J. Xu

Refinement of the spinal muscular atrophy locus by genetic and physical mapping.

G. Penchaszadeh, T. Carter, E. Vitale, 1995, American journal of human genetics.

Characterization of survival motor neuron (SMNT) gene deletions in asymptomatic carriers of spinal muscular atrophy.

T. Gilliam, G. Penchaszadeh, T. Carter, 1996, Human molecular genetics.

Interactions of allele E of the MC1R gene with FM and mutations in the MLPH gene cause the five-gray phenotype in the Anyi tile-like gray chicken.

M. Xie, X. Zhang, X. Li, 2016, Genetics and molecular research : GMR.

Null mutation of the murine ATP7B (Wilson disease) gene results in intracellular copper accumulation and late-onset hepatic nodular transformation.

T. Gilliam, S. Zeitlin, C. Mekios, 1999, Human molecular genetics.

Interactions of allele E of the MC1R gene with FM and mutations in the MLPH gene cause the five-gray phenotype in the Anyi tile-like gray chicken.

M. Xie, X. Li, J. Xu, 2016, Genetics and molecular research : GMR.