FGF17, a gene involved in cerebellar development, is downregulated in a patient with Dandy-Walker malformation carrying a de novo 8p deletion

Neurogenetics

Volumn 12, Issue 3, 2011, Pages 241-245

  Zanni, Ginevra ^a   Barresi, Sabina ^a   Travaglini, Lorena ^a   Bernardini, Laura ^b   Rizza, Teresa ^a   Digilio, Maria Cristina ^a   Mercuri, Eugenio ^c   Cianfarani, Stefano ^a   Valeriani, Massimiliano ^a   Ferraris, Alessandro ^b   Da Sacco, Letizia ^a   Novelli, Antonio ^b   Valente, Enza Maria ^b   Dallapiccola, Bruno ^a   Bertini, Enrico Silvio ^a  

^a BAMBINO GESÙ CHILDREN S HOSPITAL   (Italy)

^b CASA SOLLIEVO DELLA SOFFERENZA HOSPITAL   (Italy)

^c CATHOLIC UNIVERSITY   (Italy)

Author keywords

Cerebellum; Chromosome 8p; Dandy Walker malformation; FGF17

Indexed keywords

FIBROBLAST GROWTH FACTOR;

ARTICLE; BRAIN DEVELOPMENT; CASE REPORT; CHILD; CHROMOSOME 8P; CHROMOSOME DELETION; DANDY WALKER SYNDROME; FEMALE; FGF17 GENE; GENE; GENE DISRUPTION; GENE EXPRESSION; GROWTH RETARDATION; HUMAN; PRIORITY JOURNAL; SEIZURE; TRANSCRIPTION REGULATION;

CEREBELLUM; CHILD, PRESCHOOL; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 8; COMPARATIVE GENOMIC HYBRIDIZATION; DANDY-WALKER SYNDROME; DOWN-REGULATION; FEMALE; FIBROBLAST GROWTH FACTOR 8; GENE EXPRESSION PROFILING; HUMANS;

MUS; VERTEBRATA;

EID: 80052766863     PISSN: 13646745     EISSN: 13646753     Source Type: Journal    
DOI: 10.1007/s10048-011-0283-8     Document Type: Article

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