Publication | Open Access
Mutations in LRP5 or FZD4 Underlie the Common Familial Exudative Vitreoretinopathy Locus on Chromosome 11q
370
Citations
41
References
2004
Year
Fzd4 UnderlieChromosome 11QMendelian DisorderGenetic DisorderGeneticsPathologyMolecular GeneticsMedical GeneticsDisease Gene IdentificationMedicineClinical Genetics
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