Lv2
140 积分 2023-12-19 加入
Identification of rare heterozygous missense mutations in FANCA in esophageal atresia patients using next-generation sequencing
9天前
已关闭
Phenotypic and genotypic correlation evaluation of 148 pediatric patients with Fanconi anemia in a Chinese rare disease cohort
9天前
已完结
USH2A variants in Chinese patients with Usher syndrome type II and non-syndromic retinitis pigmentosa
17天前
已关闭
Clinical and genetic spectrum of children with congenital diarrhea and enteropathy in China
18天前
已完结
Inherited Genetic Susceptibility to Nonimmunosuppressed Epstein-Barr Virus-associated T/NK-cell Lymphoproliferative Diseases in Chinese Patients
26天前
已完结
Genomic alterations important for the prognosis in patients with follicular lymphoma treated in SWOG study S0016
1个月前
已完结
Genomic landscape of follicular lymphoma across a wide spectrum of clinical behaviors
1个月前
已完结
Comprehensive analysis of copy number and allele status identifies multiple chromosome defects underlying follicular lymphoma pathogenesis
1个月前
已完结
Genomic landscape of follicular lymphoma across a wide spectrum of clinical behaviors
2个月前
已完结
Sequential karyotyping in Burkitt lymphoma reveals a linear clonal evolution with increase in karyotype complexity and a high frequency of recurrent secondary aberrations
2个月前
已完结
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