Haifeng Liu

发表

Clinical and genetic analysis of 2 rare cases of Wiskott–Aldrich syndrome from Chinese minorities

Yanchun Wang, Yangfang Li, Lvyan Tao, 2021, Medicine.

Two novel Mutations of the LPL Gene in two Chinese family cases with Familial Chylomicronemia Syndrome.

Yu Zhang, Li Li, Lin Zhou, 2021, Clinica chimica acta; international journal of clinical chemistry.

Relationship between Glycemic Load and Blood Lipid Level in Hospitalized Adult Chinese

Hui Li, L. Li, Haifeng Liu, 2015, Iranian journal of public health.

A 13.42-kb tandem duplication at the ASIP locus is strongly associated with the depigmentation phenotype of non-classic Swiss markings in goats

Jiazhong Guo, Li Li, Linjie Wang, 2022, BMC genomics.

A novel mutation of the ITGB2 gene in a Chinese Zhuang minority patient with leukocyte adhesion deficiency type 1 and glucose-6-phosphate dehydrogenase deficiency.

Y. Zhang, Yanchun Wang, Yu Zhang, 2019, Gene.

A novel homozygous mutation of the PCNT gene in a Chinese patient with microcephalic osteodysplastic primordial dwarfism type II

Yu Zhang, Li Li, Na Tao, 2021, Molecular genetics & genomic medicine.

Preparation, characterization and alcoholic liver injury protective effects of algal oligosaccharides from Gracilaria lemaneiformis.

R. Zeng, Yanping Hou, Min Jin, 2017, Food research international.

A 13.42-kb tandem duplication at the ASIP locus is strongly associated with the depigmentation phenotype of non-classic Swiss markings in goats

Jiazhong Guo, Li Li, Linjie Wang, 2022, BMC Genomics.

A novel embolic middle cerebral artery occlusion model induced by thrombus formed in common carotid artery in rat

G. Du, Jun-Ke Song, Yinzhong Ma, 2015, Journal of the Neurological Sciences.

Clinical and genetic analysis of 2 rare cases of Wiskott–Aldrich syndrome from Chinese minorities

Yanchun Wang, Lvyan Tao, Haifeng Liu, 2021, Medicine.