<style face="normal" font="default" size="100%">De novo 911 Kb interstitial deletion on chromosome 1q43 in a boy with mental retardation and short stature.</style>

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<style face="normal" font="default" size="100%">De novo 911 Kb interstitial deletion on chromosome 1q43 in a boy with mental retardation and short stature.</style>

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<style face="normal" font="default" size="100%">Identification of a New Mutation (L46P) in the Human NOG Gene in an Italian Patient with Symphalangism Syndrome.</style>

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<style face="normal" font="default" size="100%">Phylloid pattern of hypomelanosis closely related to chromosomal abnormalities in the 13q detected by SNP array analysis.</style>

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<style face="normal" font="default" size="100%">Two Novel COH1 Mutations in an Italian Patient with Cohen Syndrome.</style>