Watiker, Valerie; Lachman, Ralph S.; Wilcox, William R.; Barroso, In�s; Schafer, Alan J.; Scherer, Gerd (2005). „Differentiating campomelic dysplasia from Cumming syndrome”. American Journal of Medical Genetics Part A. 135A (1): 110—112. PMID15754354. S2CID27696923. doi:10.1002/ajmg.a.30650.replacement character у |first4= на позицији 3 (помоћ)
Jakobsen, L. P.; Knudsen, M. A.; Lespinasse, J.; García Ayuso, C.; Ramos, C.; Fryns, J. P.; Bugge, M.; Tommerup, N. (2006). „The genetic basis of the Pierre Robin Sequence”. The Cleft Palate-Craniofacial Journal : Official Publication of the American Cleft Palate-Craniofacial Association. 43 (2): 155—159. PMID16526920. S2CID25888887. doi:10.1597/05-008.1.
Palomo, Telma; Vilaça, Tatiane; Lazaretti-Castro, Marise (2017). „Osteogenesis imperfecta: Diagnosis and treatment”. Current Opinion in Endocrinology, Diabetes & Obesity. 24 (6): 381—388. PMID28863000. S2CID4555427. doi:10.1097/MED.0000000000000367.
Watiker, Valerie; Lachman, Ralph S.; Wilcox, William R.; Barroso, In�s; Schafer, Alan J.; Scherer, Gerd (2005). „Differentiating campomelic dysplasia from Cumming syndrome”. American Journal of Medical Genetics Part A. 135A (1): 110—112. PMID15754354. S2CID27696923. doi:10.1002/ajmg.a.30650.replacement character у |first4= на позицији 3 (помоћ)
Jakobsen, L. P.; Knudsen, M. A.; Lespinasse, J.; García Ayuso, C.; Ramos, C.; Fryns, J. P.; Bugge, M.; Tommerup, N. (2006). „The genetic basis of the Pierre Robin Sequence”. The Cleft Palate-Craniofacial Journal : Official Publication of the American Cleft Palate-Craniofacial Association. 43 (2): 155—159. PMID16526920. S2CID25888887. doi:10.1597/05-008.1.
Palomo, Telma; Vilaça, Tatiane; Lazaretti-Castro, Marise (2017). „Osteogenesis imperfecta: Diagnosis and treatment”. Current Opinion in Endocrinology, Diabetes & Obesity. 24 (6): 381—388. PMID28863000. S2CID4555427. doi:10.1097/MED.0000000000000367.
Watiker, Valerie; Lachman, Ralph S.; Wilcox, William R.; Barroso, In�s; Schafer, Alan J.; Scherer, Gerd (2005). „Differentiating campomelic dysplasia from Cumming syndrome”. American Journal of Medical Genetics Part A. 135A (1): 110—112. PMID15754354. S2CID27696923. doi:10.1002/ajmg.a.30650.replacement character у |first4= на позицији 3 (помоћ)
Jakobsen, L. P.; Knudsen, M. A.; Lespinasse, J.; García Ayuso, C.; Ramos, C.; Fryns, J. P.; Bugge, M.; Tommerup, N. (2006). „The genetic basis of the Pierre Robin Sequence”. The Cleft Palate-Craniofacial Journal : Official Publication of the American Cleft Palate-Craniofacial Association. 43 (2): 155—159. PMID16526920. S2CID25888887. doi:10.1597/05-008.1.
Palomo, Telma; Vilaça, Tatiane; Lazaretti-Castro, Marise (2017). „Osteogenesis imperfecta: Diagnosis and treatment”. Current Opinion in Endocrinology, Diabetes & Obesity. 24 (6): 381—388. PMID28863000. S2CID4555427. doi:10.1097/MED.0000000000000367.