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Autor:
Anju K Philips, Pinelli M, Ci, Bie, Mustonen A, Määttä T, Hh, Arts, Wu K, Roepman R, Js, Moilanen, Raza S, Varilo T, Scala G, Cocozza S, Gilissen C, Kl, Gassen, Järvelä I
Publikováno v:
Clinical Genetics, 91, 1, pp. 100-105
Europe PubMed Central
Clinical Genetics, 91, 100-105
Clinical Genetics, 91(1), 100. Wiley-Blackwell
Europe PubMed Central
Clinical Genetics, 91, 100-105
Clinical Genetics, 91(1), 100. Wiley-Blackwell
Contains fulltext : 169700.pdf (Publisher’s version ) (Closed access) Intellectual disability (ID) is a major health problem in our society. Genetic causes of ID remain unknown because of its vast heterogeneity. Here we report two Finnish families
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::018b7c0ed747049cc658a558594d7f84
https://hdl.handle.net/2066/169700
https://hdl.handle.net/2066/169700