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Miscarriages in Families with a Child with Classic Congenital Adrenal Hyperplasia and 21-Hydroxylase Deficiency (CAH) | ESPE2018
Theresa Penger; Johannes Hess; Michaela Marx; Patricia Oppelt; Helmuth-Gunther Dorr
http://abstracts.eurospe.org/hrp/0089/hrp0089p2-p007.htm
Published: 2018-08-28

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Time Trends in Baseline Characteristics (2006-2014) in Short Children with Growth Hormone Deficiency (GHD), Born Small for Gestational Age (SGA) and with Ullrich-Turner Syndrome (TS) Enrolled in Nordinet[reg] International Outcomes Study (IOS) in Germany and Czech Republic | ESPE2015
Helmuth Gunther Dorr; Jurgen Bramswig; Stefanie Meckes-Ferber; Effie Pournara; Birgitte Tonnes Pedersen; Marta Snajderova
http://abstracts.eurospe.org/hrp/0084/hrp0084p3-972.htm
Published: 2015-08-26

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Allelic Frequencies of CYP21A2 Variants and Genotype-Phenotype Correlations in a Cohort of 660 CAH Patients from Germany and Austria | ESPE2014
Stefan Riedl; Friedrich-Wilhelm Rohl; Susann Empting; Walter Bonfig; Helmuth-Gunther Dorr; Reinhard Holl; Klaus Mohnike
http://abstracts.eurospe.org/hrp/0082/hrp0082p1-d2-1.htm
Published: 2014-08-28

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