Discover open access scientific publications

Search, annotate, share and cite publications

Publications by Qing-wen Shan

Rare LPL Gene Missense Mutation in an Infant With Hypertriglyceridemia

Journal of Clinical Laboratory Analysis

Medical Laboratory Technology

Clinical Biochemistry

Occupational Health

English

Related publications

A Novel Missense Mutation in USP26 Gene Is Associated With Nonobstructive Azoospermia

Reproductive Sciences

English

Benign Infantile Epilepsy Mimicking Reflex Anoxic Seizures in an Infant With PRRT2 Gene Mutation

Indian Journal of Pediatrics

English

Transient Myeloproliferative Disorder in an Infant With PTPN11 Mutation

British Journal of Haematology

English

Missense Mutation in the USH2A Gene: Association With Recessive Retinitis Pigmentosa Without Hearing Loss

American Journal of Human Genetics

English

A Novel Missense Mutation T101N in the Melanocortin-4 Receptor Gene Associated With Obesity

Genetics and Molecular Research

Molecular Biology

English

A Novel APOC2 Gene Mutation Identified in a Chinese Patient With Severe Hypertriglyceridemia and Recurrent Pancreatitis

Lipids in Health and Disease

Clinical Biochemistry

English

A Novel Missense Mutation of F 9 Gene in Hemophilia B Patients

Journal of Blood Disorders & Transfusion

English

Identification of Missense Mutation (I12T) in the BSND Gene and Bioinformatics Analysis

Journal of Biomedicine and Biotechnology

English

GP56 Severe Hypercalcemic Crisis in an Infant With Idiopathic Infantile Hypercalcemia Caused by Mutation in CYP24A1 Gene

English