Jinqun Liang

Severe forms of complete androgen insensitivity syndrome caused by a p.Q65X novel mutation in androgen receptor: Clinical manifestations, imaging findings and molecular genetics

Zhiqing Wang, Jianhui Jiang, Sisi Wei, 2019, Steroids.

Case Report: Successful Management of a 29-Day-Old Infant With Severe Hyperlipidemia From a Novel Homozygous Variant of GPIHBP1 Gene

Zhiqing Wang, Jianhui Jiang, Sisi Wei, 2022, Frontiers in Pediatrics.

Gray Matter Heterotopia, Mental Retardation, Developmental Delay, Microcephaly, and Facial Dysmorphisms in a Boy with Ring Chromosome 6: A 10-Year Follow-Up and Literature Review

Shu Liu, Zhiqing Wang, Jianhui Jiang, 2018, Cytogenetic and Genome Research.

Analysis of amino acids and acylcarnitines profiles in small, appropriate, and large for gestational age neonates

A. Yin, S. Wen, Jinqun Liang, 2020, The journal of maternal-fetal & neonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians.

Analysis of amino acids and acyl carnitine profiles in low birth weight, preterm, and small for gestational age neonates

A. Yin, Jianhui Jiang, Jinqun Liang, 2017, The journal of maternal-fetal & neonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians.

Two novel mutations in the glycine decarboxylase gene in a boy with classic nonketotic hyperglycinemia: case report.

Shu Liu, Zhiqing Wang, Jianhui Jiang, 2017, Archivos argentinos de pediatria.

Severe forms of Johanson-Blizzard syndrome caused by two novel compound heterozygous variants in UBR1: Clinical manifestations, imaging findings and molecular genetics.

Zhiqing Wang, Jianhui Jiang, Sisi Wei, 2020, Pancreatology : official journal of the International Association of Pancreatology (IAP) ... [et al.].