Results 71 to 80 of about 359 (93)

[20q11.2 microdeletion syndrome: a phenotypic spectrum expansion. Case report]. [PDF]

Rev Med Inst Mex Seguro Soc
Crisanto-López IE, García-González R, Saldaña-Guerrero MP, Hernández-Camacho RM, Castro-Coyotl DM.   +4 more
europepmc   +1 more source

Loss-of-function variant in MAGT1 leading to XMEN disease in a Colombian patient with a common variable immunodeficiency [PDF]

Biomedica
Gutiérrez-Hincapié S, Orrego JC, Franco JL, Trujillo-Vargas CM.   +3 more
europepmc   +1 more source

Functional characterization of two KCND3 variants associated with SCA 19/22 ataxia in Latin American families. [PDF]

Biol Res
Arancibia F, Martin F, Ruiz-Fuentes J, Diaz E, Hermosilla T, Gonzalez W, Simon F, Avila-Jaque D, Luna-Álvarez M, Dávila Ortiz de Montellano DJ, Miranda M, Bustamante ML, Varela D.   +12 more
europepmc   +1 more source

[Cancer prevention recommendations: Update 2024]. [PDF]

Aten Primaria
Bartolomé-Moreno C, Melús-Palazón E, Vela-Vallespín C, Arana-Ballestar S, Gallego M, Navarro J, Bellas-Beceiro B, Grupos de expertos del PAPPS.   +7 more
europepmc   +1 more source

[BCL11B associated disorder a case report in Mexican population. Case report]. [PDF]

Rev Med Inst Mex Seguro Soc
Crisanto-López IE, Saldaña-Guerrer MP, Hernández-Camacho RM, Castro-Coyotl DM.   +3 more
europepmc   +1 more source

[Partial trisomy 9p syndrome: Expanding the phenotype]. [PDF]

Rev Med Inst Mex Seguro Soc
Pérez-Castillo JA, Reyes-Rosales M, Cardoso-Enciso HR, Rodríguez-Cuevas JL.   +3 more
europepmc   +1 more source

Solicitud para modificar la denominación de la sección "Consejo Genético" por "Asesoramiento Genético"

Medisan, 2013
Estela Morales Peralta
doaj  

[Application of gene therapy in the treatment of hematological diseases: achievements, and economic and ethical aspects of the topic]. [PDF]

Rev Med Inst Mex Seguro Soc
Diaz-Garcia H, Moran-Espinosa MC, Sánchez-Urbina R.   +2 more
europepmc   +1 more source