J. Kern

发表

Hereditary and environmental dental findings in identification of human remains.

S. Blažeković-Milaković, J. Kern, M. Kulenović, 2000 .

A familial case of tricho‐rhino‐phalangeal syndrome type III with a novel missense mutation in exon 6 of the TRPS1 gene

D. Nashan, L. Bruckner-Tuderman, H. Lüdecke, 2010, Journal of the European Academy of Dermatology and Venereology : JEADV.

Chronic colitis due to an epithelial barrier defect: the role of kindlin‐1 isoforms

E. Haan, C. Herz, O. Opitz, 2007, The Journal of pathology.