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A novel dysfunctional LHX4 mutation with high phenotypical variability in patients with hypopituitarism. [electronic resource] by
- Castinetti, F
- Saveanu, A
- Reynaud, R
- Quentien, M H
- Buffin, A
- Brauner, R
- Kaffel, N
- Albarel, F
- Guedj, A M
- El Kholy, M
- Amin, M
- Enjalbert, A
- Barlier, A
- Brue, T
Producer: 20080821
In:
The Journal of clinical endocrinology and metabolism vol. 93
Availability: No items available.
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A nationwide study of granulosa cell tumors in pre- and postpubertal girls: missed diagnosis of endocrine manifestations worsens prognosis. [electronic resource] by
- Kalfa, N
- Patte, C
- Orbach, D
- Lecointre, C
- Pienkowski, C
- Philippe, F
- Thibault, E
- Plantaz, D
- Brauner, R
- Rubie, H
- Guedj, A M
- Ecochard, A
- Paris, F
- Jeandel, C
- Baldet, P
- Sultan, C
Producer: 20050505
In:
Journal of pediatric endocrinology & metabolism : JPEM vol. 18
Availability: No items available.
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