Publication | Closed Access
A gene for Waardenburg Syndrome type 2 maps close to the human homologue of the microphthalmia gene at chromosome 3p12–p14.1
168
Citations
24
References
1994
Year
Developmental BiologyMendelian DisorderCytogeneticsGenetic DisorderGeneticsMolecular BiologyChromosome 3P12–p14.1Molecular GeneticsDisease Gene IdentificationMedicineHuman HomologueMicrophthalmia Gene
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