Search Results - "Berten, H.‐L."

Identification of novel CBFA1/RUNX2 mutations causing cleidocranial dysplasia by Bergwitz, C., Prochnau, A., Mayr, B., Kramer, F.‐J., Rittierodt, M., Berten, H.‐L., Hausamen, J.‐E., Brabant, G.

“…Core binding factor A1 (CBFA1/RUNX2) is a runt‐like transcription factor essential for osteoblast differentiation. Haplotype insufficiency causes cleidocranial…”
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Injuries of the midface in childhood by Neukam, F W, Schliephake, H, Berten, H L, Hausamen, J E

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