PublisherDOIYearVolumeIssuePageTitleAuthor(s)Link
Annals of Pediatric Endocrinology & Metabolism10.6065/apem.2019.24.1.60201924160-63A case of de novo 18p deletion syndrome with panhypopituitarismAram Yang, Jinsup Kim, Sung Yoon Cho, Ji-Eun Lee, Hee-Jin Kim, Dong-Kyu Jinhttp://e-apem.org/upload/pdf/apem-2019-24-1-60.pdf, http://e-apem.org/journal/view.php?doi=10.6065/apem.2019.24.1.60, http://e-apem.org/upload/pdf/apem-2019-24-1-60.pdf
Movement Disorders Clinical Practice10.1002/mdc3.1270720186170-73Spectrum of Movement Disorders in 18p Deletion SyndromeDavid Crosiers, Bettina Blaumeiser, Gert Van Goethemhttps://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1002%2Fmdc3.12707, http://onlinelibrary.wiley.com/wol1/doi/10.1002/mdc3.12707/fullpdf
Movement Disorders10.1002/mds.234462010263560-561Myoclonus-dystonia in 18p deletion syndromeMarkus C. Kowarik, Sabine Langer, Corinna Keri, Bernhard Hemmer, Konrad Oexle, Juliane Winkelmannhttps://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1002%2Fmds.23446, https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1002%2Fmds.23446, http://onlinelibrary.wiley.com/wol1/doi/10.1002/mds.23446/fullpdf
BMC Medical Genetics10.1186/1471-2350-7-60200671Familial deletion 18p syndrome: case reportBruno Maranda, Nicole Lemieux, Emmanuelle Lemyrehttp://link.springer.com/content/pdf/10.1186/1471-2350-7-60.pdf, http://link.springer.com/article/10.1186/1471-2350-7-60/fulltext.html, http://link.springer.com/content/pdf/10.1186/1471-2350-7-60, https://link.springer.com/content/pdf/10.1186/1471-2350-7-60.pdf
International Medical Case Reports Journal10.2147/imcrj.s1239382017Volume 1015-18A case of 18p deletion syndrome after blepharoplastyLijuan Xu, Lvxian Wu, Qing Yuan, Zhigang Lv, Xueyan Jianghttps://www.dovepress.com/getfile.php?fileID=34427, https://www.dovepress.com/getfile.php?fileID=34427
International Medical Case Reports Journal10.2147/imcrj.s1337482017Volume 1097-98Alternative surgical methods for ptosis in patients with 18p deletion syndromeSang Beom Hanhttps://www.dovepress.com/getfile.php?fileID=35617, https://www.dovepress.com/getfile.php?fileID=35617
Clinical Genetics10.1111/j.1399-0004.1993.tb03827.x2008436318-320A retrospective CISS hybridization analysis of a case with de novo translocation t(18;22) resulting in an 18p-syndrome*Ion Voiculescu, Roland Toder, Elke Back, Peter Osswald, Werner Schempphttps://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1111%2Fj.1399-0004.1993.tb03827.x, http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1993.tb03827.x/fullpdf
Global Medical Genetics10.1055/s-0042-17432612022Presentation of an Infant with Chromosome 18p Deletion Syndrome and Asymmetric Septal HypertrophyAyca Kocaaga, Sevgi Yimeniciogluhttp://www.thieme-connect.de/products/ejournals/pdf/10.1055/s-0042-1743261.pdf
Clinical Neurology and Neurosurgery10.1016/j.clineuro.2009.07.013200911110880-882Characteristics of dystonia in the 18p deletion syndrome, including a new caseAnna G. Postma, Corien C. Verschuuren-Bemelmans, Klaas Kok, Teus van Laarhttps://api.elsevier.com/content/article/PII:S030384670900184X?httpAccept=text/xml, https://api.elsevier.com/content/article/PII:S030384670900184X?httpAccept=text/plain
Annales de Génétique10.1016/s0003-3995(01)01085-12001444187-19018p deletion syndrome with a 45, XY, t (14; 18) (p11;q11.2), -18, karyotypeVunditi Babu Rao, Lily Kerketta, Seema Korgaonkar, Kanjaksha Ghosh, Dipika Mohantyhttps://api.elsevier.com/content/article/PII:S0003399501010851?httpAccept=text/xml, https://api.elsevier.com/content/article/PII:S0003399501010851?httpAccept=text/plain