M. Germeshausen Et Al. , "Novel HAX1 mutations in patients with severe congenital neutropenia reveal isoform-dependent genotype-phenotype associations," BLOOD , vol.111, no.10, pp.4954-4957, 2008
Germeshausen, M. Et Al. 2008. Novel HAX1 mutations in patients with severe congenital neutropenia reveal isoform-dependent genotype-phenotype associations. BLOOD , vol.111, no.10 , 4954-4957.
Germeshausen, M., Grudzien, M., Zeidler, C., Abdollahpour, H., YETGİN, S., Rezaei, N., ... Ballmaier, M.(2008). Novel HAX1 mutations in patients with severe congenital neutropenia reveal isoform-dependent genotype-phenotype associations. BLOOD , vol.111, no.10, 4954-4957.
Germeshausen, Manuela Et Al. "Novel HAX1 mutations in patients with severe congenital neutropenia reveal isoform-dependent genotype-phenotype associations," BLOOD , vol.111, no.10, 4954-4957, 2008
Germeshausen, Manuela Et Al. "Novel HAX1 mutations in patients with severe congenital neutropenia reveal isoform-dependent genotype-phenotype associations." BLOOD , vol.111, no.10, pp.4954-4957, 2008
Germeshausen, M. Et Al. (2008) . "Novel HAX1 mutations in patients with severe congenital neutropenia reveal isoform-dependent genotype-phenotype associations." BLOOD , vol.111, no.10, pp.4954-4957.
@article{article, author={Manuela Germeshausen Et Al. }, title={Novel HAX1 mutations in patients with severe congenital neutropenia reveal isoform-dependent genotype-phenotype associations}, journal={BLOOD}, year=2008, pages={4954-4957} }