Human Genome Epidemiology Literature Finder
Records 1 - 2 (of 2 Records) |
Query Trace: TUBGCP4[original query] |
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Rare missense TUBGCP5 gene variant in a patient with primary microcephaly. European journal of medical genetics 2018 12 62 (12): 103598. Maver Aleš, ?uturilo Goran, Kovanda Anja, Mileti? Aleksandra, Peterlin Bor |
Genotype Phenotype Correlation and Variability in Microcephaly Associated With Chorioretinopathy or Familial Exudative Vitreoretinopathy. Investigative ophthalmology & visual science 2020 11 61 (13): 2. Shurygina Maria F, Simonett Joseph M, Parker Maria A, Mitchell Amanda, Grigorian Florin, Lifton Jacob, Nagiel Aaron, Shpak Alexander A, Dadali Elena L, Mishina Irina A, Weleber Richard G, Yang Paul, Pennesi Mark |
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- Page last updated:Apr 22, 2024
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