Lv11
90 积分 2025-05-21 加入
Differential genetic analysis of ectrodactyly in a Fanconi anemia pedigree with FANCA mutations
2小时前
待确认
A first large study of whole-exome sequencing (WES) in 489 patients with suspected rare genetic disorders at a tertiary centre in Malaysia
19天前
已关闭
Identification of novel genes involved in pediatric congenital heart disease using trio-based whole genome sequencing
2个月前
已完结
Clinical and Genetic Findings in a Chinese Cohort of Dentatorubral–Pallidoluysian Atrophy Patients
3个月前
已完结
Determination of 21 amino acids in grass carp, clam and shrimp by enzymatic hydrolysis coupled with high-performance liquid chromatography and tandem mass spectrometry
3个月前
已完结
Prognostic impact ofDDX41germline mutations in intensively treated acute myeloid leukemia patients: an ALFA-FILO study
4个月前
已完结
Multiple nucleotide variants in genetic diagnosis: implications from 11,467 cases of hearing loss
4个月前
已完结
Large-scale genome-wide association analyses identify novel genetic loci and mechanisms in hypertrophic cardiomyopathy
7个月前
已完结
Diagnostic criteria and contributors to Gilbert’s syndrome
9个月前
已完结
Diagnostic criteria and contributors to Gilbert's syndrome
9个月前
已关闭
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