Results 51 to 60 of about 97 (69)
Justificación y objetivo: el síndrome del cromosoma X frágil es la principal causa de retardo mental hereditario. Afecta a 1:4 000 varones y a 1:6 000 mujeres.
Patricia Cuenca-Berger +2 more
doaj
La enfermedad de Pelizaeus Merzbacher es una entidad que consiste en leucodistrofia lentamente progresiva, clínicamente heterogénea, con un espectro dado desde la infancia.
T. Castro +3 more
doaj
22q11.2 deletion detected by in situ hybridization in Mexican patients with velocardiofacial syndrome-like features. [PDF]
Ramírez-Velazco A +5 more
europepmc +1 more source
Mosaic trisomy 8 detected by fibroblasts cultured of skin. [PDF]
Giraldo G +4 more
europepmc +1 more source
[Inequalities in time to diagnosis of Down Syndrome in Bolivia]. [PDF]
Linares Terrazas D +2 more
europepmc +1 more source
[Rare diseases in a medical genetics service of population with social security]. [PDF]
Jiménez-Pérez B +6 more
europepmc +1 more source
Gestational, perinatal and family findings of patients with Patau syndrome. [PDF]
Rosa RF +8 more
europepmc +1 more source
Mexican position paper for the diagnosis and treatment of cardiac amyloidosis. [PDF]
Berrios-Bárcenas EA +21 more
europepmc +1 more source
[Medical genetics services in VenezuelaServiços de genética médica na Venezuela].
Torre-Hernandez CA +4 more
europepmc +1 more source

