Bálint syndrome in a patient with drug-resistant epilepsy having underlying X-linked lissencephaly with subcortical band heterotopia/"double cortex" syndrome. [PDF]
Ghosh R +5 more
europepmc +1 more source
[Doctor, I have a lump on the palate]. [PDF]
Mozo Puebla MÁ, Morales Puebla JM.
europepmc +1 more source
Prognostic significance of telomerase reverse transcriptase promoter gen mutations in high grade meningiomas [PDF]
Cañas A +31 more
europepmc +1 more source
Métodos experimentales para el estudio de los genomas [PDF]
González-Siso, María-Isabel +1 more
core
First report of PURA syndrome in a Colombian patient with de novo missense variant c.692T>C (p.Phe231Ser) [PDF]
Cerón SM +3 more
europepmc +1 more source
Adult-onset cerebral X-linked adrenoleukodystrophy presenting with frontal lobe syndrome caused by a de novo <i>ABCD1</i> gene mutation (c.1415_1416delAG, p.Gln472fs*83). [PDF]
Ghosh R +4 more
europepmc +1 more source
[Dilated cardiomyopathy and conduction disorder due to <i>TNNI3K</i> mutation]. [PDF]
Gayán-Ordás J +5 more
europepmc +1 more source
Identificación genética de restos humanos quemados en un caso de desastre vehicular.
Objetivos: Identificar restos quemados en un caso de desastre vehicular ocurrido en la carretera Desaguadero, La Paz, Bolivia. Introducción: La identificación genética de restos quemados (tejidos, huesos o dientes) representa un reto debido a que el ADN
Karina Salazar Chávez +4 more
doaj
[Solitary dorsal paravertebral tumor: radiological and histopathological characterization of a pediatric case of nodular fasciitis]. [PDF]
Arredondo Montero J +4 more
europepmc +1 more source
Case report of heterotaxy syndrome with sinus node dysfunction and left ventricular hypertrabeculation: clinical and genetic insights. [PDF]
Matta MG +6 more
europepmc +1 more source

