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The Journal of Clinical Endocrinology and Metabolism|April 22, 2011
Gonadal pathology and tumor risk in relation to clinical characteristics in patients with 45,X/46,XY mosaicismM Cools, J Pleskacova, H Stoop, et al.
Diabetic Medicine : a Journal of the British Diabetic Association|August 20, 2013
The dynamic changes of zinc transporter 8 autoantibodies in Czech children from the onset of Type 1 diabetes mellitusL Petruzelkova, R Ananieva-Jordanova, J Vcelakova, et al.
Sexual Development : Genetics, Molecular Biology, Evolution, Endocrinology, Embryology, and Pathology of Sex Determination and Differentiation|November 20, 2013
45,X/46,X,psu dic(Y) gonadal dysgenesis: influence of the two cell lines on the clinical phenotype, including gonadal histologyJ Kaprova-Pleskacova, M Snajderova, J Stoop, et al.
European Journal of Endocrinology|July 5, 2005
Mutational spectrum of steroid 21-hydroxylase and the genotype-phenotype association in Middle European patients with congenital adrenal hyperplasiaV Dolzan, J Sólyom, G Fekete, et al.
Diabetologia|April 15, 2005
Molecular genetics and phenotypic characteristics of MODY caused by hepatocyte nuclear factor 4alpha mutations in a large European collectionE R Pearson, S Pruhova, C J Tack, et al.
Diabetologia|August 9, 2011
Homozygous carriers of the G allele of rs4664447 of the glucagon gene (GCG) are characterised by decreased fasting and stimulated levels of insulin, glucagon and glucagon-like peptide (GLP)-1S S Torekov, L Ma, N Grarup, et al.
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