Cite
HARVARD Citation
Roifman, M. et al. (n.d.). De novo WNT5A‐associated autosomal dominant Robinow syndrome suggests specificity of genotype and phenotype. Clinical genetics. pp. 34-41. [Online].
This is an interim version of our Electronic Legal Deposit Catalogue-eJournals and eBooks while we continue to recover from a cyber-attack.
Roifman, M. et al. (n.d.). De novo WNT5A‐associated autosomal dominant Robinow syndrome suggests specificity of genotype and phenotype. Clinical genetics. pp. 34-41. [Online].