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Jump to: 2019 | 2013
Number of items: 2.

2019

Moosa, Shahida ORCID: 0000-0002-4463-3067, Yamamoto, Guilherme L., Garbes, Lutz, Keupp, Katharina, Beleza-Meireles, Ana, Moreno, Carolina Araujo, Valadares, Eugenia Ribeiro, de Sousa, Sergio B., Maia, Sofia, Saraiva, Jorge, Honjo, Rachel S., Kim, Chong Ae, de Menezes, Hamilton Cabral, Lausch, Ekkehart, Lorini, Pablo Villavicencio, Lamounier, Arsonval, Jr., Bezerra Carniero, Tulio Canella, Giunta, Cecilia ORCID: 0000-0002-9313-8257, Rohrbach, Marianne ORCID: 0000-0002-4013-6012, Janner, Marco, Semler, Oliver, Beleggia, Filippo ORCID: 0000-0003-0234-7094, Li, Yun, Yigit, Goekhan, Reintjes, Nadine, Altmueller, Janine, Nuernberg, Peter, Cavalcanti, Denise P., Zabel, Bernhard, Warman, Matthew L., Bertola, Debora R., Wollnik, Bernd and Netzer, Christian (2019). Autosomal-Recessive Mutations in MESD Cause Osteogenesis Imperfecta. Am. J. Hum. Genet., 105 (4). S. 836 - 844. CAMBRIDGE: CELL PRESS. ISSN 1537-6605

2013

Grosch, Melanie, Gruener, Barbara, Spranger, Stephanie, Stuetz, Adrian M., Rausch, Tobias ORCID: 0000-0001-5773-5620, Korbel, Jan O., Seelow, Dominik ORCID: 0000-0002-9746-4412, Nuernberg, Peter, Sticht, Heinrich ORCID: 0000-0001-5644-045X, Lausch, Ekkehart, Zabel, Bernhard, Winterpacht, Andreas and Tagariello, Andreas (2013). Identification of a Ninein (NIN) mutation in a family with spondyloepimetaphyseal dysplasia with joint laxity (leptodactylic type)-like phenotype. Matrix Biol., 32 (7-8). S. 387 - 393. AMSTERDAM: ELSEVIER SCIENCE BV. ISSN 1569-1802

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