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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Jan 25, 2025. (Total: 235671Documents)
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Records 1 - 2 (of 2 Records)

Query Trace: Cleft Palate and TBX1[original query]
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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