Cite
HARVARD Citation
van Koningsbruggen, S. et al. (2016). Complete and partial XYLT1 deletion in a patient with neonatal short limb skeletal dysplasia. American journal of medical genetics. 170 (2), pp. 510-514. [Online].
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van Koningsbruggen, S. et al. (2016). Complete and partial XYLT1 deletion in a patient with neonatal short limb skeletal dysplasia. American journal of medical genetics. 170 (2), pp. 510-514. [Online].