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Ferraz-de-Souza B, Achermann JC 
Disorders of adrenal development. [Journal Article]
Endocr Dev 2008.:19-32.
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Lin L, Ferraz-de-Souza B, Achermann JC 
Genetic disorders involving adrenal development. [Journal Article]
Endocr Dev 2007.:36-46.
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Lin L, Hindmarsh PC, Metherell LA, et al. 
Severe loss-of-function mutations in the adrenocorticotropin receptor (ACTHR, MC2R) can be found in patients diagnosed with salt-losing adrenal hypoplasia. [Journal Article]
Clin Endocrinol (Oxf) 2007 Feb; 66(2):205-10.
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Kempná P, Flück CE 
Adrenal gland development and defects. [JOURNAL ARTICLE]
Best Pract Res Clin Endocrinol Metab 2008 Feb; 22(1):77-93.
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Achermann JC, Meeks JJ, Jameson JL 
Phenotypic spectrum of mutations in DAX-1 and SF-1. [Journal Article, Review]
Mol Cell Endocrinol 2001 Dec 20; 185(1-2):17-25.
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Tsai WY, Tung YC 
Novel deletion mutations of the DAX1 (NR0B1) gene in two Taiwanese families with X-linked adrenal hypoplasia congenita. [Journal Article]
J Pediatr Endocrinol Metab 2005 Oct; 18(10):991-7.
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Lin L, Gu WX, Ozisik G, et al. 
Analysis of DAX1 (NR0B1) and steroidogenic factor-1 (SF1/Ad4BP, NR5A1) in children and adults with primary adrenal failure: ten years' experience. [JOURNAL ARTICLE]
J Clin Endocrinol Metab 2006 May 9.
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Bassett JH, O'Halloran DJ, Williams GR, et al. 
Novel DAX1 mutations in X-linked adrenal hypoplasia congenita and hypogonadotrophic hypogonadism. [Journal Article]
Clin Endocrinol (Oxf) 1999 Jan; 50(1):69-75.
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Niakan KK, McCabe ER 
DAX1 origin, function, and novel role. [Journal Article, Review]
Mol Genet Metab 2005 Sep-Oct; 86(1-2):70-83.
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