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humans (87) 87
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familial dysalbuminemic hyperthyroxinemia (48) 48
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Clinical Chemistry, ISSN 0009-9147, 2009, Volume 55, Issue 5, pp. 1044 - 1046
  When SyD is performed in a buffer from one of the 2-step assays that yields high results for FDH samples, similarly high results are obtained (data not... 
MEDICAL LABORATORY TECHNOLOGY | Thyroxine - blood | Hyperthyroxinemia, Familial Dysalbuminemic - blood | Humans | Reagent Kits, Diagnostic | Biomedical research | Mutation | Methods | Manufacturers | Index Medicus
Journal Article
Clinical Chemistry, ISSN 0009-9147, 2011, Volume 57, Issue 3, pp. 524 - 525
Journal Article
Endocrine practice : official journal of the American College of Endocrinology and the American Association of Clinical Endocrinologists, ISSN 1530-891X, 11/2017, Volume 23, Issue 11, pp. 1325 - 1332
Journal Article
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics, ISSN 1003-9406, 02/2005, Volume 22, Issue 1, p. 40
Journal Article
Pediatrics International, ISSN 1328-8067, 05/2019, Volume 61, Issue 5, pp. 520 - 522
Journal Article
Japanese Clinical Medicine, ISSN 1179-6707, 04/2016, Volume 2016, Issue 7, p. 9
Familial dysalbuminemic hyperthyroxinemia (FDH) is a familial autosomal dominant disease caused by mutation in the albumin gene that produces a condition of... 
Case studies | Care and treatment | Gene mutations | Analysis | Hyperthyroidism | Men | ACHOO syndrome | Genetic aspects | Diagnosis | Research | Health aspects | Risk factors
Journal Article
Endocrine, ISSN 1355-008X, 12/2018, Volume 62, Issue 3, pp. 628 - 638
Journal Article
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, ISSN 0021-972X, 05/1998, Volume 83, Issue 5, pp. 1448 - 1454
Journal Article
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