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Year | Number of Results |
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2007 | 1 |
2008 | 1 |
2014 | 2 |
2015 | 1 |
2024 | 0 |
PubMed (cited) for id: 619343
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Microarray analysis of 50 patients reveals the critical chromosomal regions responsible for 1p36 deletion syndrome-related complications.
Brain Dev. 2015 May;37(5):515-26. doi: 10.1016/j.braindev.2014.08.002. Epub 2014 Aug 27.
Brain Dev. 2015.
PMID: 25172301
Identification of critical regions and candidate genes for cardiovascular malformations and cardiomyopathy associated with deletions of chromosome 1p36.
Zaveri HP, Beck TF, Hernández-García A, Shelly KE, Montgomery T, van Haeringen A, Anderlid BM, Patel C, Goel H, Houge G, Morrow BE, Cheung SW, Lalani SR, Scott DA.
Zaveri HP, et al.
PLoS One. 2014 Jan 15;9(1):e85600. doi: 10.1371/journal.pone.0085600. eCollection 2014.
PLoS One. 2014.
PMID: 24454898
Free PMC article.
Item in Clipboard
A new case of proximal monosomy 1p36, extending the phenotype.
Rudnik-Schöneborn S, Zerres K, Häusler M, Lott A, Krings T, Schüler HM.
Rudnik-Schöneborn S, et al.
Am J Med Genet A. 2008 Aug 1;146A(15):2018-22. doi: 10.1002/ajmg.a.32405.
Am J Med Genet A. 2008.
PMID: 18627049
No abstract available.
Item in Clipboard
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.
Kang SH, et al.
Clin Genet. 2007 Oct;72(4):329-38. doi: 10.1111/j.1399-0004.2007.00876.x.
Clin Genet. 2007.
PMID: 17850629
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