Results
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10441.
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A novel nonstop mutation in the stop codon and a novel missense mutation in the type II 3beta-hydroxysteroid dehydrogenase (3beta-HSD) gene causing, respectively, nonclassic and classic 3beta-HSD deficiency congenital adrenal hyperplasia. [electronic resource] by
- Pang, Songya
- Wang, Weihua
- Rich, Barry
- David, Raphael
- Chang, Ying Tai
- Carbunaru, Goldy
- Myers, Susan E
- Howie, A Forbes
- Smillie, Karen J
- Mason, J Ian
Producer: 20020703
In:
The Journal of clinical endocrinology and metabolism vol. 87
Availability: No items available.
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10442.
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10443.
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Newly proposed hormonal criteria via genotypic proof for type II 3beta-hydroxysteroid dehydrogenase deficiency. [electronic resource] by
- Lutfallah, Chantal
- Wang, Weihua
- Mason, J Ian
- Chang, Ying Tai
- Haider, Anzar
- Rich, Barry
- Castro-Magana, Mariano
- Copeland, Kenneth C
- David, Raphael
- Pang, Songya
Producer: 20020703
In:
The Journal of clinical endocrinology and metabolism vol. 87
Availability: No items available.
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10444.
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10445.
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10446.
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10447.
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10448.
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10449.
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10450.
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10451.
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10452.
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10453.
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10454.
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10455.
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10456.
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10457.
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10458.
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10459.
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10460.
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