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	1.	Newborn screening for congenital adrenal hyperplasia. [electronic resource] by Pang, Songya Producer: 20040114 In: Pediatric annals vol. 32 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Extra-adrenal induction of Cyp21a1 ameliorates systemic steroid metabolism in a mouse model of congenital adrenal hyperplasia. [electronic resource] by Naiki, Yasuhiro Miyado, Mami Horikawa, Reiko Katsumata, Noriyuki Onodera, Masafumi Pang, Songya Ogata, Tsutomu Fukami, Maki Producer: 20170217 In: Endocrine journal vol. 63 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Carriers for type II 3beta-hydroxysteroid dehydrogenase (HSD3B2) deficiency can only be identified by HSD3B2 genotype study and not by hormone test. [electronic resource] by Pang, Songya Carbunaru, Goldy Haider, Anzar Copeland, Kenneth C Chang, Ying Tai Lutfallah, Chantal Mason, J Ian Producer: 20030530 In: Clinical endocrinology vol. 58 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	The hormonal phenotype of Nonclassic 3 beta-hydroxysteroid dehydrogenase (HSD3B) deficiency in hyperandrogenic females is associated with insulin-resistant polycystic ovary syndrome and is not a variant of inherited HSD3B2 deficiency. [electronic resource] by Carbunaru, Goldy Prasad, Pallavi Scoccia, Bert Shea, Patrick Hopwood, Nancy Ziai, Fuad Chang, Ying Tai Myers, Susan E Mason, J Ian Pang, Songya Producer: 20040326 In: The Journal of clinical endocrinology and metabolism vol. 89 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	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 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	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 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)