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Complex craniofacial cleft and accessory maxilla in oculoauriculofrontonasal syndrome
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Beare‐Stevenson syndrome: Two south american patients with FGFR2 analysis
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Human Fallopian Tube Mesenchymal Stromal Cells Enhance Bone Regeneration in a Xenotransplanted Model
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Craniofrontonasal Syndrome Caused by Introduction of a Novel uATG in the 5′UTR of EFNB1
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Intragenic Deletion in the LIFR Gene in a Long-Term Survivor with Stve-Wiedemann Syndrome
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Contribution of polymorphisms in genes associated with craniofacial development to the risk of nonsyndromic cleft lip and/or palate in the Brazilian population
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Reduced transcription of TCOF1 in adult cells of Treacher Collins syndrome patients
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Published in Genome research (01.07.2004)
Published in Genome research (01.07.2004)
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Published in American journal of medical genetics (01.04.1998)
Published in American journal of medical genetics (01.04.1998)
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Intragenic Deletion in the LIFR Gene in a Long-Term Survivor with Stüve-Wiedemann Syndrome
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Published in Molecular syndromology (01.07.2015)
Published in Molecular syndromology (01.07.2015)
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Beare-Stevenson syndrome: Two south american patients with FGFR2 analysis
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Published in American Journal of Medical Genetics Part A (15.08.2003)
Published in American Journal of Medical Genetics Part A (15.08.2003)
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