Cite
Bi-allelic Pathogenic Variants in HS2ST1 Cause a Syndrome Characterized by Developmental Delay and Corpus Callosum, Skeletal, and Renal Abnormalities
MLA
Katharina Steindl, et al. Bi-Allelic Pathogenic Variants in HS2ST1 Cause a Syndrome Characterized by Developmental Delay and Corpus Callosum, Skeletal, and Renal Abnormalities. Dec. 2020. EBSCOhost, https://doi.org/10.1016/j.ajhg.2020.10.007.
APA
Katharina Steindl, Peter Meinecke, Catherine L.R. Merry, Leonie von Elsner, Petra J. G. Zwijnenburg, Kerstin Kutsche, Marjan M. Weiss, Anita Rauch, Malik Alawi, Pauline E. Schneeberger, Emma L. Barker, Iris Marquardt, & Pascal Joset. (2020). Bi-allelic Pathogenic Variants in HS2ST1 Cause a Syndrome Characterized by Developmental Delay and Corpus Callosum, Skeletal, and Renal Abnormalities. https://doi.org/10.1016/j.ajhg.2020.10.007
Chicago
Katharina Steindl, Peter Meinecke, Catherine L.R. Merry, Leonie von Elsner, Petra J. G. Zwijnenburg, Kerstin Kutsche, Marjan M. Weiss, et al. 2020. “Bi-Allelic Pathogenic Variants in HS2ST1 Cause a Syndrome Characterized by Developmental Delay and Corpus Callosum, Skeletal, and Renal Abnormalities,” December. doi:10.1016/j.ajhg.2020.10.007.