A. Receveur
AuthID: R-00G-PZA
1
TÃTULO: A novel microdeletion syndrome at 3q13.31 characterised by developmental delay, postnatal overgrowth, hypoplastic male genitals, and characteristic facial features
AUTORES: Molin, AM; Andrieux, J; Koolen, DA; Malan, V; Carella, M; Colleaux, L; Cormier Daire, V; David, A; de Leeuw, N; Delobel, B; Duban Bedu, B; Fischetto, R; Flinter, F; Kjaergaard, S; Kok, F; Krepischi, AC; Le Caignec, C; Mackie M Ogilvie; Maia, S; Mathieu Dramard, M; ...Mais
PUBLICAÇÃO: 2012, FONTE: JOURNAL OF MEDICAL GENETICS, VOLUME: 49, NÚMERO: 2
AUTORES: Molin, AM; Andrieux, J; Koolen, DA; Malan, V; Carella, M; Colleaux, L; Cormier Daire, V; David, A; de Leeuw, N; Delobel, B; Duban Bedu, B; Fischetto, R; Flinter, F; Kjaergaard, S; Kok, F; Krepischi, AC; Le Caignec, C; Mackie M Ogilvie; Maia, S; Mathieu Dramard, M; ...Mais
PUBLICAÇÃO: 2012, FONTE: JOURNAL OF MEDICAL GENETICS, VOLUME: 49, NÚMERO: 2
