor:
Castilla, Jose A., Abellán, Fernando, Alamá, Pilar, Aura, Mónica, Bassas, Lluís, Clúa, Eli, De la Fuente, Alfonso, Guillén, Juanjo, Manau, Dolors, Rueda, Joaquin, Ruiz, Miguel, Vendrell, Xavier
Publikováno v:
In Medicina Reproductiva y Embriología Clínica January-April 2020 7(1):1-4
Autor:
Molina Romero, Marta
Publikováno v:
Digibug. Repositorio Institucional de la Universidad de Granada
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En los países desarrollados la necesidad de recurrir a técnicas de reproducción asistida con donación de gametos va en aumento debido principalmente al retraso en el deseo reproductivo. Con el aumento de la edad de la mujer existe una disminució
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https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::c353360e78f9c49d91c1fa7d1c6b80b3
http://hdl.handle.net/10481/72878
http://hdl.handle.net/10481/72878
Publikováno v:
In Revista Española de Cardiología January 2009 62(1):57-65
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In Revista Española de Cardiología (English Edition) 2009 62(1):57-65
Publikováno v:
In Obstetricia Edition: Seventh Edition. 2019:202-229
Autor:
Tetyana Korniyenko
Publikováno v:
Revista Latinoamericana de Hipertension; 2023, Vol. 18 Issue 6, p280-288, 9p
Autor:
Alonso, Joana Peñarrubia
Publikováno v:
In Lo Esencial en Medicina Reproductiva Edition: Second Edition. 2016:200-202
Akademický článek
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Cameron, M., & Moran, P. (2009). Prenatal screening ang diagnosis of neural tube defects. Prenatal Diagnosis, 29, 402–411. http://doi.org/10.1002/pd
Campbell, S. (1969). The prediction of fetal maturity by ultrasonic measurement of the biparietal diameter. The Journal of Obstetrics and Gynaecology of the British Commonwealth, 76(7), 603–609
Campbell, S. (2013). A short history of sonography in obstetrics and gynaecology. Facts, Views & Vision in ObGyn, 5(3), 213–29. Retrieved from http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=3987368&tool=pmcentrez&ren dertype=abstract
Dandona, P., Hodson, M., Bell, J., Ramdial, L., Beldon, I., & Batten, J. C. (1981). Serum immunoreactive trypsin in cystic fibrosis. Thorax, 36(1), 60–62. http://doi.org/10.1136/thx.36.1.60
Danna, K., & Nathans, D. (1971). Specific Cleavage of Simian Virus 40 DNA by Restriction Endonuclease of Hemophilus Influenzae *. Proc. Nat. Acad. Sci. USA, 68(12), 2913–2917.
Dean, L. (2005). Hemolytic disease of the newborn. In B. Beck (Ed.), Blood Groups and Red Cell Antigens (pp. 1–4).
DePristo, M. a. (2010). The $1,000 Genome: The Revolution in DNA Sequencing and the New Era of Personalized Medicine. The American Journal of Human Genetics, 87(6), 742. http://doi.org/10.1016/j.ajhg.2010.10.027
Dewey, F. E., Grove, M. E., Pan, C., Goldstein, B. A., Bernstein, J. A., Chaib, H., … Assimes, T. L. (2016). Clinical Interpretation and Implications of Whole-Genome Sequencing, 94305(10), 1035–1044. http://doi.org/10.1001/jama.2014.1717
Ding, C., Chiu, R. W. K., Lau, T. K., Leung, T. N., Chan, L. C., Chan, A. Y. Y., … Lo, Y. M. D. (2004). MS analysis of single-nucleotide differences in circulating nucleic acids: Application to noninvasive prenatal diagnosis. Proceedings of the National Academy of Sciences of the United States of America, 101(29), 10762–10767. http://doi.org/10.1073/pnas.0403962101
Dreesen, J., Destouni, A., Kourlaba, G., Degn, B., Mette, W. C., Carvalho, F., … Traeger-Synodinos, J. (2014). Evaluation of PCR-based preimplantation genetic diagnosis applied to monogenic diseases: a collaborative ESHRE PGD consortium study. European Journal of Human Genetics : EJHG, 22(8), 1012–8. http://doi.org/10.1038/ejhg.2013.277
Dussault, J. H., & Laberge, C. (1973). [Thyroxine (T4) determination by radioimmunological method in dried blood eluate: new diagnostic method of neonatal hypothyroidism?]. L’union medicale du Canada, 102(10), 2062–2064.
