Branchio-oto-renal syndrome: detection of EYA1 and SIX1 mutations in five out of six Danish families by combining linkage, MLPA and sequencing analyses

Research output: Contribution to journalJournal articleResearchpeer-review

Udgivelsesdato: 2007/11
Original languageEnglish
JournalEuropean Journal of Human Genetics
Volume15
Issue number11
Pages (from-to)1121-1131
Number of pages10
ISSN1018-4813
Publication statusPublished - 2007

ID: 4041772