Neonatal Features of the Prader-Willi Syndrome; The Case for Making the Diagnosis During the First Week of Life

Bằng Çizmecioğlu, Filiz Mine, Jones, Jeremy Huw, Paterson, Wendy Forsyth, Kherra, Sakina, Kourime, Mariam, McGowan, Ruth, Shaikh, M. Guftar, Donaldson, Malcolm
Xuất bản năm J Clin Res Pediatr Endocrinol (2018)

Familial Multiplicity of Estrogen Insensitivity Associated With a Loss-of-Function ESR1 Mutation

Bằng Bernard, Valérie, Kherra, Sakina, Francou, Bruno, Fagart, Jérôme, Viengchareun, Say, Guéchot, Jérôme, Ladjouze, Asmahane, Guiochon-Mantel, Anne, Korach, Kenneth S., Binart, Nadine, Lombès, Marc, Christin-Maitre, Sophie
Xuất bản năm J Clin Endocrinol Metab (2016)