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Published in Journal of Pediatric Endocrinology & Metabolism (01.09.2014)
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Neurocognitive findings in Prader-Willi syndrome and early-onset morbid obesity
Miller, Jennifer, Kranzler, John, Liu, Yijun, Schmalfuss, Ilona, Theriaque, Douglas W., Shuster, Jonathan J., Hatfield, Ann, Mueller, O. Thomas, Goldstone, Anthony P., Sahoo, Trilochan, Beaudet, Arthur L., Driscoll, Daniel J.
Published in The Journal of pediatrics (01.08.2006)
Published in The Journal of pediatrics (01.08.2006)
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Novel human pathological mutations. Gene symbol: NR0B1. Disease: adrenal hypoplasia
Nie, Min, Fu, Yong, Lu, Lin, Mao, Jiangfeng, Chen, Zhike, Zhang, Kui, Xia, Weibo, Xing, Xiaoping, Sun, Meili, Lu, Zhaolin
Published in Human genetics (01.04.2009)
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Published in Human genetics (01.04.2009)
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Homozygosity for a dominant negative thyroid hormone receptor gene responsible for generalized resistance to thyroid hormone
Ono, S, Schwartz, I D, Mueller, O T, Root, A W, Usala, S J, Bercu, B B
Published in The journal of clinical endocrinology and metabolism (01.11.1991)
Published in The journal of clinical endocrinology and metabolism (01.11.1991)
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