Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Amanda F, de Figueiredo"'
Autor:
Miriam Beatriz Goulart, Eduardo Vieira Neto, Daniela R. Ney Garcia, Marília Martins Guimarães, Isaías Soares de Paiva, Karina de Ferran, Nathalia Correia Krause dos Santos, Luciana Santos Barbosa, Amanda F. de Figueiredo, Maria Cecília Menks Ribeiro, Márcia Gonçalves Ribeiro
Publikováno v:
Life, Vol 14, Iss 7, p 848 (2024)
Turner syndrome (TS) is caused by a complete or partial absence of an X or Y chromosome, including chromosomal mosaicism, affecting 1 in 2500 female live births. Sister chromatid exchange (SCE) is used as a sensitive indicator of spontaneous chromoso
Externí odkaz:
https://doaj.org/article/04226874f4d24da687ce8c5feada8d49
Autor:
Daniela R, Ney Garcia, Mariana T, de Souza, Amanda F, de Figueiredo, Moneeb A K, Othman, Katharina, Rittscher, Eliana, Abdelhay, Roberto R, Capela de Matos, Claus, Meyer, Rolf, Marschalek, Marcelo G P, Land, Thomas, Liehr, Raul C, Ribeiro, Maria Luiza Macedo, Silva
Publikováno v:
Hematological oncology. 35(4)
In pediatric acute leukemias, reciprocal chromosomal translocations frequently cause gene fusions involving the lysine (K)-specific methyltransferase 2A gene (KMT2A, also known as MLL). Specific KMT2A fusion partners are associated with the disease p
Autor:
Roberto R Capela, de Matos, Amanda F, De Figueiredo, Thomas, Liehr, Eyad, Alhourani, Mariana T, De Souza, Renata, Binato, Raul C, Ribeiro, Maria Luiza Macedo, Silva
Publikováno v:
Acta haematologica. 134(4)