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23. Electroclinical features of epilepsy associated with 1p36 deletion syndrome: A review. Greco M; Ferrara P; Farello G; Striano P; Verrotti A Epilepsy Res; 2018 Jan; 139():92-101. PubMed ID: 29212048 [TBL] [Abstract][Full Text] [Related]
24. Monosomy 1p36 deletion syndrome. Gajecka M; Mackay KL; Shaffer LG Am J Med Genet C Semin Med Genet; 2007 Nov; 145C(4):346-56. PubMed ID: 17918734 [TBL] [Abstract][Full Text] [Related]
25. Further delineation of novel 1p36 rearrangements by array-CGH analysis: narrowing the breakpoints and clarifying the "extended" phenotype. Giannikou K; Fryssira H; Oikonomakis V; Syrmou A; Kosma K; Tzetis M; Kitsiou-Tzeli S; Kanavakis E Gene; 2012 Sep; 506(2):360-8. PubMed ID: 22766398 [TBL] [Abstract][Full Text] [Related]
26. Narrowing the deleted region associated with the 15q21 syndrome. Pramparo T; Mattina T; Gimelli S; Liehr T; Zuffardi O Eur J Med Genet; 2005; 48(3):346-52. PubMed ID: 16179230 [TBL] [Abstract][Full Text] [Related]
27. Chromothripsis with at least 12 breaks at 1p36.33-p35.3 in a boy with multiple congenital anomalies. Gamba BF; Richieri-Costa A; Costa S; Rosenberg C; Ribeiro-Bicudo LA Mol Genet Genomics; 2015 Dec; 290(6):2213-6. PubMed ID: 26040972 [TBL] [Abstract][Full Text] [Related]
28. Clinical features of chromosome 22q11.2 microdeletion syndrome in 208 Chilean patients. Repetto GM; Guzmán ML; Puga A; Calderón JF; Astete CP; Aracena M; Arriaza M; Aravena T; Sanz P Clin Genet; 2009 Nov; 76(5):465-70. PubMed ID: 19737282 [TBL] [Abstract][Full Text] [Related]
29. Revisit on a distinctive chromosome 1p36 deletion syndrome: report of one case and review of the English literature. Lee ML; Tsao LY; Wang BT; Lee MH; Chiu IS Int J Cardiol; 2004 Sep; 96(3):477-80. PubMed ID: 15301904 [No Abstract] [Full Text] [Related]
30. [Prenatal diagnosis of two fetuses with chromosome 1p36 deletion syndrome]. Ji X; Hu H; Wang Y; Liang D; Luo C; Meng L; Zhou J; Cao L; Ma D; Hu P; Xu Z Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2017 Dec; 34(6):853-856. PubMed ID: 29188615 [TBL] [Abstract][Full Text] [Related]
31. A girl with 1p36 deletion syndrome and congenital fiber type disproportion myopathy. Okamoto N; Toribe Y; Nakajima T; Okinaga T; Kurosawa K; Nonaka I; Shimokawa O; Matsumoto N J Hum Genet; 2002; 47(10):556-9. PubMed ID: 12376748 [TBL] [Abstract][Full Text] [Related]
32. Multiple causes of apnea in 1p36 deletion syndrome include seizures. Kanabar G; Boyd S; Schugal A; Bhate S Seizure; 2012 Jun; 21(5):402-6. PubMed ID: 22425009 [TBL] [Abstract][Full Text] [Related]
33. A patient with monosomy 1p36, atypical features and phenotypic similarities with Cantu syndrome. Tan TY; Bankier A; Slater HR; Northrop EL; Zacharin M; Savarirayan R Am J Med Genet A; 2005 Dec; 139(3):216-20. PubMed ID: 16278903 [TBL] [Abstract][Full Text] [Related]
34. Identification of proximal 1p36 deletions using array-CGH: a possible new syndrome. Kang SH; Scheffer A; Ou Z; Li J; Scaglia F; Belmont J; Lalani SR; Roeder E; Enciso V; Braddock S; Buchholz J; Vacha S; Chinault AC; Cheung SW; Bacino CA Clin Genet; 2007 Oct; 72(4):329-38. PubMed ID: 17850629 [TBL] [Abstract][Full Text] [Related]
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36. Partial duplication 4q and deletion 1p36 in monozygotic twins with discordant phenotypes. Angle B; Yen F; Hersh JH; Gowans G; Barch M Am J Med Genet; 2002 Aug; 111(3):307-12. PubMed ID: 12210328 [TBL] [Abstract][Full Text] [Related]
37. The del(2)(q32.2q33) deletion syndrome defined by clinical and molecular characterization of four patients. Van Buggenhout G; Van Ravenswaaij-Arts C; Mc Maas N; Thoelen R; Vogels A; Smeets D; Salden I; Matthijs G; Fryns JP; Vermeesch JR Eur J Med Genet; 2005; 48(3):276-89. PubMed ID: 16179223 [TBL] [Abstract][Full Text] [Related]
38. Prenatal diagnosis of a de novo interstitial deletion of chromosome 20q12 in a fetus with complex congenital heart defects, corpus callosum agenesis and intrauterine growth restriction. Lin YH; Chen CP; Chen TC; Hsu CS; Chou SY; Chien SC Taiwan J Obstet Gynecol; 2011 Dec; 50(4):528-30. PubMed ID: 22212331 [No Abstract] [Full Text] [Related]
39. The Neuropathology of 1p36 Deletion Syndrome: An Autopsy Case Series. Conway KS; Ghafoor F; Gottschalk AC; Laakman J; Eigsti RL; Nashelsky M; Blau J; Hefti MM J Neuropathol Exp Neurol; 2021 Sep; 80(9):856-860. PubMed ID: 34363665 [TBL] [Abstract][Full Text] [Related]
40. Development of a comparative genomic hybridization microarray and demonstration of its utility with 25 well-characterized 1p36 deletions. Yu W; Ballif BC; Kashork CD; Heilstedt HA; Howard LA; Cai WW; White LD; Liu W; Beaudet AL; Bejjani BA; Shaw CA; Shaffer LG Hum Mol Genet; 2003 Sep; 12(17):2145-52. PubMed ID: 12915473 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]