G Koch

Congenital Secondary Hypothyroidism Caused by Exon Skipping due to a Homozygous Donor Splice Site Mutation in the TSHβ-Subunit Gene

Joachim Pohlenz, Alexandra M. Dumitrescu, Ulrich Aumann et al. · The Journal of Clinical Endocrinology & Metabolism · 2002 · 52 citations · Full text

Four New Cases of Congenital Secondary Hypothyroidism due to a Splice Site Mutation in the Thyrotropin-β Gene: Phenotypic Variability and Founder Effect

Guntram Borck, A. Kemal Topaloğlu, Eckhard Korsch et al. · The Journal of Clinical Endocrinology & Metabolism · 2004 · 31 citations

Global Alliance for the Promotion of Physical Activity: the Hamburg Declaration

Jürgen M. Steinacker, Willem van Mechelen, Wilhelm Bloch et al. · BMJ Open Sport & Exercise Medicine · 2023 · 27 citations · Full text

Physical Activity, Global Alliance, Non-communicable Disease +19

Hematopoietic Stem Cell Transplantation in an Infant with Immunodeficiency, Centromeric Instability, and Facial Anomaly Syndrome

Katharina L. Gössling, Cyrill Schipp, Ute Fischer et al. · Frontiers in Immunology · 2017 · 23 citations · Full text

Genetics of Microcephaly in Man

G Koch · Acta geneticae medicae et gemellologiae · 1959 · 18 citations

World Health Organization, Hereditary Traits, Genetics +19