Dihydropyrimidine Dehydrogenase Deficiency in Two Malaysian Siblings with Abnormal MRI Findings-Reference-Cited by-同舟云学术

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Dihydropyrimidine Dehydrogenase Deficiency in Two Malaysian Siblings with Abnormal MRI Findings

Published:2014 Issue:6 Volume:5 Page:299-303
ISSN:1661-8769
Container-title:Molecular Syndromology
language:en
Short-container-title:Mol Syndromol

Author:

Chen Bee Chin,Mohd Rawi Rowani,Meinsma Rutger,Meijer Judith,Hennekam Raoul C.M.,van Kuilenburg André B.P.

Publisher

S. Karger AG

Subject

Genetics (clinical),Genetics

Cited by 10 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Review of Neurologic and Developmental Conditions Associated with Pediatric Dihydropyrimidine Dehydrogenase Deficiency;Advances in Molecular Pathology;2024-08

2. Metabolomic changes in children with autism;World Journal of Clinical Pediatrics;2024-06-09

3. Genetic Elucidation of Ultrasonography Fetal Anomalies in Children with Autism Spectrum Disorder;2023-08-09

4. Disorders of Beta and Gamma Amino Acids;Physician's Guide to the Diagnosis, Treatment, and Follow-Up of Inherited Metabolic Diseases;2022

5. Pharmacogenetic profiling of dihydropyrimidine dehydrogenase (DPYD) variants in the Indian population;The Journal of Gene Medicine;2020-11-20

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