Molecular basis of pituitary development defects
Tunisie Medicale [La]. 2007; 85 (12): 999-1003
en Inglés
| IMEMR
| ID: emr-180199
ABSTRACT
Over the last twenty years, the progress made in molecular biology have led to the identification of many transcription factor genes, whose mutations has been reported as causes of familial hypopituitarism
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Índice:
IMEMR (Mediterraneo Oriental)
Asunto principal:
Fenotipo
/
Adenohipófisis
/
Factores de Transcripción
/
Hipopituitarismo
/
Mutación
Límite:
Humanos
Idioma:
Inglés
Revista:
Tunisie Med.
Año:
2007
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