APA
Pugliese M., Tingley K., Chow A., Pallone N., Smith M., Rahman A., Chakraborty P., Geraghty M. T., Irwin J., Tessier L., Nicholls S. G., Offringa M., Butcher N. J., Iverson R., Clifford T. J., Stockler S., Hutton B., Paik K., Tao J., Skidmore B., Coyle D., Duddy K., Dyack S., Greenberg C. R., Ghai S. J., Karp N., Korngut L., Kronick J., MacKenzie A., MacKenzie J., Maranda B., Mitchell J. J., Potter M., Prasad C., Schulze A., Sparkes R., Taljaard M., Trakadis Y., Walia J. & Potter B. K. (20210201). Outcomes in pediatric studies of medium-chain acyl-coA dehydrogenase (MCAD) deficiency and phenylketonuria (PKU): a review. : Orphanet journal of rare diseases.
Chicago
Pugliese Michael, Tingley Kylie, Chow Andrea, Pallone Nicole, Smith Maureen, Rahman Alvi, Chakraborty Pranesh, Geraghty Michael T, Irwin Julie, Tessier Laure, Nicholls Stuart G, Offringa Martin, Butcher Nancy J, Iverson Ryan, Clifford Tammy J, Stockler Sylvia, Hutton Brian, Paik Karen, Tao Jessica, Skidmore Becky, Coyle Doug, Duddy Kathleen, Dyack Sarah, Greenberg Cheryl R, Ghai Shailly Jain, Karp Natalya, Korngut Lawrence, Kronick Jonathan, MacKenzie Alex, MacKenzie Jennifer, Maranda Bruno, Mitchell John J, Potter Murray, Prasad Chitra, Schulze Andreas, Sparkes Rebecca, Taljaard Monica, Trakadis Yannis, Walia Jagdeep and Potter Beth K. 20210201. Outcomes in pediatric studies of medium-chain acyl-coA dehydrogenase (MCAD) deficiency and phenylketonuria (PKU): a review. : Orphanet journal of rare diseases.
Harvard
Pugliese M., Tingley K., Chow A., Pallone N., Smith M., Rahman A., Chakraborty P., Geraghty M. T., Irwin J., Tessier L., Nicholls S. G., Offringa M., Butcher N. J., Iverson R., Clifford T. J., Stockler S., Hutton B., Paik K., Tao J., Skidmore B., Coyle D., Duddy K., Dyack S., Greenberg C. R., Ghai S. J., Karp N., Korngut L., Kronick J., MacKenzie A., MacKenzie J., Maranda B., Mitchell J. J., Potter M., Prasad C., Schulze A., Sparkes R., Taljaard M., Trakadis Y., Walia J. and Potter B. K. (20210201). Outcomes in pediatric studies of medium-chain acyl-coA dehydrogenase (MCAD) deficiency and phenylketonuria (PKU): a review. : Orphanet journal of rare diseases.
MLA
Pugliese Michael, Tingley Kylie, Chow Andrea, Pallone Nicole, Smith Maureen, Rahman Alvi, Chakraborty Pranesh, Geraghty Michael T, Irwin Julie, Tessier Laure, Nicholls Stuart G, Offringa Martin, Butcher Nancy J, Iverson Ryan, Clifford Tammy J, Stockler Sylvia, Hutton Brian, Paik Karen, Tao Jessica, Skidmore Becky, Coyle Doug, Duddy Kathleen, Dyack Sarah, Greenberg Cheryl R, Ghai Shailly Jain, Karp Natalya, Korngut Lawrence, Kronick Jonathan, MacKenzie Alex, MacKenzie Jennifer, Maranda Bruno, Mitchell John J, Potter Murray, Prasad Chitra, Schulze Andreas, Sparkes Rebecca, Taljaard Monica, Trakadis Yannis, Walia Jagdeep and Potter Beth K. Outcomes in pediatric studies of medium-chain acyl-coA dehydrogenase (MCAD) deficiency and phenylketonuria (PKU): a review. : Orphanet journal of rare diseases. 20210201.