论文信息 - Novel genetic variants of KHDC3L and other members of the subcortical maternal complex associated with Beckwith–Wiedemann syndrome or Pseudohypoparathyroidism 1B and multi-locus imprinting disturbances - 字舞流文

Novel genetic variants of KHDC3L and other members of the subcortical maternal complex associated with Beckwith–Wiedemann syndrome or Pseudohypoparathyroidism 1B and multi-locus imprinting disturbances

M. Esteller | P. Lapunzina | A. Verma | M. Carella | M. Cubellis | D. Monk | P. Prontera | M. Accadia | B. Hay Mele | O. Palumbo | A. Riccio | Laura Pignata | A. Sparago | M. Monticelli | F. Cerrato | C. Piscopo | Basilia Acurzio | Guiomar Pérez de Nanclares | Arrate Pereda | Ana Monteagudo-Sánchez | Francesco Cecere | J. Tenorio-Castaño | Carlo Giaccari | J. R. Hernández Mora | A. Pereda | G. D. de Nanclares