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Publications by Weizhen Xu
RAD21 Mutations Cause a Human Cohesinopathy
American Journal of Human Genetics
Genetics
Acquisition of Plasmid With Carbapenem-Resistance Gene blaKPC2 in Hypervirulent Klebsiella Pneumoniae, Singapore
Emerging Infectious Diseases
Epidemiology
Infectious Diseases
Microbiology
Related publications
Reply to Mazzeu: Human Mutations inRYKMight Cause Robinow Syndrome
Journal of Biological Chemistry
Biochemistry
Cell Biology
Molecular Biology
Human Mutations in NDE1 Cause Extreme Microcephaly With Lissencephaly
American Journal of Human Genetics
Genetics
Mutations in the Human TBX4 Gene Cause Small Patella Syndrome
American Journal of Human Genetics
Genetics
Mutations in RAD21 Disrupt Regulation of APOB in Patients With Chronic Intestinal Pseudo-Obstruction
Gastroenterology
Hepatology
Gastroenterology
ACTN1 Mutations Cause Congenital Macrothrombocytopenia
American Journal of Human Genetics
Genetics
LRIG2 Mutations Cause Urofacial Syndrome
American Journal of Human Genetics
Genetics
Mutations in SOX2 Cause Anophthalmia
Nature Genetics
Genetics
NPMc+ Cooperates With Flt3/Itd Mutations to Cause Acute Leukemia Recapitulating Human Disease
Experimental Hematology
Cancer Research
Genetics
Hematology
Molecular Biology
Cell Biology
TNXB Mutations Can Cause Vesicoureteral Reflux
Journal of the American Society of Nephrology : JASN
Medicine
Nephrology