Modelling neurofibromatosis type 1 tibial dysplasia and its treatment with lovastatin by Osswald Monika, Kossler Nadine, Kühnisch Jirko, Kolanczyk Mateusz, Stumpp Sabine, Thurisch Boris, Kornak Uwe, Mundlos Stefan

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Osteopoikilosis and multiple exostoses caused by novel mutations in <it>LEMD3 </it>and <it>EXT1 </it>genes respectively - coincidence within one family by Horn Denise, Kolanczyk Mateusz, Jamsheer Aleksander, Baasanjav Sevjidmaa, Latos Tomasz, Hoffmann Katrin, Latos-Bielenska Anna, Mundlos Stefan

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Composite transcriptome assembly of RNA-seq data in a sheep model for delayed bone healing by Mundlos Stefan, Schell Hanna, Hecht Jochen, Grünhagen Johannes, Ott Claus-Eric, Jäger Marten, Duda Georg N, Robinson Peter N, Lienau Jasmin

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Efficiency of Computer-Aided Facial Phenotyping (DeepGestalt) in Individuals With and Without a Genetic Syndrome: Diagnostic Accuracy Study by Pantel, Jean Tori, Hajjir, Nurulhuda, Danyel, Magdalena, Elsner, Jonas, Abad-Perez, Angela Teresa, Hansen, Peter, Mundlos, Stefan, Spielmann, Malte, Horn, Denise, Ott, Claus-Eric, Mensah, Martin Atta

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Gene identification and analysis of transcripts differentially regulated in fracture healing by EST sequencing in the domestic sheep by Hecht Jochen, Kuhl Heiner, Haas Stefan A, Bauer Sebastian, Poustka Albert J, Lienau Jasmin, Schell Hanna, Stiege Asita C, Seitz Volkhard, Reinhardt Richard, Duda Georg N, Mundlos Stefan, Robinson Peter N

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MIA is a potential biomarker for tumour load in neurofibromatosis type 1 by Holtkamp Nikola, Tinschert Sigrid, Thurisch Boris, Wegener Eike, Jamsheer Aleksander, Zemojtel Tomasz, Kühnisch Jirko, Nguyen Rosa, Kossler Nadine, Mautner Victor, Kolanczyk Mateusz, Park Su-Jin, Birch Patricia, Kendler David, Harder Anja, Mundlos Stefan, Kluwe Lan

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