Qingliu Fu

发表

Biochemical and molecular features of Chinese patients with glutaric acidemia type 1 detected through newborn screening

Yiming Lin, Wenjun Wang, Chunmei Lin, 2021, Orphanet Journal of Rare Diseases.

Expanded newborn screening for inherited metabolic disorders and genetic characteristics in a southern Chinese population.

Yiming Lin, Zhenzhu Zheng, Qingliu Fu, 2019, Clinica chimica acta; international journal of clinical chemistry.

Glutaric Acidemia type 1 with Atypical Acylcarnitine Profile During Newborn Screening

Yiming Lin, Wenjun Wang, Chunmei Lin, 2021 .

Increased primary carnitine deficiency detection through second-tier newborn genetic screening

Yiming Lin, Chunmei Lin, Qingliu Fu, 2021 .

Increased detection of primary carnitine deficiency through second-tier newborn genetic screening

Yiming Lin, Chunmei Lin, Qingliu Fu, 2021, Orphanet Journal of Rare Diseases.

Combined primary carnitine deficiency with neonatal intrahepatic cholestasis caused by citrin deficiency in a Chinese newborn

Yiming Lin, Chunmei Lin, Zhenzhu Zheng, 2020, BMC Pediatrics.

Three Novel and One Potential Hotspot CPT1A Variants in Chinese Patients With Carnitine Palmitoyltransferase 1A Deficiency

Yiming Lin, Chunmei Lin, Qingliu Fu, 2021, Frontiers in Pediatrics.

Mild clinical features of isolated methylmalonic acidemia associated with a novel variant in the MMAA gene in two Chinese siblings

Yiming Lin, Chunmei Lin, Zhenzhu Zheng, 2018, BMC medical genetics.

Newborn screening and genetic features of patients with hyperphenylalaninemia in a southern Chinese population.

Yiming Lin, Zhenzhu Zheng, Qingliu Fu, 2022, Clinica chimica acta; international journal of clinical chemistry.

Biochemical and genetic characteristics of patients with primary carnitine deficiency identified through newborn screening

Yiming Lin, Zhenzhu Zheng, Qingliu Fu, 2021, Orphanet Journal of Rare Diseases.

Clinical, biochemical, and genetic analysis of a Chinese Han pedigree with holocarboxylase synthetase deficiency: a case report

Min⁃ying Zheng, Yiming Lin, Zhenzhu Zheng, 2020, BMC Medical Genetics.

Incorporating second-tier genetic screening for multiple acyl-CoA dehydrogenase deficiency.

Yiming Lin, Qingliu Fu, Weilin Peng, 2022, Clinica chimica acta; international journal of clinical chemistry.

Clinical and genetic analysis of five Chinese patients with urea cycle disorders

Yiming Lin, Wenjun Wang, Zhenzhu Zheng, 2020, Molecular genetics & genomic medicine.

Newborn screening and molecular features of patients with multiple acyl-CoA dehydrogenase deficiency in Quanzhou, China

Yiming Lin, Chunmei Lin, Qingliu Fu, 2021, Journal of pediatric endocrinology & metabolism : JPEM.

Newborn screening for isovaleric acidemia in Quanzhou, China.

Yiming Lin, Zhenzhu Zheng, Qingliu Fu, 2020, Clinica chimica acta; international journal of clinical chemistry.

Biochemical, Clinical, and Genetic Characteristics of Short/Branched Chain Acyl-CoA Dehydrogenase Deficiency in Chinese Patients by Newborn Screening

Hongzhi Gao, Yiming Lin, Chunmei Lin, 2019, Front. Genet..

Clinical, biochemical and genetic analysis of Chinese patients with isobutyryl-CoA dehydrogenase deficiency.

Yiming Lin, Chunmei Lin, Zhenzhu Zheng, 2018, Clinica chimica acta; international journal of clinical chemistry.

A novel compound heterozygous variant identified in GLDC gene in a Chinese family with non-ketotic hyperglycinemia

Wenjia Sun, Yiming Lin, Zhenzhu Zheng, 2018, BMC Medical Genetics.

Citrullinemia type I is associated with a novel splicing variant, c.773 + 4A > C, in ASS1: a case report and literature review

Hongzhi Gao, Yiming Lin, Qingliu Fu, 2019, BMC Medical Genetics.

A novel compound heterozygous variant identified in GLDC gene in a Chinese family with non-ketotic hyperglycinemia

Wenjia Sun, Yiming Lin, Zhenzhu Zheng, 2018, BMC Medical Genetics.