Taylan, F. Et Al. 2016. Spondyloocular Syndrome: Novel Mutations in XYLT2 Gene and Expansion of the Phenotypic Spectrum. JOURNAL OF BONE AND MINERAL RESEARCH , vol.31, no.8 , 1577-1585.

Taylan, F., Costantini, A., Coles, N., PEKKINEN, M., Heon, E., Siklar, Z., ... Berberoglu, M.(2016). Spondyloocular Syndrome: Novel Mutations in XYLT2 Gene and Expansion of the Phenotypic Spectrum. JOURNAL OF BONE AND MINERAL RESEARCH , vol.31, no.8, 1577-1585.

Taylan, Fulya Et Al. "Spondyloocular Syndrome: Novel Mutations in XYLT2 Gene and Expansion of the Phenotypic Spectrum," JOURNAL OF BONE AND MINERAL RESEARCH , vol.31, no.8, 1577-1585, 2016

Taylan, Fulya Et Al. "Spondyloocular Syndrome: Novel Mutations in XYLT2 Gene and Expansion of the Phenotypic Spectrum." JOURNAL OF BONE AND MINERAL RESEARCH , vol.31, no.8, pp.1577-1585, 2016

Taylan, F. Et Al. (2016) . "Spondyloocular Syndrome: Novel Mutations in XYLT2 Gene and Expansion of the Phenotypic Spectrum." JOURNAL OF BONE AND MINERAL RESEARCH , vol.31, no.8, pp.1577-1585.

@article{article, author={Fulya Taylan Et Al. }, title={Spondyloocular Syndrome: Novel Mutations in XYLT2 Gene and Expansion of the Phenotypic Spectrum}, journal={JOURNAL OF BONE AND MINERAL RESEARCH}, year=2016, pages={1577-1585} }