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Publications by Yang-yang Wu
Rare LPL Gene Missense Mutation in an Infant With Hypertriglyceridemia
Journal of Clinical Laboratory Analysis
Allergy
Immunology
Biochemistry
Public Health
Medical Laboratory Technology
Clinical Biochemistry
Hematology
Microbiology
Environmental
Occupational Health
Related publications
A Novel Missense Mutation in USP26 Gene Is Associated With Nonobstructive Azoospermia
Reproductive Sciences
Gynecology
Obstetrics
Benign Infantile Epilepsy Mimicking Reflex Anoxic Seizures in an Infant With PRRT2 Gene Mutation
Indian Journal of Pediatrics
Child Health
Pediatrics
Perinatology
Transient Myeloproliferative Disorder in an Infant With PTPN11 Mutation
British Journal of Haematology
Hematology
Missense Mutation in the USH2A Gene: Association With Recessive Retinitis Pigmentosa Without Hearing Loss
American Journal of Human Genetics
Genetics
A Novel Missense Mutation T101N in the Melanocortin-4 Receptor Gene Associated With Obesity
Genetics and Molecular Research
Medicine
Genetics
Molecular Biology
A Novel APOC2 Gene Mutation Identified in a Chinese Patient With Severe Hypertriglyceridemia and Recurrent Pancreatitis
Lipids in Health and Disease
Biochemistry
Endocrinology
Clinical Biochemistry
Metabolism
Diabetes
A Novel Missense Mutation of F 9 Gene in Hemophilia B Patients
Journal of Blood Disorders & Transfusion
Identification of Missense Mutation (I12T) in the BSND Gene and Bioinformatics Analysis
Journal of Biomedicine and Biotechnology
GP56 Severe Hypercalcemic Crisis in an Infant With Idiopathic Infantile Hypercalcemia Caused by Mutation in CYP24A1 Gene