HuGE Literature Finder
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Distinct DNA methylation profiles in subtypes of orofacial cleft. Clinical epigenetics 2017 6 9 63. Sharp Gemma C, Ho Karen, Davies Amy, Stergiakouli Evie, Humphries Kerry, McArdle Wendy, Sandy Jonathan, Davey Smith George, Lewis Sarah J, Relton Caroline |
A candidate gene approach to identify modifiers of the palatal phenotype in 22q11.2 deletion syndrome patients. International journal of pediatric otorhinolaryngology 2013 Jan 77 (1): 123-7. Widdershoven Josine C C, Bowser Mark, Sheridan Molly B, McDonald-McGinn Donna M, Zackai Elaine H, Solot Cynthia B, Kirschner Richard E, Beemer Frits A, Morrow Bernice E, Devoto Marcella, Emanuel Beverly |
Overt cleft palate phenotype and TBX1 genotype correlations in velo-cardio-facial/DiGeorge/22q11.2 deletion syndrome patients. American journal of medical genetics. Part A 2012 Oct . Herman SB, Guo T, McGinn DM, Blonska A, Shanske AL, Bassett AS, Chow EW, Bowser M, Sheridan M, Beemer F, Devriendt K, Swillen A, Breckpot J, Digilio MC, Marino B, Dallapiccola B, Carpenter C, Zheng X, Johnson J, Chung J, Higgins AM, Philip N, Simon T, Coleman K, Heine-Suner D, Rosell J, Kates W, Devoto M, Zackai E, Wang T, Shprintzen R, Emanuel BS, Morrow BE |
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