Fingerprint
Dive into the research topics of 'First trimester prenatal treatment and molecular genetic diagnosis of congenital adrenal hyperplasia (21-hydroxylase deficiency)'. Together they form a unique fingerprint.- Sort by
- Weight
- Alphabetically
P. W. Speiser, N. Laforgia, K. Kato, J. Pareira, R. Khan, S. Y. Yang, C. Whorwood, P. C. White, S. Elias, E. Schriock, E. Schriock, J. L. Simpson, M. Taslimi, J. Najjar, S. May, G. Mills, C. Crawford, M. I. New
Research output: Contribution to journal › Article › peer-review