(Q45975520)
Statements
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Predominant Sertoli cell deficiency in a 46,XY disorders of sex development patient with a new NR5A1/SF-1 mutation transmitted by his unaffected father. (English)
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Stephen Lortat-Jacob
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Michel Polak
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Ana Colmenares
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Françoise Audran
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Francis Poulat
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Charles Sultan
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15 December 2010
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95
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5
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1788.e5-9
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