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Publications by Louise C. Wilson

Natural History and Genotype-Phenotype Correlations in 72 Individuals With SATB2 -Associated Syndrome

American Journal of Medical Genetics, Part A

English

The Origin of EFNB1 Mutations in Craniofrontonasal Syndrome: Frequent Somatic Mosaicism and Explanation of the Paucity of Carrier Males

American Journal of Human Genetics

English