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The Cleft Palate-Craniofacial Journal : Official Publication of the American Cleft Palate-Craniofacial Association
|
June 20, 2015
IRF6 Sequencing in Interrupted Clefting
Sanmati R Cuddapah, Selma Kominek, John H Grant, et al.
Molecular Genetics and Metabolism
|
March 13, 2023
2-Methylglutaconic acid as a biomarker in routine urine organic acids leading to the diagnosis of glutaric acidemia type I in a low excretor
Parith Wongkittichote, Xinying Hong, Stephen R Master, et al.
JIMD Reports
|
September 13, 2023
Biochemical characterization of patients with dihydrolipoamide dehydrogenase deficiency
Parith Wongkittichote, Sanmati R Cuddapah, Stephen R Master, et al.
International Journal of Neonatal Screening
|
November 18, 2020
Newborn Screening for Pompe Disease: Pennsylvania Experience
Can Ficicioglu, Rebecca C Ahrens-Nicklas, Joshua Barch, et al.
JIMD Reports
|
January 13, 2025
Liver Transplant From a Deceased Donor With Cystinosis: A Case Report
Raeda Taj, Kim Ng, Sanmati R Cuddapah, et al.
Molecular Genetics and Metabolism Reports
|
November 24, 2022
Malate dehydrogenase 2 deficiency is an emerging cause of pediatric epileptic encephalopathy with a recognizable biochemical signature
Jessica R C Priestley, Lisa M Pace, Kuntal Sen, et al.
Pediatrics
|
June 1, 2022
Clinical Effectiveness of Telemedicine-Based Pediatric Genetics Care
Katherine M Szigety, Terrence B Crowley, Kimberly B Gaiser, et al.
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of 1
Search research articles
Search
Showing results (1-10 of 7) with videos related to
Sort By:
Page
of 1
The Cleft Palate-Craniofacial Journal : Official Publication of the American Cleft Palate-Craniofacial Association
|
June 20, 2015
IRF6 Sequencing in Interrupted Clefting
Sanmati R Cuddapah, Selma Kominek, John H Grant, et al.
Molecular Genetics and Metabolism
|
March 13, 2023
2-Methylglutaconic acid as a biomarker in routine urine organic acids leading to the diagnosis of glutaric acidemia type I in a low excretor
Parith Wongkittichote, Xinying Hong, Stephen R Master, et al.
JIMD Reports
|
September 13, 2023
Biochemical characterization of patients with dihydrolipoamide dehydrogenase deficiency
Parith Wongkittichote, Sanmati R Cuddapah, Stephen R Master, et al.
International Journal of Neonatal Screening
|
November 18, 2020
Newborn Screening for Pompe Disease: Pennsylvania Experience
Can Ficicioglu, Rebecca C Ahrens-Nicklas, Joshua Barch, et al.
JIMD Reports
|
January 13, 2025
Liver Transplant From a Deceased Donor With Cystinosis: A Case Report
Raeda Taj, Kim Ng, Sanmati R Cuddapah, et al.
Molecular Genetics and Metabolism Reports
|
November 24, 2022
Malate dehydrogenase 2 deficiency is an emerging cause of pediatric epileptic encephalopathy with a recognizable biochemical signature
Jessica R C Priestley, Lisa M Pace, Kuntal Sen, et al.
Pediatrics
|
June 1, 2022
Clinical Effectiveness of Telemedicine-Based Pediatric Genetics Care
Katherine M Szigety, Terrence B Crowley, Kimberly B Gaiser, et al.
Page
of 1