R. Mühlenberg

Silver-Russell patients showing a broad range of ICR1 and ICR2 hypomethylation in different tissues

Matthias Begemann, Sabrina Spengler, Deniz Kanber et al. · Clinical Genetics · 2010 · 64 citations

Growth Retardation in Turner Syndrome: Aneuploidy, Rather Than Specific Gene Loss, May Explain Growth Failure

F. Haverkamp, Joachim Wölfle, Klaus Zerres et al. · The Journal of Clinical Endocrinology & Metabolism · 1999 · 37 citations · Full text

Short Stature, Human Growth, Cytogenetics +19

A New C-Terminal Located Mutation (V272ter) in the <i>PIT-1 </i>Gene Manifesting with Severe Congenital Hypothyroidism

Oliver Blankenstein, R. Mühlenberg, C. Kim et al. · Hormone Research in Paediatrics · 2001 · 29 citations

Mild Congenital Primary Hypothyroidism in a Turkish Family Caused by a Homozygous Missense Thyrotropin Receptor (TSHR) Gene Mutation (A593 V)

Susanne Fricke‐Otto, Nicole Pfarr, R. Mühlenberg et al. · Experimental and Clinical Endocrinology & Diabetes · 2005 · 22 citations

Developmental Biology, Genetic Disorder, Genetics +12

Congenital Goitrous Primary Hypothyroidism in Two German Families Caused by Novel Thyroid Peroxidase (TPO) Gene Mutations

Karina Altmann, Pia Hermanns, R. Mühlenberg et al. · Experimental and Clinical Endocrinology & Diabetes · 2013 · 10 citations

Novel Thyroid Peroxidase, Developmental Biology, Thyroid Hormone Synthesis +13