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

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Description scientific article
Author/s

author: Cécile Masson  Myriam Oufadem  Pernille Lindholm  Muriel Holder-Espinasse  Linda Jakobsen  Solenn Pruvost  Patrick Nitschké  Frédéric Tores  Christine Bôle-Feysot  Christopher T Gordon  Jeanne Amiel  Roseli Maria Zechi-Ceide  Maria Leine Guion-Almeida  Stanislas Lyonnet  Arnold Munnich  Peter Kroisel  Philippe Pellerin  Siulan Vendramini-Pittoli  Nancy Mizue Kokitsu-Nakata  Florence Petit 

Publication date November 21, 2013
Language English
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