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)