Human Genome Epidemiology Literature Finder
Records 1 - 2 (of 2 Records) |
Query Trace: Hypertelorism and MID1[original query] |
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Duplication of the MID1 first exon in a patient with Opitz G/BBB syndrome. Human genetics 2003 1 112 (3): 249-54. Winter Jennifer, Lehmann Tanja, Suckow Vanessa, Kijas Zofia, Kulozik Andreas, Kalscheuer Vera, Hamel Ben, Devriendt Koen, Opitz John, Lenzner Steffen, Ropers Hans-Hilger, Schweiger Susa |
Hypospadias associated with hypertelorism, the mildest phenotype of Opitz syndrome. Journal of human genetics 2011 May 56 (5): 348-51. Zhang Xufeng, Chen Yougen, Zhao Shentiang, Markljung Ellen, Nordenskjöld Agne |
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- Page last updated:Apr 22, 2024
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