المؤلفون: Sanja Brajnović-Zaputović, Bojana Brajenović-Milić, Silvija Kamber-Makek, Ela Paučić-Kirinčić, Antun Sasso, Nada Sindičić

المصدر: Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery. 24(5)

مصطلحات موضوعية: Male, Mowat–Wilson syndrome, medicine.disease_cause, Exon, Congenital syndrome, Hirschsprung disease, Seizures, Mental retardation, ZFHX1B gene, Clinical report, Intellectual Disability, medicine, Humans, Abnormalities, Multiple, Child, Gene, Zinc Finger E-box Binding Homeobox 2, Genetics, Chromosome Aberrations, Homeodomain Proteins, Mutation, business.industry, Chromosome, General Medicine, Exons, medicine.disease, Repressor Proteins, Pediatrics, Perinatology and Child Health, Neurology (clinical), business, Novel mutation

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::722bf102e9df5546f5f648242baf3597
https://pubmed.ncbi.nlm.nih.gov/18259761

المؤلفون: Antun Sasso, Ela Paučić-Kirinčić, Silvija Kamber-Makek, Nada Sindičić, S. Brajnović-Zaputović, Bojana Brajenović-Milić

المصدر: Child's Nervous System; May2008, Vol. 24 Issue 5, p615-618, 4p

مصطلحات موضوعية: GENETIC mutation, HUMAN abnormalities, INTELLECTUAL disabilities, GENETIC polymorphisms