| 1 | RAI1, SMS, SMS-REPD, SMS-REPM, SMS-REPP
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| Refinement of the Smith-Magenis syndrome critical region to approximately 950kb and assessment of 17p11.2 deletions. Are all deletions created equally?
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| Vlangos CN, Yim DK, Elsea SH.
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| Mol Genet Metab 79(2):134-41. 2003
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| 2 | DUP17P11, SMS, SMS-REPD, SMS-REPM, SMS-REPP
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| Genetic proof of unequal meiotic crossovers in reciprocal deletion and duplication of 17p11.2.
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| Shaw CJ, Bi W, Lupski JR.
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| Am J Hum Genet 71(5):1072-81. Epub 2002 Oct 9. 2002
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| 3 | ALKBH5, ATPAF2, C17orf39, COPS3, LLGL1, MED9, MIEF2, RAI1, RASD1, SMCR, SMCR2, SMCR3, SMCR4, SMCR5, SMCR6, SMCR8, SMCR9, SMS, SMS-REPD, SMS-REPM, SMS-REPP, TOM1L2
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| Genes in a refined Smith-Magenis syndrome critical deletion interval on chromosome 17p11.2 and the syntenic region of the mouse.
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| Bi W, Yan J, Stankiewicz P, Park SS, Walz K, Boerkoel CF, Potocki L, Shaffer LG, Devriendt K, Nowaczyk MJ, Inoue K, Lupski JR.
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| Genome Res 12(5):713-28. 2002
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| 4 | EEF1A3, RASD1, SMS, SMS-REPD, SMS-REPM, SMS-REPP, SRP68, ZBTB20, ZNF287
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| Genomic organisation of the approximately 1.5 Mb Smith-Magenis syndrome critical interval: transcription map, genomic contig, and candidate gene analysis.
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| Lucas RE, Vlangos CN, Das P, Patel PI, Elsea SH.
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| Eur J Hum Genet 9(12):892-902. 2001
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