Brunner, H. Et Al. 2000. Homozygous null mutations of ROR2 tyrosine kinase cause the autosomal recessive form of Robinow syndrome.. AMERICAN JOURNAL OF HUMAN GENETICS , vol.67, no.4 , 40.

Brunner, H., Celli, J., Kayserili, H., van Beusekom, E., Brussel, W., Skovby, F., ... Kerr, B.(2000). Homozygous null mutations of ROR2 tyrosine kinase cause the autosomal recessive form of Robinow syndrome.. AMERICAN JOURNAL OF HUMAN GENETICS , vol.67, no.4, 40.

Brunner, HG Et Al. "Homozygous null mutations of ROR2 tyrosine kinase cause the autosomal recessive form of Robinow syndrome.," AMERICAN JOURNAL OF HUMAN GENETICS , vol.67, no.4, 40, 2000

Brunner, HG Et Al. "Homozygous null mutations of ROR2 tyrosine kinase cause the autosomal recessive form of Robinow syndrome.." AMERICAN JOURNAL OF HUMAN GENETICS , vol.67, no.4, pp.40, 2000

Brunner, H. Et Al. (2000) . "Homozygous null mutations of ROR2 tyrosine kinase cause the autosomal recessive form of Robinow syndrome.." AMERICAN JOURNAL OF HUMAN GENETICS , vol.67, no.4, p.40.

@article{article, author={HG Brunner Et Al. }, title={Homozygous null mutations of ROR2 tyrosine kinase cause the autosomal recessive form of Robinow syndrome.}, journal={AMERICAN JOURNAL OF HUMAN GENETICS}, year=2000, pages={40} }