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  • Search Condition : Filter (MeSH = Heterozygote*)
Species Resource Title
Human and Animal Cells NHSF46(RCB0162) , GM2-1TKB(RCB0697) Compound heterozygosity with two novel mutations in the HEXB gene produces adult Sandhoff disease presenting as a motor neuron disease phenotype.
Human and Animal Cells CHO-K1 Long QT syndrome and associated gene mutation carriers in Japanese children: results from ECG screening examinations.
Mice RBRC02227 Compound heterozygous mutations in RIPPLY2 associated with vertebral segmentation defects.
C.intestinalis / (O.japonicus) Wild C. int Sustained heterozygosity across a self-incompatibility locus in an inbred ascidian.