Genetic causes of microcephaly and lessons for neuronal development
Author:
Publisher
Wiley
Subject
Cell Biology,Developmental Biology,Molecular Biology
Reference179 articles.
1. The predictive value of microcephaly during the first year of life for mental retardation at seven years;Dolk;Dev Med Child Neurol,1991
2. Whole-exome sequencing identifies recessive WDR62 mutations in severe brain malformations;Bilguvar;Nature,2010
3. Mutations in WDR62, encoding a centrosome-associated protein, cause microcephaly with simplified gyri and abnormal cortical architecture;Yu;Nat Genet,2010
4. WDR62 is associated with the spindle pole and is mutated in human microcephaly;Nicholas;Nat Genet,2010
5. Retrospective birth dating of cells in humans;Spalding;Cell,2005
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