Citations for
1ATAD5, C17orf79, CENTA2, CRLF3, EVI2A, EVI2B, NF1, NF1DEL, OMG, RNF135, SUZ12, TEFM, UTP6
Mutations in RNF135, a gene within the NF1 microdeletion region, cause phenotypic abnormalities including overgrowth.
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.
Nat Genet 39(8):963-5. Epub 2007 Jul 15. 2007
2ATAD5, LRRC37B, NF1, NF1DEL, RNF135
Molecular characterization and gene content of breakpoint boundaries in patients with neurofibromatosis type 1 with 17q11.2 microdeletions.
Jenne DE, Tinschert S, Reimann H, Lasinger W, Thiel G, Hameister H,Kehrer-Sawatzki H.
Am J Hum Genet 69(3):516-27. Epub 2001 Jul 20. 2001