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Hay-wells syndrome of ectodermal dysplasia

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References

  1. McGrath JA, Duijf P HG, Doetsch Vet al. Hay-Wells syndrome is caused by heterozygous missense mutations in the SAM domain of p63Hum Molec Genet 2001; 10: 221–229.

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  2. Hay RJ, Wells RS. The syndrome of ankyloblepharon, ectodermal defects and cleft lip and palate: an autosomal dominant condition.Brit J Derm 1976; 94: 287–289.

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  3. Fomenkov A, Huang YP, Topaloglu Oet al. P63 alpha mutations lead to aberrant splicing of keratinocyte growth factor receptor in the Hay-Wells syndrome.J Biol Chem 2003; 278: 23906–14.

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  1. M. L. Kulkarni

    Present address: , House No. 2373, MCC'A' Block, 9th main, 577004, Davangere, Karnataka, India

Authors and Affiliations

  1. Department of Pediatrics, JJMMC, Devangere, Karnataka, India

    M. L. Kulkarni, Shilpa Deshmukh, Deepa Matani & K. Gayatri

Authors
  1. M. L. Kulkarni
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  2. Shilpa Deshmukh
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  3. Deepa Matani
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  4. K. Gayatri
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Kulkarni, M.L., Deshmukh, S., Matani, D. et al. Hay-wells syndrome of ectodermal dysplasia. Indian J Pediatr 73, 101 (2006). https://doi.org/10.1007/BF02758272

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