Lv3
290 积分 2022-07-21 加入
Genetic mutation analysis of 22 patients with congenital absence of vas deferens: a single-center study
2个月前
已完结
Identification of novel mutations in HFE, HFE2, TfR2, and SLC40A1 genes in Chinese patients affected by hereditary hemochromatosis
3个月前
已完结
Rapid detection of α‐thalassaemia deletions and α‐globin gene triplication by multiplex polymerase chain reactions
6个月前
已完结
Rapid detection of the common mediterranean α-globin deletions/rearrangements using PCR
6个月前
已完结
Newborn Screening for SMA – Can a Wait-and-See Strategy be Responsibly Justified in Patients With Four SMN2 Copies?
6个月前
已完结
Analysis of the coding regions of VEGFR3 and VEGFC in Milroy disease and other primary lymphoedemas
7个月前
已完结
Genotype/phenotype correlation in 325 individuals referred for a diagnosis of tuberous sclerosis complex in the United States
10个月前
已完结
Mutational spectrum of the TSC1 gene in a cohort of 225 tuberous sclerosis complex patients: no evidence for genotype-phenotype correlation
10个月前
已完结
Disorders of Hemoglobin: Genetics, Pathophysiology, and Clinical Management
10个月前
已完结
Investigation of the mechanism of copy number variations involving the α-globin gene cluster on chromosome 16: two case reports and literature review
10个月前
已完结
Prevention of Hepatitis B Virus Infection in the United States: Recommendations of the Advisory Committee on Immunization Practices
Lipid nanoparticle-mediated lymph node–targeting delivery of mRNA cancer vaccine elicits robust CD8 + T cell response
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