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MeSH:(Genetic Diseases, Inborn)

1.Biochemical and clinical findings in the first two cases of glutaric aciduria type I in the Philippines

Fodra Esphie Grace D. ; Lanot Vanessa O. ; Balansay Lorena S. ; Chiong Mary Anne D.

Acta Medica Philippina 2011;45(4):70-72

4.Clinical and genetic analysis of a child with transcobalamin II deficiency.

Chunlan YANG ; Xiaodong WANG ; Chunjing WANG ; Xiaoling ZHANG ; Yue LI ; Yue YU ; Sixi LIU

Chinese Journal of Medical Genetics 2021;38(10):993-996

6.Gitelman's Syndrome Associated with Chondrocalcinosis.

Seung Taek SONG ; Yu Jeong LIM ; Joon Sung PARK ; Yoonah SONG ; Seunghun LEE ; Jeongim CHOI ; Jae Bum JUN

Journal of Rheumatic Diseases 2016;23(4):266-270

8.Inborn Errors of Metabolism in Korea.

Hong Jin LEE

Journal of the Korean Neurological Association 2004;22(1):1-10

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