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A case of de novo 18p deletion syndrome with panhypopituitarism
Aram Yang, Jinsup Kim, Sung Yoon Cho, Ji-Eun Lee, Hee-Jin Kim, Dong-Kyu Jin
Ann Pediatr Endocrinol Metab. 2019;24(1):60-63.   Published online March 31, 2019
DOI: https://doi.org/10.6065/apem.2019.24.1.60

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A case of de novo 18p deletion syndrome with panhypopituitarism
Annals of Pediatric Endocrinology & Metabolism. 2019;24(1):60-63   Crossref logo
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Myoclonus-dystonia in 18p deletion syndrome
Movement Disorders. 2010;26(3):560-561   Crossref logo
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Spectrum of Movement Disorders in 18p Deletion Syndrome
Movement Disorders Clinical Practice. 2018;6(1):70-73   Crossref logo
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Alternative surgical methods for ptosis in patients with 18p deletion syndrome
International Medical Case Reports Journal. 2017;Volume 10:97-98   Crossref logo
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Familial deletion 18p syndrome: case report
BMC Medical Genetics. 2006;7(1):   Crossref logo
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A retrospective CISS hybridization analysis of a case with de novo translocation t(18;22) resulting in an 18p-syndrome*
Clinical Genetics. 2008;43(6):318-320   Crossref logo
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A case of 18p deletion syndrome after blepharoplasty
International Medical Case Reports Journal. 2017;Volume 10:15-18   Crossref logo
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18p deletion syndrome with a 45, XY, t (14; 18) (p11;q11.2), -18, karyotype
Annales de Génétique. 2001;44(4):187-190   Crossref logo
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A case report of 46, XX, del (21)(q22) de novo deletion associated with Imerslund-Grasbeck syndrome
Clinical Genetics. 2008;50(4):248-250   Crossref logo
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Molecular characterization of a unique de novo 15q deletion associated with Prader-Willi syndrome and central visual impairment
Clinical Genetics. 2003;63(4):297-302   Crossref logo
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