Normal intelligence and premature ovarian failure in an adult female with a 7.6 Mb de novo terminal deletion of chromosome 9p

Combined Immunodeficiency Associated with <i>DOCK8</i> Mutations

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Clinical and cytogenetic characterization of 13 Dutch patients with deletion 9p syndrome: Delineation of the critical region for a consensus phenotype

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Deletion of the short arm of chromosome no.9 (46,9p-): a new deletion syndrome.

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DMRT1 promotes oogenesis by transcriptional activation of Stra8 in the mammalian fetal ovary

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