Correspondence
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Open Access
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Correspondence
| Open AccessMolecular genetic testing of congenital adrenal hyperplasia due to 21-hydroxylase deficiency should include CAH-X chimeras
- Qizong Lao
- & Deborah P. Merke
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Policy
| Open AccessEMQN best practice guidelines for molecular genetic testing and reporting of 21-hydroxylase deficiency
- Sabina Baumgartner-Parzer
- , Martina Witsch-Baumgartner
- & Wolfgang Hoeppner
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A unique haplotype of RCCX copy number variation: from the clinics of congenital adrenal hyperplasia to evolutionary genetics
- Márton Doleschall
- , Andrea Luczay
- & Attila Patócs
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Congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency: functional consequences of four CYP11B1 mutations
- Soara Menabò
- , Seher Polat
- & Felix G Riepe