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Edwards, A., Hammond, H. A., Jin, L., Caskey, C. T., & Chakraborty, R. (1992). Genetic variation at five trimeric and tetrameric tandem repeat loci in four human population groups. Genomics, 12(2), 241–253. http://doi.org/10.1016/0888-7543(92)90371-X
Elger, B. S. (2010). Ethical, legal and social issues in the genetic testing of minors. Issues in clinical child psychology. http://doi.org/http://dx.doi.org/10.1007/978-1-4419-5800-6_20
Erlich, H. (2012). HLA DNA typing: Past, present, and future. Tissue Antigens, 80(1), 1–11. http://doi.org/10.1111/j.1399-0039.2012.01881.x
España, M., Benavidez, J., & Uribe, A. (2010). El rol de la creatinuria en los estudios de tamizaje para errores innatos del metabolismo: un estudio retrospectivo. Revista de La Asociacion Colombiana de Ciencias Biologicas, 22(1), 67–68.
Estrada-cuzcano, A. (2006). Uso de la técnica SSCP para detectar mutaciones puntuales del ADN mitocondrial humano. Rev. Peru. Biol., 12(3), 349–358.
Eto, K., Iwatsuki, M., Watanabe, M., Ida, S., Ishimoto, T., Iwagami, S., … Baba, H. (2014). The microRNA-21/PTEN pathway regulates the sensitivity of HER2-positive gastric cancer cells to trastuzumab. Annals of Surgical Oncology, 21(October 2013), 343–50. http://doi.org/10.1245/s10434-013-3325-7
European Society of Radiology. (2012). the Story of Radiology. International Day of Radiology, 1, 96. Retrieved from http://www.bshr.org.uk/The_Story_of_Radiology_Vol1.pdf
Evans, M., Bergum, V., Bamforth, S., & MacPhail, S. (2004). Relational ethics and genetic counseling. Nursing Ethics, 11(5), 459–471. http://doi.org/10.1191/0969733004ne724oa
Fakruddin, M., & Chowdhury, A. (2012). Pyrosequencing-an alternative to traditional Sanger sequencing. American Journal of Biochemistry and Biotechnology, 8(1), 14–20.
Fan, Y. S., Siu, V. M., Jung, J. H., & Xu, J. (2000). Sensitivity of multiple color spectral karyotyping in detecting small interchromosomal rearrangements. Genetic Testing, 4(1), 9–14. http://doi.org/10.1097/00125817-200001000-00063
Feinberg, A. P., & Tycko, B. (2004). The history of cancer epigenetics. Nature Reviews. Cancer, 4(2), 143–153. http://doi.org/10.1038/nrc1279
Feng, S., Zhou, L., Huang, C., Xie, K., & Nice, E. C. (2015). Interactomics: toward protein function and regulation. Expert Review of Proteomics, 12(1), 37–60. http://doi.org/10.1586/14789450.2015.1000870
Fernandez-Mercado, M., Manterola, L., Larrea, E., Goicoechea, I., Arestin, M., Armesto, M., … Lawrie, C. H. (2015). The circulating transcriptome as a source of non-invasive cancer biomarkers: Concepts and controversies of non-coding and coding RNA in body fluids. Journal of Cellular and Molecular Medicine, 19(10), 2307–2323. http://doi.org/10.1111/jcmm.12625
Fiorentino, F., Bono, S., Biricik, A., Nuccitelli, A., Cotroneo, E., Cottone, G., … Greco, E. (2014). Application of next-generation sequencing technology for comprehensive aneuploidy screening of blastocysts in clinical preimplantation genetic screening cycles. Human Reproduction, 29(12), 2802–2813. http://doi.org/10.1093/humrep/deu277
Fischel-Ghodsian, N. (2005). Genetic factors in aminoglycoside toxicity. Pharmacogenomics, 6, 27– 36. http://doi.org/10.1517/14622416.6.1.27
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Repositorio EdocUR-U. Rosario
Universidad del Rosario
instacron:Universidad del Rosario
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Campbell, S. (1969). The prediction of fetal maturity by ultrasonic measurement of the biparietal diameter. The Journal of Obstetrics and Gynaecology of the British Commonwealth, 76(7), 603–609
Campbell, S. (2013). A short history of sonography in obstetrics and gynaecology. Facts, Views & Vision in ObGyn, 5(3), 213–29. Retrieved from http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=3987368&tool=pmcentrez&ren dertype=abstract
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DePristo, M. a. (2010). The $1,000 Genome: The Revolution in DNA Sequencing and the New Era of Personalized Medicine. The American Journal of Human Genetics, 87(6), 742. http://doi.org/10.1016/j.ajhg.2010.10.027
