Results 111 to 120 of about 20,530,783 (188)

Implementación del ADN libre circulante para la detección de aneuploidías fetales. [PDF]

Adv Lab Med
Madrigal Bajo I, Jodar Bifet M, Badenas Orquin C.   +2 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

[Diagnosis and treatment of pediatric acute lymphoblastic leukemia: Historical review]. [PDF]

Rev Med Inst Mex Seguro Soc
Valdez-Garibay B, Sosa-Bustamante GP, González AP, Linares-Segovia B, Martínez-Villegas O, Reyes-Sosa AM, Paque-Bautista C.   +6 more
europepmc   +1 more source

[A case report of severe hypocalcemia secondary to Fahr's syndrome]. [PDF]

An Sist Sanit Navar
Vallejo Ruiz M, Moral Presa I.
europepmc   +1 more source

Nutritional status in pediatric patients with predominant antibody deficiency [PDF]

Biomedica
Castaño-Jaramillo LM, Rodríguez O, Vélez-Tirado N.   +2 more
europepmc   +1 more source

Uso de inteligencia artificial en la predisposición genética a enfermedad crítica por COVID-19: evaluación comparativa de modelos de aprendizaje automático. [PDF]

Adv Lab Med
Martin Perez S, Sanchez Jimenez F, Fuentes Cantero S, Jímenez Barragan M, Sanchez Mora C, Borreguero Leon JM, Arrobas Velilla T, Valido Morales A, Delgado Torralbo JA, León-Justel A.   +9 more
europepmc   +1 more source

Clinical and genetic description of patients with chronic granulomatous disease in a pediatric hospital [PDF]

Biomedica
Berriozábal-Villarruel X, Godínez-Zamora GF, Baeza-Capetillo P, Pérez-Blanco U, Espinosa-Padilla SE, Aguirre-Hernández J, Blancas-Galicia L, Saucedo-Ramírez OJ.   +7 more
europepmc   +1 more source

First report of PURA syndrome in a Colombian patient with de novo missense variant c.692T>C (p.Phe231Ser) [PDF]

Biomedica
Cerón SM, Pérez DA, Montaño JH, Acosta MA.   +3 more
europepmc   +1 more source

[Hepatic encephalopathy from cholangitis in a young patient with ornithine transcarbamylase mutation]. [PDF]

Rev Med Inst Mex Seguro Soc
Rojas-Salazar YL, Gómez-Montañez E, Rojas-Salazar JG.   +2 more
europepmc   +1 more source