Robinow Syndrome: Most Up-to-Date Encyclopedia, News & Reviews
Por um escritor misterioso
Descrição
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Seckel Syndrome: Most Up-to-Date Encyclopedia, News & Reviews
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Rare disorders have many faces: in silico characterization of rare
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Omodysplasia: An affected mother and son - Venditti - 2002
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Loss-of-Function GRHL3 Variants Detected in African Patients with
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Robinow syndrome: MedlinePlus Genetics
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Genes, Free Full-Text
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The Mechanism of Wnt Pathway Regulated by Telocytes to Promote the
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Children, Free Full-Text
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Common Genetic Variants Contribute to Risk of Transposition of the
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Robinow Syndrome - DoveMed
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Frontiers Diagnostic Approach to Macrocephaly in Children
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Clinical and molecular characterization of four patients with
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Dishevelled 1 - an overview
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