| 1 | DEL15Q14
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| Complex chromosome rearrangements related 15q14 microdeletion plays a relevant role in phenotype expression and delineates a novel recurrent syndrome.
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| Roberti MC, Surace C, Digilio MC, D'Elia G, Sirleto P, Capolino R, Lombardo A, Tomaiuolo AC, Petrocchi S, Angioni A.
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| Orphanet J Rare Dis 6:17.
2011
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| 2 | DEL15Q14, MEIS2
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| Further evidence for the possible role of MEIS2 in the development of cleft palate and cardiac septum.
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| Crowley MA, Conlin LK, Zackai EH, Deardorff MA, Thiel BD, Spinner NB.
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| Am J Med Genet A 152A(5):1326-7. No abstract available. PMID: 20425846 2010
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| 3 | DEL15Q14
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| 15q13q14 deletions: phenotypic characterization and molecular delineation by comparative genomic hybridization.
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| Brunetti-Pierri N, Sahoo T, Frioux S, Chinault C, Zascavage R, Cheung SW, Peters S, Shinawi M.
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| Am J Med Genet A 146A(15):1933-41. 2008
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| 4 | DEL15Q14
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| A 5.6-Mb deletion in 15q14 in a boy with speech and language disorder, cleft palate, epilepsy, a ventricular septal defect, mental retardation and developmental delay.
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| Chen CP, Lin SP, Tsai FJ, Chern SR, Lee CC, Wang W.
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| Eur J Med Genet 51(4):368-72. Epub 2008 Mar 29.
2008
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| 5 | DEL15Q14
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| Characterization of a 5.3 Mb deletion in 15q14 by comparative genomic hybridization using a whole genome tiling path BAC array in a girl with heart defect, cleft palate, and developmental delay.
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| Erdogan F, Ullmann R, Chen W, Schubert M, Adolph S, Hultschig C, Kalscheuer V, Ropers HH, Spaich C, Tzschach A.
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| Am J Med Genet A 143(2):172-8. 2007
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| 6 | DEL15Q14
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| Cytogenetic and molecular cytogenetic studies of a case of interstitial deletion of proximal 15q.
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| Tonk V, Wyandt HE, Osella P, Skare J, Wu BL, Haddad B, Milunsky A.
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| Clin Genet 48(3):151-5. Review. 1995
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