Hyper- und Hypoparathyreoidismus
Author:
Publisher
Springer Berlin Heidelberg
Link
http://link.springer.com/content/pdf/10.1007/978-3-642-56858-9_4.pdf
Reference139 articles.
1. Aaltonen J, Bjorses P, Sandkuijl L, Perheentupa J, Peltonen L (1994) An autosomal locus causing autoimmune disease, autoimmune polyglandular disease typ I assigned to chromosome 21. Nat Genet 8:83–87
2. Abdel AY, Auger LT, El-Gharbawy F (1989) Kenny-Caffey syndrome. Case report and literature review. Clin Pediatr (Phila) 28:175–179
3. Abramowicz MJ, Cochaux P, Cohen LH, Vamos E (1996) Pernicious anaemia and hypoparathyroidism in a patient with Kearns-Sayre syndrome with mitochondrial DNA duplication. J Inherit Metab Dis 19:109–111
4. Agarwal SK, Kester MB, Debelenko LV et al. (1997) Germline mutat ions of the MEN 1 gene in familial multiple endocrine neoplasia type land related states. Hum Mol Genet 6:1169–1175
5. Ahonen P (1985) Autoimmune polyendocrinopathy-candidosis-ectodermal dystrophy (APECED): autosomal recessive inheritance. Clin Genet 27:535–542
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