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European Journal of Medical Genetics|May 15, 2012
Chromosome 2p15p16.1 microdeletion syndrome: 2.5 Mb deletion in a patient with renal anomalies, intractable seizures and a choledochal cystVishwanathan Hucthagowder, Ta-Chiang Liu, Alex R Paciorkowski, et al.American Journal of Medical Genetics. Part A|September 15, 2015
Familial recurrences of FOXG1-related disorder: Evidence for mosaicismKelly Q McMahon, Apostolos Papandreou, Mandy Ma, et al.Peerj|November 26, 2020
Genome-wide identification and analysis of the thiolase family in insectsShou-Min FangDevelopmental Medicine and Child Neurology|March 31, 2018
Phenotypes, genotypes, and the management of paroxysmal movement disordersLaura Silveira-Moriyama, Stjepana Kovac, Manju A Kurian, et al.American Journal of Medical Genetics. Part A|May 25, 2013
Deletion 16p13.11 uncovers NDE1 mutations on the non-deleted homolog and extends the spectrum of severe microcephaly to include fetal brain disruptionAlex R Paciorkowski, Kim Keppler-Noreuil, Luther Robinson, et al.Chinese Journal of Integrative Medicine|July 1, 2011
Research progress on the standardization of Chinese Tuina therapy: a short reviewLei Fang, Min FangAlternative Therapies in Health and Medicine|August 13, 2023
Glycemic Control of Type 2 Diabetes with the Chinese Metabolic Management Center and eKTANGFeifei Lai, Min FangJournal of Inequalities and Applications|February 3, 2018
Robust optimization model for uncertain multiobjective linear programsLei Wang, Min FangScience China. Life Sciences|May 2, 2013
Immunosenescence and age-related viral diseasesYongchao Ma, Min FangSheng Wu Gong Cheng Xue Bao = Chinese Journal of Biotechnology|May 24, 2024
[Advances of monoclonal antibodies and analysis of marketed antibody drugs]Guanglei Gu, Min FangPageof 157