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Several homozygous mutations in the gene for 11 beta-hydroxysteroid dehydrogenase type 2 in patients with apparent mineralocorticoid excess. [electronic resource] by
- Wilson, R C
- Harbison, M D
- Krozowski, Z S
- Funder, J W
- Shackleton, C H
- Hanauske-Abel, H M
- Wei, J Q
- Hertecant, J
- Moran, A
- Neiberger, R E
Producer: 19951228
In:
The Journal of clinical endocrinology and metabolism vol. 80
Availability: No items available.
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30.
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Examination of genotype and phenotype relationships in 14 patients with apparent mineralocorticoid excess. [electronic resource] by
- Dave-Sharma, S
- Wilson, R C
- Harbison, M D
- Newfield, R
- Azar, M R
- Krozowski, Z S
- Funder, J W
- Shackleton, C H
- Bradlow, H L
- Wei, J Q
- Hertecant, J
- Moran, A
- Neiberger, R E
- Balfe, J W
- Fattah, A
- Daneman, D
- Akkurt, H I
- De Santis, C
- New, M I
Producer: 19980729
In:
The Journal of clinical endocrinology and metabolism vol. 83
Availability: No items available.
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