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Journal Article
Garbes, Lutz, Kim, Kyungho, Riess, Angelika, Hoyer-Kuhn, Heike, Beleggia, Filippo ORCID: 0000-0003-0234-7094, Bevot, Andrea, Kim, Mi Jeong, Huh, Yang Hoon, Kweon, Hee-Seok, Savarirayan, Ravi, Amor, David, Kakadia, Purvi M., Lindig, Tobias, Kagan, Karl Oliver, Becker, Jutta, Boyadjiev, Simeon A., Wollnik, Bernd, Semler, Oliver
ORCID: 0000-0003-0029-7556, Bohlander, Stefan K., Kim, Jinoh
ORCID: 0000-0003-2841-147X and Netzer, Christian
(2015).
Mutations in SEC24D, Encoding a Component of the COPII Machinery, Cause a Syndromic Form of Osteogenesis Imperfecta.
Am. J. Hum. Genet., 96 (3).
S. 432 - 440.
CAMBRIDGE:
CELL PRESS.
ISSN 1537-6605
Garbes, Lutz, Kim, Kyungho, Riess, Angelika, Hoyer-Kuhn, Heike, Beleggia, Filippo ORCID: 0000-0003-0234-7094, Bevot, Andrea, Kim, Mi Jeong, Huh, Yang Hoon, Kweon, Hee-Seok, Savarirayan, Ravi, Amor, David, Kakadia, Purvi M., Lindig, Tobias, Kagan, Karl Oliver, Becker, Jutta, Boyadjiev, Simeon A., Wollnik, Bernd, Semler, Oliver
ORCID: 0000-0003-0029-7556, Bohlander, Stefan K., Kim, Jinoh
ORCID: 0000-0003-2841-147X and Netzer, Christian
(2015).
Mutations in SEC24D, Encoding a Component of the COPII Machinery, Cause a Syndromic Form of Osteogenesis Imperfecta.
Am. J. Hum. Genet., 96 (3).
S. 432 - 440.
CAMBRIDGE:
CELL PRESS.
ISSN 1537-6605
Kagan, Karl Oliver, Berg, Christoph, Dufke, Andreas, Geipel, Annegret, Hoopmann, Markus and Abele, Harald (2015). Novel fetal and maternal sonographic findings in confirmed cases of Beckwith-Wiedemann syndrome. Prenat. Diagn., 35 (4). S. 394 - 400. HOBOKEN: WILEY-BLACKWELL. ISSN 1097-0223
Kagan, Karl Oliver, Berg, Christoph, Dufke, Andreas, Geipel, Annegret, Hoopmann, Markus and Abele, Harald (2015). Novel fetal and maternal sonographic findings in confirmed cases of Beckwith-Wiedemann syndrome. Prenat. Diagn., 35 (4). S. 394 - 400. HOBOKEN: WILEY-BLACKWELL. ISSN 1097-0223