Browsing by Author Gutiérrez Angulo, Melva

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Issue DateTitleAuthor(s)
Sep-201246,XX ovotesticular disorder in a Mexican patient with Beckwith–Wiedemann syndrome: a case report.Macías Gómez, Nelly Margarita; Leal Ugarte, Evelia; Gutiérrez Angulo, Melva; Domínguez Quezada, Guadalupe; Rivera, Horacio; Barros Núñez, Patricio
25-Jul-2002A 45,X sterile male with Yp disguised as 21pDávalos Rodríguez, Ingrid P.; Rivera, Horacio; Vásquez, Ana I.; Gutiérrez Angulo, Melva; Hernández Váquez, Martha C.; Cortina Luna, Fidel A.; Wong Ley, Luis E.; Domínguez Quezada, María G.
Mar-2005A complex translocation (9;22;16)(q34;q11.2;p13) in chronic myelocytic leukemia.Meza Espinoza, Juan Pablo; Picos Cárdenas, Verónica Judith; Vásquez Jiménez, Erika Alejandra; Gutiérrez Angulo, Melva; Esparza Flores, María Amparo; González García, Juan Ramón
2007A de novo interstitial 6q deletion in a boy with a split hand malformationDurán González, Jorge; Gutiérrez Angulo, Melva; García Cruz, Diana; Ayala Madrigal, María de la Luz; Padilla, Miguel; Dávalos, Ingrid P.
Sep-2017A survey of the clinicopathological and molecular characteristics of patients with suspected Lynch syndrome in Latin AmericaRossi, Benedito Mauro; Palmero, Edenir Inêz; López-Kostner, Francisco; Sarroca, Carlos; Vaccaro, Carlos Alberto; Spirandelli, Florencia; Ashton-Prolla, Patricia; Rodriguez, Yenni; de Campos Reis Galvão, Henrique; Reis, Rui Manuel; Escremim de Paula, André; Capochin Romagnolo, Luis Gustavo; Alvarez, Karin; Della Valle, Adriana; Neffa, Florencia; Kalfayan, Pablo German; Spirandelli, Enrique; Chialina, Sergio; Gutiérrez Angulo, Melva; Castro-Mujica, Maria del Carmen; Sanchez de Monte, Julio; Quispe, Richard; da Silva, Sabrina Daniela; Rossi, Norma Teresa; Barletta-Carrillo, Claudia; Revollo, Susana; Taborga, Ximena; Morillas, L. Lena; Tubeuf, Hélène; Monteiro-Santos, Erika Maria; Piñero, Tamara Alejandra; Dominguez-Barrera, Constantino; Wernhoff, Patrik; Martins, Alexandra; Hovig, Eivind; Møller, Pål; Dominguez-Valentin, Mev
2004A t(1;9)(q23.3~q25;q34) affecting the ABL1 gene in a biphenotypic leukemia.González García, Juan Ramón; Bohlander, Stefan K.; Gutiérrez Angulo, Melva; Esparza Flores, María Amparo; Picos Cárdenas, Verónica Judith; Meza Espinoza, Juan Pablo; Ayala Madrigal, María de la Luz; Rivera, Horacio
18-Mar-2019ADIPOQ rs2241766 SNP as protective marker against DIBC development in Mexican populationMacías Gómez, Nelly Margarita; Hernández Terrones, María Carmen; Ramírez Guerrero, Angélica Araceli; Leal Ugarte, Evelia; Gutiérrez Angulo, Melva; Peregrina Sandoval, Jorge
18-Mar-2019ADIPOQ rs2241766 SNP as protective marker against DIBC development in Mexican population.Macías Gómez, Nelly Margarita; Hernández Terrones, María Carmen; Ramírez Guerrero, Angélica Araceli; Leal Ugarte, Evelia; Gutiérrez Angulo, Melva; Peregrina Sandoval, Jorge
Mar-1999An extra idic(21)(q22.1) in a child with some features of Down’s syndromeGutiérrez Angulo, Melva; Ramos, Al; Dávalos, Nory O.; Sánchez Corona, José; Rivera, Horacio
