Hasi-Zogaj M, Sebold C, Heard P, Carter E, Soileau B, Hill A, Rupert D, Perry B, Atkinson S, O'Donnell L, Gelfond J, Lancaster J, Fox PT, Hale DE, Cody JD (2015). "A review of 18p deletions". Am J Med Genet C Semin Med Genet. 169 (3): 251–64. doi:10.1002/ajmg.c.31445. PMID26250845. S2CID20556694.
Faust, J.; habedank, M.; Nieuwenhuijsen, C. (1976). "The 18 p- syndrome". European Journal of Pediatrics. 123 (1). Springer Science and Business Media LLC: 59–66. doi:10.1007/bf00497681. ISSN0340-6997. PMID954771.
Wester, Ulrika; Bondeson, Marie-Louise; Edeby, Christina; Annerén, Göran (2006-05-11). "Clinical and molecular characterization of individuals with 18p deletion: A genotype–phenotype correlation". American Journal of Medical Genetics Part A. 140A (11). Wiley: 1164–1171. doi:10.1002/ajmg.a.31260. ISSN1552-4825. PMID16691587.
Grosso, S.; Pucci, L.; Di Bartolo, R.M.; Gobbi, G.; Bartalini, G.; Anichini, C.; Scarinci, R.; Balestri, M.; Farnetani, M.A.; Cioni, M.; Morgese, G.; Balestri, P. (2005). "Chromosome 18 aberrations and epilepsy: A review". American Journal of Medical Genetics Part A. 134A (1). Wiley: 88–94. doi:10.1002/ajmg.a.30575. ISSN1552-4825. PMID15690352.
Cohen, M. Michael (2006). "Holoprosencephaly: Clinical, anatomic, and molecular dimensions". Birth Defects Research Part A: Clinical and Molecular Teratology. 76 (9). Wiley: 658–673. doi:10.1002/bdra.20295. ISSN1542-0752. PMID17001700.
Münke, Maximilian; Page, David C.; Brown, Laura G.; Armson, B. Anthony; Zackai, Elaine H.; Mennuti, Michael T.; Emanuel, Beverly S. (1988). "Molecular detection of a Yp/18 translocation in a 45,X holoprosencephalic male". Human Genetics. 80 (3). Springer Science and Business Media LLC: 219–223. doi:10.1007/bf01790089. ISSN0340-6717. PMID3192211.
Dharmaraj, P; Grueters, A (2006). "The management of thyrotoxicosis in a pre-pubertal child with 18p deletion syndrome". European Journal of Endocrinology. 155 (suppl_1): S145 –S147. doi:10.1530/eje.1.02274. ISSN0804-4643.
Kantaputra, Piranit N.; Limwongse, Chanin; Tochareontanaphol, Chintana; Mutirangura, Apiwat; Mevatee, Umnat; Praphanphoj, Verayuth (2006-09-25). "Contiguous gene syndrome of holoprosencephaly and hypotrichosis simplex: Association with an 18p11.3 deletion". American Journal of Medical Genetics Part A. 140A (23). Wiley: 2598–2602. doi:10.1002/ajmg.a.31386. ISSN1552-4825. PMID17001671.
Nazarenko, S. A.; Ostroverkhova, N. V.; Vasiljeva, E. O.; Nazarenko, L. P.; Puzyrev, V. P.; Malet, P.; Nemtseva, T. A. (1999-07-16). "Keratosis pilaris and ulerythema ophryogenes associated with an 18p deletion caused by a Y/18 translocation". American Journal of Medical Genetics. 85 (2): 179–182. doi:10.1002/(SICI)1096-8628(19990716)85:2<179::AID-AJMG14>3.0.CO;2-R. ISSN0148-7299. PMID10406673.
Klein, C.; Page, C.E.; LeWitt, P.; Gordon, M.F.; de Leon, D.; Awaad, Y.; Breakefield, X.O.; Brin, M.F.; Ozelius, L.J. (1999). "Genetic analysis of three patients with an 18p− syndrome and dystonia". Neurology. 52 (3). Ovid Technologies (Wolters Kluwer Health): 649–651. doi:10.1212/wnl.52.3.649. ISSN0028-3878. PMID10025808.
Nasir, Jamal; Frima, Nafsika; Pickard, Ben; Malloy, M. Pat; Zhan, Lingping; Grünewald, Richard (2006-06-06). "Unbalanced whole arm translocation resulting in loss of 18p in dystonia". Movement Disorders. 21 (6). Wiley: 859–863. doi:10.1002/mds.20846. ISSN0885-3185. PMID16541453.
