Qingliu Fu
5PUBLICATIONS
0CO-AUTHORS
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Publications (5)
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|Mar 24, 2021
Increased detection of primary carnitine deficiency through second-tier newborn genetic screening.Yiming Lin, Weifeng Zhang, Chenggang Huang
|Oct 14, 2020
Combined primary carnitine deficiency with neonatal intrahepatic cholestasis caused by citrin deficiency in a Chinese newborn.Yiming Lin, Weihua Lin, Yanru Chen
|Jun 19, 2019
Citrullinemia type I is associated with a novel splicing variant, c.773 + 4A > C, in ASS1: a case report and literature review.Yiming Lin, Hongzhi Gao, Bin Lu
|Jul 13, 2018
Mild clinical features of isolated methylmalonic acidemia associated with a novel variant in the MMAA gene in two Chinese siblings.Yiming Lin, Chunmei Lin, Weihua Lin
|Jan 07, 2018
A novel compound heterozygous variant identified in GLDC gene in a Chinese family with non-ketotic hyperglycinemia.Yiming Lin, Zhenzhu Zheng, Wenjia Sun
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