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Journal: GenesVolume: 12Number: 594
Article: Further Delineation of Phenotype and Genotype of Primary Microcephaly Syndrome with Cortical Malformations Associated with Mutations in the WDR62 Gene
- Authors:
- Ryszard Slezak1,*,
- Robert Smigiel2,* and
- Ewa Obersztyn3
- et al.
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