The origin of EFNB1 mutations in craniofrontonasal syndrome: frequent somatic mosaicism and explanation of the paucity of carrier males (Q24546616)
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(P1476) "The origin of EFNB1 mutations in craniofrontonasal syndrome: frequent somatic mosaicism and explanation of the paucity of carrier males" (language: en)
(P2093) Stephen R F Twigg
Kazuya Matsumoto
Alexa M J Kidd
Indira B Taylor
Richard B Fisher
A Jeannette M Hoogeboom
Irene M J Mathijssen
M Teresa Lourenco
Jenny E V Morton
Elizabeth Sweeney
Louise C Wilson
John B Mulliken
Steven A Wall
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