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	1.	Current issues on molecular diagnosis of GH signaling defects. [electronic resource] by Feigerlova, Eva Hwa, Vivian Derr, Michael A Rosenfeld, Ron G Producer: 20130802 In: Endocrine development vol. 24 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	IGF-I in human growth: lessons from defects in the GH-IGF-I axis. [electronic resource] by Hwa, Vivian Fang, Peng Derr, Michael A Fiegerlova, Eva Rosenfeld, Ron G Producer: 20131024 In: Nestle Nutrition Institute workshop series vol. 71 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	A novel Y332C missense mutation in the intracellular domain of the human growth hormone receptor does not alter STAT5b signaling: redundancy of GHR intracellular tyrosines involved in STAT5b signaling. [electronic resource] by Derr, Michael A Fang, Peng Sinha, Sunil K Ten, Svetlana Hwa, Vivian Rosenfeld, Ron G Producer: 20110715 In: Hormone research in paediatrics vol. 75 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	The growth hormone receptor (GHR) c.899dupC mutation functions as a dominant negative: insights into the pathophysiology of intracellular GHR defects. [electronic resource] by Derr, Michael A Aisenberg, Javier Fang, Peng Tenenbaum-Rakover, Yardena Rosenfeld, Ron G Hwa, Vivian Producer: 20111223 In: The Journal of clinical endocrinology and metabolism vol. 96 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Severe short stature caused by novel compound heterozygous mutations of the insulin-like growth factor 1 receptor (IGF1R). [electronic resource] by Fang, Peng Cho, Yoon Hi Derr, Michael A Rosenfeld, Ron G Hwa, Vivian Cowell, Christopher T Producer: 20120409 In: The Journal of clinical endocrinology and metabolism vol. 97 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	A novel GHR intronic variant, c.266+83G>T , activates a cryptic 5' splice site causing severe GHR deficiency and classical GH insensitivity syndrome. [electronic resource] by Feigerlova, Eva Swinyard, Mike Derr, Michael A Farnsworth, Jeannie Andrew, Shayne F Rosenfeld, Ron G Hwa, Vivian Producer: 20141009 In: Hormone research in paediatrics vol. 80 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	Familial short stature caused by haploinsufficiency of the insulin-like growth factor i receptor due to nonsense-mediated messenger ribonucleic acid decay. [electronic resource] by Fang, Peng Schwartz, I David Johnson, Betty D Derr, Michael A Roberts, Charles T Hwa, Vivian Rosenfeld, Ron G Producer: 20090528 In: The Journal of clinical endocrinology and metabolism vol. 94 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	Atypical GH insensitivity syndrome and severe insulin-like growth factor-I deficiency resulting from compound heterozygous mutations of the GH receptor, including a novel frameshift mutation affecting the intracellular domain. [electronic resource] by Aisenberg, Javier Auyeung, Valerie Pedro, Helio F Sugalski, Rachel Chartoff, Amy Rothenberg, Rachel Derr, Michael A Hwa, Vivian Rosenfeld, Ron G Producer: 20110419 In: Hormone research in paediatrics vol. 74 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	Large-scale pooled next-generation sequencing of 1077 genes to identify genetic causes of short stature. [electronic resource] by Wang, Sophie R Carmichael, Heather Andrew, Shayne F Miller, Timothy C Moon, Jennifer E Derr, Michael A Hwa, Vivian Hirschhorn, Joel N Dauber, Andrew Producer: 20131104 In: The Journal of clinical endocrinology and metabolism vol. 98 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	10.	Three novel IGFALS gene mutations resulting in total ALS and severe circulating IGF-I/IGFBP-3 deficiency in children of different ethnic origins. [electronic resource] by Fofanova-Gambetti, Olga V Hwa, Vivian Kirsch, Susan Pihoker, Catherine Chiu, Harvey K Högler, Wolfgang Cohen, Laurie E Jacobsen, Christina Derr, Michael A Rosenfeld, Ron G Producer: 20090609 In: Hormone research vol. 71 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)