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Type II collagenopathies: are there additional family members?
Freisinger P, Bonaventure J, Stoess H, Pontz BF, Emmrich P, Nerlich A. Freisinger P, et al. Among authors: stoess h. Am J Med Genet. 1996 May 3;63(1):137-43. doi: 10.1002/(SICI)1096-8628(19960503)63:1<137::AID-AJMG24>3.0.CO;2-O. Am J Med Genet. 1996. PMID: 8723099
NEK1 mutations cause short-rib polydactyly syndrome type majewski.
Thiel C, Kessler K, Giessl A, Dimmler A, Shalev SA, von der Haar S, Zenker M, Zahnleiter D, Stöss H, Beinder E, Abou Jamra R, Ekici AB, Schröder-Kress N, Aigner T, Kirchner T, Reis A, Brandstätter JH, Rauch A. Thiel C, et al. Among authors: stoss h. Am J Hum Genet. 2011 Jan 7;88(1):106-14. doi: 10.1016/j.ajhg.2010.12.004. Am J Hum Genet. 2011. PMID: 21211617 Free PMC article.
[Osteoma cutis, a case report from the orthopedic viewpoint].
Wolf T, Stöss H, Ottersbach A, Breitenfelder J. Wolf T, et al. Among authors: stoss h. Z Orthop Ihre Grenzgeb. 1999 Mar-Apr;137(2):189-93. doi: 10.1055/s-2008-1039356. Z Orthop Ihre Grenzgeb. 1999. PMID: 10408065 German.
The deletion of six amino acids at the C-terminus of the alpha 1 (II) chain causes overmodification of type II and type XI collagen: further evidence for the association between small deletions in COL2A1 and Kniest dysplasia.
Winterpacht A, Superti-Furga A, Schwarze U, Stöss H, Steinmann B, Spranger J, Zabel B. Winterpacht A, et al. Among authors: stoss h. J Med Genet. 1996 Aug;33(8):649-54. doi: 10.1136/jmg.33.8.649. J Med Genet. 1996. PMID: 8863156 Free PMC article.
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