Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Mónica Quintana-Palma"'
Autor:
M.J. Zavaleta-Abreu, Mónica Aguinaga-Ríos, M.G. Echavarría-Sánchez, Patricia Grether-González, E.A. Pérez-González, Mónica Quintana-Palma, J. Castro-Llamas, M. Domínguez-Castro, P.A.T. Rodríguez-Suárez
Publikováno v:
Perinatología y Reproducción Humana, Vol 29, Iss 2, Pp 60-64 (2015)
ResumenAntecedentesLas causas genéticas más frecuentemente asociadas con infertilidad masculina son las anomalías cromosómicas y microdeleciones del cromosoma Y.ObjetivoDeterminar la frecuencia de alteraciones cromosómicas en pacientes con alter
Autor:
Emmanouil Manolakos, Loretta Thomaidis, Mónica Quintana-Palma, Druckerei Stückle, Yoichi Matsuda, Georgios S. Markopoulos, Annalisa Vetro, Chizuko Nishida, Adam J. Lukaszewski, Rosalba Sevilla-Montoya, W. Feichtinger, Claudio Oliveira, Jutta Jenderny, Nandita Barnabas, Katharina Kreskowski, Michael Schmid, Winfried Schmidt, Ioannis Papoulidis, Claus Steinlein, Monika Ziegler, Guadalupe Razo-Aguilera, Junko Ishijima, Fausto Foresti, Laura Uribe-Figueroa, Mirosław Tyrka, Adewale Adeyinka, Ricardo Utsunomia, James P. Bogart, Anja Weise, Dimitrios Noutsopoulos, Satz Mengensatzproduktion, Angeliki-Maria Vlaikou, Thomas Liehr, Maria Syrrou, Dhananjay Chitale, Priscilla Cardim Scacchetti, Sylwia Oleszczuk, José Carlos Pansonato-Alves, Lothar Kochhan, Alejandro Martínez-Juárez, Yoshinobu Uno, Jessica Sanchez
Publikováno v:
Cytogenetic and Genome Research. 142:I-IV
Autor:
Mónica Quintana-Palma, Rosalba Sevilla-Montoya, Guadalupe Razo-Aguilera, Laura Uribe-Figueroa, Alejandro Martínez-Juárez
Publikováno v:
Cytogenetic and Genome Research. 142:249-254
Pure partial trisomy 2p patients have rarely been reported. Oligonucleotide array analysis has proved to be important for examining 2p rearrangements to delineate the involved segment and to rule out additional imbalances modifying the phenotype. Her
Autor:
Susana Kofman, Verónica Fabiola Morán-Barroso, Karem Nieto-Martínez, Jaime Berumen, Ariadna Berenice Morales-Jiménez, Mónica Quintana-Palma, Fernando Fernández-Ramírez, Carolina Isabel Galaz-Montoya, Judith Villa-Morales, Alicia Cervantes, Laura Gómez-Laguna, Constanza García-Delgado
Publikováno v:
BMC Medical Genomics
Background Trisomy 1q and monosomy 3p deriving from a t(1;3) is an infrequent event. The clinical characteristics of trisomy 1q41-qter have been described but there is not a delineation of the syndrome. The 3p25.3-pter monosomy syndrome (MIM 613792)