Wang, Jin-Chen C.; Nemana, L.; Kou, S. Y.; Habibian, R.; Hajianpour, M. J. (1997-09-05). "Molecular cytogenetic characterization of 18;21 whole arm translocation associated with monosomy 18p". American Journal of Medical Genetics. 71 (4): 463–466. doi:10.1002/(SICI)1096-8628(19970905)71:4<463::AID-AJMG17>3.0.CO;2-E. PMID9286456.
Babovic-Vuksanovic, Dusica; Jenkins, S.C.; Ensenauer, R.; Newman, D.C.; Jalal, S.M. (2003-06-30). "Subtelomeric deletion of 18p in an adult with paranoid schizophrenia and mental retardation". American Journal of Medical Genetics Part A. 124A (3). Wiley: 318–322. doi:10.1002/ajmg.a.20391. ISSN1552-4825. PMID14708108.
Rigola, M.A.; Plaja, A.; Mediano, C.; Miro, R.; Egozcue, J.; Fuster, C. (2001). "Characterization of a heritable partial monosomy 18p by molecular and cytogenetic analysis". American Journal of Medical Genetics. 104 (1). Wiley: 37–41. doi:10.1002/ajmg.1584. ISSN0148-7299. PMID11746025.
de Ravel, Thomy J.L.; Thiry, Paul; Fryns, Jean-Pierre (2005). "Follow-up of adult males with chromosome 18p deletion". European Journal of Medical Genetics. 48 (2). Elsevier BV: 189–193. doi:10.1016/j.ejmg.2005.01.024. ISSN1769-7212. PMID16053911.
Hasi-Zogaj M, Sebold C, Heard P, Carter E, Soileau B, Hill A, Rupert D, Perry B, Atkinson S, O'Donnell L, Gelfond J, Lancaster J, Fox PT, Hale DE, Cody JD (2015). "A review of 18p deletions". Am J Med Genet C Semin Med Genet. 169 (3): 251–64. doi:10.1002/ajmg.c.31445. PMID26250845. S2CID20556694.
Faust, J.; habedank, M.; Nieuwenhuijsen, C. (1976). "The 18 p- syndrome". European Journal of Pediatrics. 123 (1). Springer Science and Business Media LLC: 59–66. doi:10.1007/bf00497681. ISSN0340-6997. PMID954771.
Wester, Ulrika; Bondeson, Marie-Louise; Edeby, Christina; Annerén, Göran (2006-05-11). "Clinical and molecular characterization of individuals with 18p deletion: A genotype–phenotype correlation". American Journal of Medical Genetics Part A. 140A (11). Wiley: 1164–1171. doi:10.1002/ajmg.a.31260. ISSN1552-4825. PMID16691587.
Grosso, S.; Pucci, L.; Di Bartolo, R.M.; Gobbi, G.; Bartalini, G.; Anichini, C.; Scarinci, R.; Balestri, M.; Farnetani, M.A.; Cioni, M.; Morgese, G.; Balestri, P. (2005). "Chromosome 18 aberrations and epilepsy: A review". American Journal of Medical Genetics Part A. 134A (1). Wiley: 88–94. doi:10.1002/ajmg.a.30575. ISSN1552-4825. PMID15690352.
Cohen, M. Michael (2006). "Holoprosencephaly: Clinical, anatomic, and molecular dimensions". Birth Defects Research Part A: Clinical and Molecular Teratology. 76 (9). Wiley: 658–673. doi:10.1002/bdra.20295. ISSN1542-0752. PMID17001700.
Münke, Maximilian; Page, David C.; Brown, Laura G.; Armson, B. Anthony; Zackai, Elaine H.; Mennuti, Michael T.; Emanuel, Beverly S. (1988). "Molecular detection of a Yp/18 translocation in a 45,X holoprosencephalic male". Human Genetics. 80 (3). Springer Science and Business Media LLC: 219–223. doi:10.1007/bf01790089. ISSN0340-6717. PMID3192211.
Taine, L.; Goizet, C.; Wen, Z. Q.; Chateil, J. F.; Battin, J.; Saura, R.; Lacombe, D. (1997). "18p monosomy with midline defects and a de novo satellite identified by FISH". Annales de Génétique. 40 (3): 158–163. ISSN0003-3995. PMID9401105.
Kantaputra, Piranit N.; Limwongse, Chanin; Tochareontanaphol, Chintana; Mutirangura, Apiwat; Mevatee, Umnat; Praphanphoj, Verayuth (2006-09-25). "Contiguous gene syndrome of holoprosencephaly and hypotrichosis simplex: Association with an 18p11.3 deletion". American Journal of Medical Genetics Part A. 140A (23). Wiley: 2598–2602. doi:10.1002/ajmg.a.31386. ISSN1552-4825. PMID17001671.
