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Mabel Yau

Showing results (21-30 of 25) with videos related to

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Annals of the New York Academy of Sciences|August 16, 2016
A novel mutation in HSD11B2 causes apparent mineralocorticoid excess in an Omani kindredMabel Yau, Hanan Said Al Azkawi, Shozeb Haider, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|December 24, 2014
Pitfalls in hormonal diagnosis of 17-beta hydroxysteroid dehydrogenase III deficiencyAhmed Khattab, Tony Yuen, Mabel Yau, et al.
The Journal of Clinical Endocrinology and Metabolism|March 11, 2014
Noninvasive prenatal diagnosis of congenital adrenal hyperplasia using cell-free fetal DNA in maternal plasmaMaria I New, Yu K Tong, Tony Yuen, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 13, 2017
Clinical, genetic, and structural basis of apparent mineralocorticoid excess due to 11β-hydroxysteroid dehydrogenase type 2 deficiencyMabel Yau, Shozeb Haider, Ahmed Khattab, et al.
Endocrine Reviews|January 13, 2023
International Consensus Guideline on Small for Gestational Age: Etiology and Management From Infancy to Early AdulthoodAnita C S Hokken-Koelega, Manouk van der Steen, Margaret C S Boguszewski, et al.
Pageof 3

Showing results (21-30 of 25) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 25 results.
Annals of the New York Academy of Sciences|August 16, 2016
A novel mutation in HSD11B2 causes apparent mineralocorticoid excess in an Omani kindredMabel Yau, Hanan Said Al Azkawi, Shozeb Haider, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|December 24, 2014
Pitfalls in hormonal diagnosis of 17-beta hydroxysteroid dehydrogenase III deficiencyAhmed Khattab, Tony Yuen, Mabel Yau, et al.
The Journal of Clinical Endocrinology and Metabolism|March 11, 2014
Noninvasive prenatal diagnosis of congenital adrenal hyperplasia using cell-free fetal DNA in maternal plasmaMaria I New, Yu K Tong, Tony Yuen, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 13, 2017
Clinical, genetic, and structural basis of apparent mineralocorticoid excess due to 11β-hydroxysteroid dehydrogenase type 2 deficiencyMabel Yau, Shozeb Haider, Ahmed Khattab, et al.
Endocrine Reviews|January 13, 2023
International Consensus Guideline on Small for Gestational Age: Etiology and Management From Infancy to Early AdulthoodAnita C S Hokken-Koelega, Manouk van der Steen, Margaret C S Boguszewski, et al.
Pageof 3