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  • Gordon, CT (author)

Mutations in the endothelin receptor type A cause mandibulofacial dysostosis with alopecia

  • Article/chapterEnglish2015

Publisher, publication year, extent ...

  • Elsevier BV,2015

Numbers

  • LIBRIS-ID:oai:prod.swepub.kib.ki.se:131007926
  • http://kipublications.ki.se/Default.aspx?queryparsed=id:131007926URI
  • https://doi.org/10.1016/j.ajhg.2015.01.015DOI

Supplementary language notes

  • Language:English

Part of subdatabase

Classification

  • Subject category:ref swepub-contenttype
  • Subject category:art swepub-publicationtype

Added entries (persons, corporate bodies, meetings, titles ...)

  • Weaver, KN (author)
  • Zechi-Ceide, RM (author)
  • Madsen, EC (author)
  • Tavares, ALP (author)
  • Oufadem, M (author)
  • Kurihara, Y (author)
  • Adameyko, IKarolinska Institutet (author)
  • Picard, A (author)
  • Breton, S (author)
  • Pierrot, S (author)
  • Biosse-Duplan, M (author)
  • Voisin, N (author)
  • Masson, C (author)
  • Bole-Feysot, C (author)
  • Nitschke, P (author)
  • Delrue, MA (author)
  • Lacombe, D (author)
  • Guion-Almeida, ML (author)
  • Moura, PP (author)
  • Garib, DG (author)
  • Munnich, A (author)
  • Ernfors, PKarolinska Institutet (author)
  • Hufnagel, RB (author)
  • Hopkin, RJ (author)
  • Kurihara, H (author)
  • Saal, HM (author)
  • Weaver, DD (author)
  • Katsanis, N (author)
  • Lyonnet, S (author)
  • Golzio, C (author)
  • Clouthier, DE (author)
  • Amiel, J (author)
  • Karolinska Institutet (creator_code:org_t)

Related titles

  • In:American journal of human genetics: Elsevier BV96:4, s. 519-5311537-66050002-9297

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