Nazarenko, S. A.; Ostroverkhova, N. V.; Vasiljeva, E. O.; Nazarenko, L. P.; Puzyrev, V. P.; Malet, P.; Nemtseva, T. A. (1999-07-16). "Keratosis pilaris and ulerythema ophryogenes associated with an 18p deletion caused by a Y/18 translocation". American Journal of Medical Genetics. 85 (2): 179–182. doi:10.1002/(SICI)1096-8628(19990716)85:2<179::AID-AJMG14>3.0.CO;2-R. ISSN0148-7299. PMID10406673.
Klein, C.; Page, C.E.; LeWitt, P.; Gordon, M.F.; de Leon, D.; Awaad, Y.; Breakefield, X.O.; Brin, M.F.; Ozelius, L.J. (1999). "Genetic analysis of three patients with an 18p− syndrome and dystonia". Neurology. 52 (3). Ovid Technologies (Wolters Kluwer Health): 649–651. doi:10.1212/wnl.52.3.649. ISSN0028-3878. PMID10025808.
Nasir, Jamal; Frima, Nafsika; Pickard, Ben; Malloy, M. Pat; Zhan, Lingping; Grünewald, Richard (2006-06-06). "Unbalanced whole arm translocation resulting in loss of 18p in dystonia". Movement Disorders. 21 (6). Wiley: 859–863. doi:10.1002/mds.20846. ISSN0885-3185. PMID16541453.
Wang, Jin-Chen C.; Nemana, L.; Kou, S. Y.; Habibian, R.; Hajianpour, M. J. (1997-09-05). "Molecular cytogenetic characterization of 18;21 whole arm translocation associated with monosomy 18p". American Journal of Medical Genetics. 71 (4): 463–466. doi:10.1002/(SICI)1096-8628(19970905)71:4<463::AID-AJMG17>3.0.CO;2-E. PMID9286456.
Babovic-Vuksanovic, Dusica; Jenkins, S.C.; Ensenauer, R.; Newman, D.C.; Jalal, S.M. (2003-06-30). "Subtelomeric deletion of 18p in an adult with paranoid schizophrenia and mental retardation". American Journal of Medical Genetics Part A. 124A (3). Wiley: 318–322. doi:10.1002/ajmg.a.20391. ISSN1552-4825. PMID14708108.
Rigola, M.A.; Plaja, A.; Mediano, C.; Miro, R.; Egozcue, J.; Fuster, C. (2001). "Characterization of a heritable partial monosomy 18p by molecular and cytogenetic analysis". American Journal of Medical Genetics. 104 (1). Wiley: 37–41. doi:10.1002/ajmg.1584. ISSN0148-7299. PMID11746025.
de Ravel, Thomy J.L.; Thiry, Paul; Fryns, Jean-Pierre (2005). "Follow-up of adult males with chromosome 18p deletion". European Journal of Medical Genetics. 48 (2). Elsevier BV: 189–193. doi:10.1016/j.ejmg.2005.01.024. ISSN1769-7212. PMID16053911.
Hasi-Zogaj M, Sebold C, Heard P, Carter E, Soileau B, Hill A, Rupert D, Perry B, Atkinson S, O'Donnell L, Gelfond J, Lancaster J, Fox PT, Hale DE, Cody JD (2015). "A review of 18p deletions". Am J Med Genet C Semin Med Genet. 169 (3): 251–64. doi:10.1002/ajmg.c.31445. PMID26250845. S2CID20556694.
Faust, J.; habedank, M.; Nieuwenhuijsen, C. (1976). "The 18 p- syndrome". European Journal of Pediatrics. 123 (1). Springer Science and Business Media LLC: 59–66. doi:10.1007/bf00497681. ISSN0340-6997. PMID954771.
Wester, Ulrika; Bondeson, Marie-Louise; Edeby, Christina; Annerén, Göran (2006-05-11). "Clinical and molecular characterization of individuals with 18p deletion: A genotype–phenotype correlation". American Journal of Medical Genetics Part A. 140A (11). Wiley: 1164–1171. doi:10.1002/ajmg.a.31260. ISSN1552-4825. PMID16691587.
Grosso, S.; Pucci, L.; Di Bartolo, R.M.; Gobbi, G.; Bartalini, G.; Anichini, C.; Scarinci, R.; Balestri, M.; Farnetani, M.A.; Cioni, M.; Morgese, G.; Balestri, P. (2005). "Chromosome 18 aberrations and epilepsy: A review". American Journal of Medical Genetics Part A. 134A (1). Wiley: 88–94. doi:10.1002/ajmg.a.30575. ISSN1552-4825. PMID15690352.