2010Association of LEP and ADIPOQ common variants with colorectal cancer in Mexican patients.Partida Pérez, Miriam; Ayala Madrigal, María  de la Luz; Peregrina Sandoval, Jorge; Macías Gómez, Nelly; Moreno Ortiz, José;  Leal Ugarte, Evelia; Cárdenas Meza, Mario; Centeno Flores, Manuel; Maciel Gutiérrez, Víctor; Cabrales, Enrique; Cervantes Ortiz, Sergio; Gutiérrez Angulo, Melva
Oct-2012Association of serotonin transporter gene polymorphism 5-HTTLPR and depressive disorder in a Mexican populationPeralta Leal, Valeria; Leal Ugarte, Evelia; Meza Espinoza, Juan Pablo; Gutiérrez Angulo, Melva; Hernández Benítez, Catalina T.; García Rodríguez, Alfonso; Dávalos Rodríguez, Ingrid P.; Gonzales, Enrique; Durán González, Jorge
Oct-2018Association of the SLC6A4 gene 5HTTLPR polymorphism and ADHD with epilepsy, gestational diabetes, and parental substance abuse in Mexican mestizo childrenDurán González, Jorge; Leal Ugarte, Evelia; Cruz Alcalá, Leonardo Eleazar; Gutiérrez Angulo, Melva; Gallegos Arreola, Martha Patricia; Meza Espinoza, Juan Pablo; Reyes Zurita, Itzayana; Padilla Macías, Patricia Lizbeth; Cruz Martín del Campo, Edgar; Peralta Leal, Valeria
Dec-2006Cardio-facio-cutaneous syndrome with hemihidrosis: ectodermal dysplasias spectrum?Leal Ugarte, Evelia; Macías Gómez, Nelly Margarita; Gutiérrez Angulo, Melva; Barros Núñez, Patricio
Aug-1999Chromosome 9qh inversions may not be true inversionsRivera, Horacio; Gutiérrez Angulo, Melva; González García, Juan Ramón
2002del(X)(p22.1)/r(X)(p22.1q28) dynamic mosaicism in a Turner syndrome patientGutiérrez Angulo, Melva; Lazalde, Brissia; Vásquez, Ana I.; Leal, Caridad; Corral, Elisa; Rivera, Horacio
Sep-2004Increased expression of AML1-a and acquired chromosomal abnormalities in childhood acute lymphoblastic leukemiaGutiérrez Angulo, Melva; González García, Juan Ramón; Meza Espinoza, Juan Pablo; Picos Cárdenas, V.J.; Esparza Flores, M.A.; López Guido, B.; Rivera, Horacio
2003Isodicentric Y chromosomes and secondary microchromosomes.Rivera, Horacio; Ayala Madrigal, Laura Margarita; Gutiérrez Angulo, Melva; Vasquez, Al; Ramos, AL
2008MDR1 C3435T Polymorphism in Mexican Children with Acute Lymphoblastic Leukemia and in Healthy Individuals.Leal Ugarte, Evelia; Gutiérrez Angulo, Melva; Macías Gómez, Nelly M.; Peralta Leal, Valeria
Jun-2012MLH1 and XRCC1 polymorphisms in Mexican patients with colorectal cancerMuñiz Mendoza, R.; Ayala Madrigal, María de la Luz; Partida Pérez, M.; Peregrina Sandoval, J.; Leal Ugarte, E.; Macías Gómez, Nelly; Peralta Leal, Valeria; Meza Espinoza, Juan Pablo; Moreno Ortiz, J.M.; Ramírez Ramírez, R.; Suárez Villanueva, S.; Gutiérrez Angulo, Melva
Nov-2008Molecular Characterization of a Patient With 3p Deletion Syndrome and a Review of the LiteratureFernandez, Thomas V.; García González, I.J.; Mason, Christopher E.; Hernández Zaragoza, G.; Ledezma Rodríguez, V.C.; Anguiano Alvarez, V.M.; E’Vega, R.; Gutiérrez Angulo, Melva; Maya, M.L.; García Bejarano, H.E.; González Cruz, M.; Barrios, S.; Atorga, R.; López Cardona, M.G.; Armendariz Borunda, J.; State, Matthew W.; Dávalos, Nory O.