ey0015.6-19 | Reviews of clinical importance | ESPEYB15
6.19 Disorders of sex development
ey0015.6-15 | When should an extensive genetic investigation be performed? | ESPEYB15
6.15 Mutations involving the SRY-related gene SOX8 are associated with a spectrum of human reproductive anomalies
MF Portnoi , MC Dumargne , S Rojo , SF Witchel , AJ Duncan , C Eozenou , J Bignon-Topalovic , SA Yatsenko , A Rajkovic , M Reyes-Mugica , K Almstrup , L Fusee , Y Srivastava , S Chantot-Bastaraud , C Hyon , C Louis-Sylvestre , P Validire , C de Malleray Pichard , C Ravel , S Christin-Maitre , R Brauner , R Rossetti , L Persani , EH Charreau , L Dain , VA Chiauzzi , I Mazen , H Rouba , C Schluth-Bolard , S MacGowan , WHI McLean , E Patin , E Rajpert-De Meyts , R Jauch , JC Achermann , JP Siffroi , K McElreavey , A Bashamboo
ESPE Yearbook of Paediatric Endocrinology
ISSN 1662-4009 (Online)
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