Cohen, M. Michael (2006). "Holoprosencephaly: Clinical, anatomic, and molecular dimensions". Birth Defects Research Part A: Clinical and Molecular Teratology. 76 (9). Wiley: 658–673. doi:10.1002/bdra.20295. ISSN1542-0752. PMID17001700.
Münke, Maximilian; Page, David C.; Brown, Laura G.; Armson, B. Anthony; Zackai, Elaine H.; Mennuti, Michael T.; Emanuel, Beverly S. (1988). "Molecular detection of a Yp/18 translocation in a 45,X holoprosencephalic male". Human Genetics. 80 (3). Springer Science and Business Media LLC: 219–223. doi:10.1007/bf01790089. ISSN0340-6717. PMID3192211.
Taine, L.; Goizet, C.; Wen, Z. Q.; Chateil, J. F.; Battin, J.; Saura, R.; Lacombe, D. (1997). "18p monosomy with midline defects and a de novo satellite identified by FISH". Annales de Génétique. 40 (3): 158–163. ISSN0003-3995. PMID9401105.
Dharmaraj, P; Grueters, A (2006). "The management of thyrotoxicosis in a pre-pubertal child with 18p deletion syndrome". European Journal of Endocrinology. 155 (suppl_1): S145 –S147. doi:10.1530/eje.1.02274. ISSN0804-4643.
Kantaputra, Piranit N.; Limwongse, Chanin; Tochareontanaphol, Chintana; Mutirangura, Apiwat; Mevatee, Umnat; Praphanphoj, Verayuth (2006-09-25). "Contiguous gene syndrome of holoprosencephaly and hypotrichosis simplex: Association with an 18p11.3 deletion". American Journal of Medical Genetics Part A. 140A (23). Wiley: 2598–2602. doi:10.1002/ajmg.a.31386. ISSN1552-4825. PMID17001671.
Nazarenko, S. A.; Ostroverkhova, N. V.; Vasiljeva, E. O.; Nazarenko, L. P.; Puzyrev, V. P.; Malet, P.; Nemtseva, T. A. (1999-07-16). "Keratosis pilaris and ulerythema ophryogenes associated with an 18p deletion caused by a Y/18 translocation". American Journal of Medical Genetics. 85 (2): 179–182. doi:10.1002/(SICI)1096-8628(19990716)85:2<179::AID-AJMG14>3.0.CO;2-R. ISSN0148-7299. PMID10406673.
Klein, C.; Page, C.E.; LeWitt, P.; Gordon, M.F.; de Leon, D.; Awaad, Y.; Breakefield, X.O.; Brin, M.F.; Ozelius, L.J. (1999). "Genetic analysis of three patients with an 18p− syndrome and dystonia". Neurology. 52 (3). Ovid Technologies (Wolters Kluwer Health): 649–651. doi:10.1212/wnl.52.3.649. ISSN0028-3878. PMID10025808.
Nasir, Jamal; Frima, Nafsika; Pickard, Ben; Malloy, M. Pat; Zhan, Lingping; Grünewald, Richard (2006-06-06). "Unbalanced whole arm translocation resulting in loss of 18p in dystonia". Movement Disorders. 21 (6). Wiley: 859–863. doi:10.1002/mds.20846. ISSN0885-3185. PMID16541453.
Babovic-Vuksanovic, Dusica; Jenkins, S.C.; Ensenauer, R.; Newman, D.C.; Jalal, S.M. (2003-06-30). "Subtelomeric deletion of 18p in an adult with paranoid schizophrenia and mental retardation". American Journal of Medical Genetics Part A. 124A (3). Wiley: 318–322. doi:10.1002/ajmg.a.20391. ISSN1552-4825. PMID14708108.
Rigola, M.A.; Plaja, A.; Mediano, C.; Miro, R.; Egozcue, J.; Fuster, C. (2001). "Characterization of a heritable partial monosomy 18p by molecular and cytogenetic analysis". American Journal of Medical Genetics. 104 (1). Wiley: 37–41. doi:10.1002/ajmg.1584. ISSN0148-7299. PMID11746025.
de Ravel, Thomy J.L.; Thiry, Paul; Fryns, Jean-Pierre (2005). "Follow-up of adult males with chromosome 18p deletion". European Journal of Medical Genetics. 48 (2). Elsevier BV: 189–193. doi:10.1016/j.ejmg.2005.01.024. ISSN1769-7212. PMID16053911.
