Associated Papers
Noninvasive fetal genotyping of single nucleotide variants and linkage analysis for prenatal diagnosis of monogenic disorders.
Wu W et al.
Human Genomics, 2022
35897115 (PubMed )
Supplement: 40246_2022_400_MOESM1_ESM.xlsx › Primer_sequences
Genomic alterations in the F8 gene correlating with severe hemophilia A in Egyptian patients.
Mosaad RM et al.
Molecular Genetics & Genomic Medicine, 2021
Select a paper to view details