Complex Inheritance Pattern Resembling Autosomal Recessive Inheritance Involving a Microdeletion in Thrombocytopenia–Absent Radius SyndromeEva Klopocki, Stefan Mundlos, Ruth Newbury‐Ecob et al.|The American Journal of Human Genetics|2007Cited by 369
Duplications of noncoding elements 5′ of SOX9 are associated with brachydactyly-anonychiaIngo Kurth, Stefan Mundlos, Eva Klopocki et al.|Nature Genetics|2009Cited by 118
Duplications of <i>BHLHA9</i> are associated with ectrodactyly and tibia hemimelia inherited in non-Mendelian fashionEva Klopocki, Stefan Mundlos, Silke B. Lohan et al.|Journal of Medical Genetics|2011Cited by 93
ECM alterations in Fndc3a (Fibronectin Domain Containing Protein 3A) deficient zebrafish cause temporal fin development and regeneration defectsDaniel Liedtke, Eva Klopocki|Scientific Reports|2019Cited by 19