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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: Hypertelorism and MID1[original query]
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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