Dowsett, L., Lulis, L., Ficicioglu, C., & Cuddapah, S. (2017). Utility of Genetic Testing for Confirmation of Abnormal Newborn Screening in Disorders of Long-Chain Fatty Acids: A Missed Case of Carnitine Palmitoyltransferase 1A (CPT1A) Deficiency. Int J Neonatal Screen.
শিকাগো স্টাইলে সাইটেশনDowsett, Leah, Lauren Lulis, Can Ficicioglu, এবং Sanmati Cuddapah. "Utility of Genetic Testing for Confirmation of Abnormal Newborn Screening in Disorders of Long-Chain Fatty Acids: A Missed Case of Carnitine Palmitoyltransferase 1A (CPT1A) Deficiency." Int J Neonatal Screen 2017.
এমএলএ সাইটেশনDowsett, Leah, Lauren Lulis, Can Ficicioglu, এবং Sanmati Cuddapah. "Utility of Genetic Testing for Confirmation of Abnormal Newborn Screening in Disorders of Long-Chain Fatty Acids: A Missed Case of Carnitine Palmitoyltransferase 1A (CPT1A) Deficiency." Int J Neonatal Screen 2017.