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2013 | 1 |
2015 | 1 |
2024 | 0 |
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A shared genetic basis for self-limited delayed puberty and idiopathic hypogonadotropic hypogonadism.
J Clin Endocrinol Metab. 2015 Apr;100(4):E646-54. doi: 10.1210/jc.2015-1080. Epub 2015 Jan 30.
J Clin Endocrinol Metab. 2015.
PMID: 25636053
Free PMC article.
Common and rare von Willebrand factor (VWF) coding variants, VWF levels, and factor VIII levels in African Americans: the NHLBI Exome Sequencing Project.
Johnsen JM, Auer PL, Morrison AC, Jiao S, Wei P, Haessler J, Fox K, McGee SR, Smith JD, Carlson CS, Smith N, Boerwinkle E, Kooperberg C, Nickerson DA, Rich SS, Green D, Peters U, Cushman M, Reiner AP; NHLBI Exome Sequencing Project.
Johnsen JM, et al.
Blood. 2013 Jul 25;122(4):590-7. doi: 10.1182/blood-2013-02-485094. Epub 2013 May 20.
Blood. 2013.
PMID: 23690449
Free PMC article.
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