| 1 | ATAD5, C17orf79, CENTA2, CRLF3, EVI2A, EVI2B, NF1, NF1DEL, OMG, RNF135, SUZ12, TEFM, UTP6
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| Mutations in RNF135, a gene within the NF1 microdeletion region, cause phenotypic abnormalities including overgrowth.
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| Douglas J, Cilliers D, Coleman K, Tatton-Brown K, Barker K, Bernhard B, Burn J, Huson S, Josifova D, Lacombe D, Malik M, Mansour S, Reid E, Cormier-Daire V, Cole T; Childhood Overgrowth Collaboration, Rahman N.
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| Nat Genet 39(8):963-5. Epub 2007 Jul 15. 2007
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| 2 | ATAD5, LRRC37B, NF1, NF1DEL, RNF135
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| Molecular characterization and gene content of breakpoint boundaries in patients with neurofibromatosis type 1 with 17q11.2 microdeletions.
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| Jenne DE, Tinschert S, Reimann H, Lasinger W, Thiel G, Hameister H,Kehrer-Sawatzki H.
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| Am J Hum Genet 69(3):516-27. Epub 2001 Jul 20. 2001
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