Fragile 'X' syndrome. A case study.
Artículo
en Inglés
| IMSEAR
| ID: sea-51774
ABSTRACT
Fragile 'X' syndrome also known as the Martin-Bell syndrome or the marker 'X' syndrome is an 'X'-linked disorder with connective tissue dysplasia and varying degree of mental retardation. A case of this syndrome with characteristic Martin-Bell phenotype is presented. Oral features as yet unmentioned are added.
Texto completo:
Disponible
Índice:
IMSEAR (Asia Sudoriental)
Asunto principal:
Anomalías Dentarias
/
Humanos
/
Masculino
/
Adolescente
/
Síndrome del Cromosoma X Frágil
/
Anomalías de la Boca
Idioma:
Inglés
Año:
1996
Tipo del documento:
Artículo
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