Dewey, F. E., Grove, M. E., Pan, C., Goldstein, B. A., Bernstein, J. A., Chaib, H., … Assimes, T. L. (2016). Clinical Interpretation and Implications of Whole-Genome Sequencing, 94305(10), 1035–1044. http://doi.org/10.1001/jama.2014.1717
Ding, C., Chiu, R. W. K., Lau, T. K., Leung, T. N., Chan, L. C., Chan, A. Y. Y., … Lo, Y. M. D. (2004). MS analysis of single-nucleotide differences in circulating nucleic acids: Application to noninvasive prenatal diagnosis. Proceedings of the National Academy of Sciences of the United States of America, 101(29), 10762–10767. http://doi.org/10.1073/pnas.0403962101
Dreesen, J., Destouni, A., Kourlaba, G., Degn, B., Mette, W. C., Carvalho, F., … Traeger-Synodinos, J. (2014). Evaluation of PCR-based preimplantation genetic diagnosis applied to monogenic diseases: a collaborative ESHRE PGD consortium study. European Journal of Human Genetics : EJHG, 22(8), 1012–8. http://doi.org/10.1038/ejhg.2013.277
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Edwards, A., Hammond, H. A., Jin, L., Caskey, C. T., & Chakraborty, R. (1992). Genetic variation at five trimeric and tetrameric tandem repeat loci in four human population groups. Genomics, 12(2), 241–253. http://doi.org/10.1016/0888-7543(92)90371-X
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España, M., Benavidez, J., & Uribe, A. (2010). El rol de la creatinuria en los estudios de tamizaje para errores innatos del metabolismo: un estudio retrospectivo. Revista de La Asociacion Colombiana de Ciencias Biologicas, 22(1), 67–68.
Estrada-cuzcano, A. (2006). Uso de la técnica SSCP para detectar mutaciones puntuales del ADN mitocondrial humano. Rev. Peru. Biol., 12(3), 349–358.
Eto, K., Iwatsuki, M., Watanabe, M., Ida, S., Ishimoto, T., Iwagami, S., … Baba, H. (2014). The microRNA-21/PTEN pathway regulates the sensitivity of HER2-positive gastric cancer cells to trastuzumab. Annals of Surgical Oncology, 21(October 2013), 343–50. http://doi.org/10.1245/s10434-013-3325-7
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Evans, M., Bergum, V., Bamforth, S., & MacPhail, S. (2004). Relational ethics and genetic counseling. Nursing Ethics, 11(5), 459–471. http://doi.org/10.1191/0969733004ne724oa
Fakruddin, M., & Chowdhury, A. (2012). Pyrosequencing-an alternative to traditional Sanger sequencing. American Journal of Biochemistry and Biotechnology, 8(1), 14–20.
Fan, Y. S., Siu, V. M., Jung, J. H., & Xu, J. (2000). Sensitivity of multiple color spectral karyotyping in detecting small interchromosomal rearrangements. Genetic Testing, 4(1), 9–14. http://doi.org/10.1097/00125817-200001000-00063
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Feng, S., Zhou, L., Huang, C., Xie, K., & Nice, E. C. (2015). Interactomics: toward protein function and regulation. Expert Review of Proteomics, 12(1), 37–60. http://doi.org/10.1586/14789450.2015.1000870
Fernandez-Mercado, M., Manterola, L., Larrea, E., Goicoechea, I., Arestin, M., Armesto, M., … Lawrie, C. H. (2015). The circulating transcriptome as a source of non-invasive cancer biomarkers: Concepts and controversies of non-coding and coding RNA in body fluids. Journal of Cellular and Molecular Medicine, 19(10), 2307–2323. http://doi.org/10.1111/jcmm.12625
Fiorentino, F., Bono, S., Biricik, A., Nuccitelli, A., Cotroneo, E., Cottone, G., … Greco, E. (2014). Application of next-generation sequencing technology for comprehensive aneuploidy screening of blastocysts in clinical preimplantation genetic screening cycles. Human Reproduction, 29(12), 2802–2813. http://doi.org/10.1093/humrep/deu277
Fischel-Ghodsian, N. (2005). Genetic factors in aminoglycoside toxicity. Pharmacogenomics, 6, 27– 36. http://doi.org/10.1517/14622416.6.1.27
Fischer, S. G., & Lerman, L. S. (1983). DNA fragments differing by single base-pair substitutions are separated in denaturing gradient gels: Correspondence with melting theory. Proc. Nat. Acad. Sci. USA, 80, 1579–1583.
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Repositorio EdocUR-U. Rosario
Universidad del Rosario
instacron:Universidad del Rosario
El presente texto hace una recopilación cronológica de las pruebas y métodos mas utilizados para el diagnóstico y cribado de las diferentes patologías de origen genético, así como su utilización en identificación humana, se incluye informaci
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