Mutations in endothelin 1 cause recessive auriculocondylar syndrome and dominant isolated question-mark ears
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author: Stanislas Lyonnet, Patrick Nitschké, Christine Bôle-Feysot, Roseli Maria Zechi-Ceide, Frédéric Tores, Nancy Mizue Kokitsu-Nakata, Christopher T. Gordon, Florence Petit, Jeanne Amiel, Arnold Munnich, Maria Leine Guion-Almeida, Siulan Vendramini-Pittoli, Peter Kroisel, Cécile Masson, Myriam Oufadem, Linda Jakobsen, Solenn Pruvost, Pernille Lindholm, Philippe Pellerin, Muriel Holder-Espinasse
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