Point mutations throughout the GL13 gene cause Greig cephalopolysyndactyly syndrome

M Kalff-Suske, A Wild, J Topp, M Wessling, E-M Jacobsen, D Bornholdt, H (Henk) Engel, H Heuer, CM Aalfs, MGEM Ausems, R Barone, A Herzog, P Heutink, T Homfray, G Gillesson-Kaesbach, R König, J Kunze, P Meinecke, D Müller, R RizzoS Strenge, A Superti-Furga, K-H Grzeschik

Research output: Contribution to journalArticleAcademicpeer-review

106 Citations (Scopus)
Original languageUndefined/Unknown
Pages (from-to)1769-1777
Number of pages9
JournalHuman Molecular Genetics
Volume8
Issue number9
DOIs
Publication statusPublished - 1999

Research programs

  • EMC MGC-02-96-01

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