Pages that link to "Q24557421"
Jump to navigation
Jump to search
The following pages link to Gene conversion and evolution of Xq28 duplicons involved in recurring inversions causing severe hemophilia A (Q24557421):
Displayed 16 items.
- A recurrent inversion on the eutherian X chromosome (Q28756249) (← links)
- Endothelial cell processing and alternatively spliced transcripts of factor VIII: potential implications for coagulation cascades and pulmonary hypertension (Q33533332) (← links)
- A W-linked palindrome and gene conversion in New World sparrows and blackbirds (Q34070337) (← links)
- Evidence for widespread reticulate evolution within human duplicons (Q34106726) (← links)
- Recombination dynamics of a human Y-chromosomal palindrome: rapid GC-biased gene conversion, multi-kilobase conversion tracts, and rare inversions (Q34363329) (← links)
- Nonrecurrent MECP2 duplications mediated by genomic architecture-driven DNA breaks and break-induced replication repair. (Q34767093) (← links)
- How homologous recombination generates a mutable genome (Q36273640) (← links)
- Sexy gene conversions: locating gene conversions on the X-chromosome (Q37298551) (← links)
- Gene conversion in angiosperm genomes with an emphasis on genes duplicated by polyploidization (Q37585028) (← links)
- Y chromosome palindromes and gene conversion (Q39183110) (← links)
- Characterization of equine and other vertebrate TLR3, TLR7, and TLR8 genes (Q45817958) (← links)
- Int22h-related inversions causing hemophilia A: a novel insight into their origin and a new more discriminant PCR test for their detection. (Q45855830) (← links)
- Novel characterization of a breakpoint in F8: an individualized approach to gene analysis when PCR and MLPA results contradict. (Q45872407) (← links)
- Computational and molecular approaches for predicting unreported causal missense mutations in Belgian patients with haemophilia A. (Q45872903) (← links)
- Polymorphism and hemophilia A causing inversions in distal Xq28: a complex picture (Q45887888) (← links)
- Opposite Expression Patterns of Spry3 and p75NTR in Cerebellar Vermis Suggest a Male-Specific Mechanism of Autism Pathogenesis (Q91637858) (← links)