Síndrome de Turner
Palabras clave:
síndrome de Noonan, síndrome de Ullrich, monosomía X, enfermedades genéticas, (es)Descargas
Twenty wholly studied patients with turne's phenotype, whose caryologic studies confirm the chromosomal abnormality, are presented. A review of the literature on the subject has been done. Finally, a discussion on the hypothesis over the origin of the chrosomal abnormality and its significance in the various Turner's phenotypes is presented.
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