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Exclusion of the locus for autosomal recessive pseudohypoaldosteronism type 1 from the mineralocorticoid receptor gene region on human chromosome 4q by linkage analysis. [electronic resource] by
- Chung, E
- Hanukoglu, A
- Rees, M
- Thompson, R
- Dillon, M
- Hanukoglu, I
- Bistritzer, T
- Kuhnle, U
- Seckl, J
- Gardiner, R M
Producer: 19951228
In:
The Journal of clinical endocrinology and metabolism vol. 80
Availability: No items available.
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51.
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52.
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Type 1 diabetes in Jewish Ethiopian immigrants in Israel: HLA class II immunogenetics and contribution of new environment. [electronic resource] by
- Zung, A
- Elizur, M
- Weintrob, N
- Bistritzer, T
- Hanukoglu, A
- Zadik, Z
- Phillip, M
- Miller, K
- Koren, I
- Brautbar, C
- Israel, S
Producer: 20050331
In:
Human immunology vol. 65
Availability: No items available.
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53.
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Pulmonary epithelial sodium-channel dysfunction and excess airway liquid in pseudohypoaldosteronism. [electronic resource] by
- Kerem, E
- Bistritzer, T
- Hanukoglu, A
- Hofmann, T
- Zhou, Z
- Bennett, W
- MacLaughlin, E
- Barker, P
- Nash, M
- Quittell, L
- Boucher, R
- Knowles, M R
Producer: 19990715
In:
The New England journal of medicine vol. 341
Availability: No items available.
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54.
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Mutations in subunits of the epithelial sodium channel cause salt wasting with hyperkalaemic acidosis, pseudohypoaldosteronism type 1. [electronic resource] by
- Chang, S S
- Grunder, S
- Hanukoglu, A
- Rösler, A
- Mathew, P M
- Hanukoglu, I
- Schild, L
- Lu, Y
- Shimkets, R A
- Nelson-Williams, C
- Rossier, B C
- Lifton, R P
Producer: 19960325
In:
Nature genetics vol. 12
Availability: No items available.
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