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1
Mutations in endothelin 1 cause recessive auriculocondylar syndrome and dominant isolated question-mark ears
Mutations in endothelin 1 cause recessive auriculocondylar syndrome and dominant isolated question-mark ears
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Mutations in endothelin 1 cause recessive auriculocondylar syndrome and dominant isolated question-mark ears

Christopher J Gordon Florence Petit; Peter Michael Kroisel; Linda Jakobsen; Roseli Maria Zechi-Ceide; Myriam Oufadem; C Bole-Feysot; Solenn Pruvost; Cécile Masson; Frédéric Tores; Thierry Hieu; Patrick Nitschké; Pernille Lindholm; Philippe Pellerin; Maria Leine Guion-Almeida; Nancy Mizue Kokitsu Nakata; Siulan Vendramini Paulovich Pittoli; Arnold Munnich; Stanislas Lyonnet; Muriel Holder-Espinasse; Jeanne Amiel

American Journal of Human Genetics Chicago v. 93, n. 6, p. 1118-1125, Dec. 2013

Chicago 2013

Item não circula. Consulte sua biblioteca.(Acessar)

2
Mutations in the endothelin receptor type A cause mandibulofacial dysostosis with alopecia
Mutations in the endothelin receptor type A cause mandibulofacial dysostosis with alopecia
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Mutations in the endothelin receptor type A cause mandibulofacial dysostosis with alopecia

Christopher T Gordon K. Nicole Weaver; Roseli Maria Zechi-Ceide; Erik C Madsen; Andre L. P Tavares; Myriam Oufadem; Yukiko Kurihara; Igor Adameyko; Arnaud Picard; Sylvain Breton; Sébastien Pierrot; Martin Biosse-Duplan; Norine Voisin; Cécile Masson; Christine Bole-Feysot; Patrick Nitschké; Marie-Ange Delrue; Didier Lacombe; Maria Leine Guion-Almeida; Priscila Padilha Moura; Daniela Gamba Garib; Arnold Munnich; Patrik Ernfors; Robert B Hufnagel; Robert J Hopkin

American Journal of Human Genetics Chicago v. 96, n. 4, p. 519-531, Apr. 2015

Chicago 2015

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Deste Autor:

  1. Gordon, C
  2. Oufadem, M
  3. Zechi-Ceide, R
  4. Guion-Almeida, M
  5. Bole-Feysot, C

Neste Assunto:

  1. Disostose Mandibulofacial
  2. Alopecia
  3. Fenótipos
  4. Otopatias
  5. Endotelinas

  • Realização: ABCD-USP USP   Logos de Redes Sociais: Freepik

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