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pro vyhledávání: '"M. G�tz-Sothmann"'
Autor:
P. Steinbach, D. W�hrle, G. Tariverdian, I. Kennerknecht, G. Barbi, H. Edlinger, H. Enders, M. G�tz-Sothmann, H. Heilbronner, D. Hosenfeld, R. Kircheisen, F. Majewski, P. Meinecke, E. Passarge, A. Schmidt, H. Seidel, G. Wolff, M. Zank
Publikováno v:
Human Genetics. 92:491-498
Molecular genetic analysis of the transmission of mutations in 73 families with fragile X (one of the largest samples evaluated so far) has confirmed previous hypotheses that the fragile X syndrome results from two consecutive mutational steps, desig
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4250e41e4f8ca758bfa1603778aee4cb
https://doi.org/10.1007/bf00216457
https://doi.org/10.1007/bf00216457
