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Oxford University Press

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Genome Scan, Fine-Mapping, and Candidate Gene Analysis of Non-Syndromic Cleft Lip with or without Cleft Palate Reveals Phenotype-Specific Differences in Linkage and Association Results

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Identification of two AGTR2 mutations in male patients with non-syndromic mental retardation

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Identification of a New Locus for Autosomal Dominant Non-Syndromic Hearing Impairment ( DFNA7 ) in a Large Norwegian Family

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Regulatory variant in FZD6 gene contributes to nonsyndromic cleft lip and palate in an African‐American family

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