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pro vyhledávání: '"Silvija Kamber-Makek"'
Autor:
Sanja Brajnović-Zaputović, Bojana Brajenović-Milić, Silvija Kamber-Makek, Ela Paučić-Kirinčić, Antun Sasso, Nada Sindičić
Publikováno v:
Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery. 24(5)
Mowat-Wilson syndrome is a congenital syndrome caused by a defect of the transcriptional repressor ZFHX1B (SIP1) gene on the chromosome 2q22-q23. The genotype-phenotype analysis confirmed that ZFHX1B deletions and mutations result in a recognizable f
Autor:
Antun Sasso, Ela Paučić-Kirinčić, Silvija Kamber-Makek, Nada Sindičić, S. Brajnović-Zaputović, Bojana Brajenović-Milić
Publikováno v:
Child's Nervous System; May2008, Vol. 24 Issue 5, p615-618, 4p