1. 556 Igf1R Deletion in a Prenatal Case. (October 2012) Authors: Kammoun, M; Hichri, R; Hannechi, H; Mechmech, S; Hmida, D; Bibi, M; Saad, A; Mougou, S Journal: Archives of disease in childhood Issue: Volume 97(2012)Supplement 2 Page Start: A162 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. 738 Molecular Characterization of DER (8) (QTERQ21.13: PTERP23.3) Dn In a Child Associating Psychomotor Retardation, Hydrocephalus and Facial Dysmorphism. (October 2012) Authors: Hannachi, H; Mougou-Zerelli, S; Helal, K Ben; Abdallah, I Ben; Hmida, D; Elghezal, H; Saad, A Journal: Archives of disease in childhood Issue: Volume 97(2012)Supplement 2 Page Start: A213 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. 739 18Q22 Monosomy: Genotype-Phenotype Correlation and Therapeutic Impact. (October 2012) Authors: Kammoun, M; Hannechi, H; Hajlaoui, H; Soua, H; Hmida, D; Saad, A; Mougou, S Journal: Archives of disease in childhood Issue: Volume 97(2012)Supplement 2 Page Start: A213 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