Pages that link to "Q69809070"
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The following pages link to A sex chromosome rearrangement in a human XX male caused by Alu-Alu recombination (Q69809070):
Displayed 50 items.
- Human signal recognition particle (SRP) Alu-associated protein also binds Alu interspersed repeat sequence RNAs. Characterization of human SRP9 (Q24315915) (← links)
- Structural organization of glycophorin A and B genes: glycophorin B gene evolved by homologous recombination at Alu repeat sequences (Q24339514) (← links)
- Unique sequence organization and erythroid cell-specific nuclear factor-binding of mammalian theta 1 globin promoters (Q24635562) (← links)
- Alu mobile elements: from junk DNA to genomic gems (Q28661722) (← links)
- Ubiquitous mammalian-wide interspersed repeats (MIRs) are molecular fossils from the mesozoic era (Q28776504) (← links)
- DNA methylation in health and disease (Q30659938) (← links)
- DNA methylation, methyltransferases, and cancer (Q30993657) (← links)
- Newly arisen DNA repeats in primate phylogeny (Q31160570) (← links)
- Construction of a human chromosome 4 YAC pool and analysis of artificial chromosome stability (Q33227826) (← links)
- X/Y translocations resulting from recombination between homologous sequences on Xp and Yq. (Q33412558) (← links)
- Long-range restriction map of the terminal part of the short arm of the human X chromosome (Q33579172) (← links)
- Asymmetry in chromosome pairing: a major factor in de novo mutation and the production of genetic disease in man (Q33593235) (← links)
- Short stature in a girl with a terminal Xp deletion distal to DXYS15: localisation of a growth gene(s) in the pseudoautosomal region (Q33594192) (← links)
- Chromosomal localisation of a pseudoautosomal growth gene(s) (Q33594421) (← links)
- Exchange of terminal portions of X- and Y-chromosomal short arms in human XY females (Q33847127) (← links)
- Localization of preferential sites of rearrangement within the BCR gene in Philadelphia chromosome-positive acute lymphoblastic leukemia (Q33867942) (← links)
- An interspersed repeated sequence specific for human subtelomeric regions (Q33917989) (← links)
- Allelic and ectopic recombination between Ty elements in yeast. (Q33954284) (← links)
- Targeted breakage of a human chromosome mediated by cloned human telomeric DNA (Q34231869) (← links)
- Junctions between genes in the haptoglobin gene cluster of primates (Q34295830) (← links)
- DNA methylation affects meiotic trans-sensing, not meiotic silencing, in Neurospora (Q34569317) (← links)
- Is zinc-finger Y the sex-determining gene? (Q35197427) (← links)
- A high frequency of length polymorphisms in repeated sequences adjacent to Alu sequences (Q35197825) (← links)
- Suppression of crossing-over by DNA methylation in Ascobolus (Q35198972) (← links)
- The preference for GT-rich DNA by the yeast Rad51 protein defines a set of universal pairing sequences (Q35199876) (← links)
- Partial gene duplication as a cause of human disease (Q35221528) (← links)
- Characterization of six partial deletions in the low-density-lipoprotein (LDL) receptor gene causing familial hypercholesterolemia (FH) (Q35246204) (← links)
- Molecular cytogenetic analysis of telomere rearrangements (Q35540299) (← links)
- Unbalanced translocations arise from diverse mutational mechanisms including chromothripsis (Q35793506) (← links)
- A recurrent translocation is mediated by homologous recombination between HERV-H elements (Q35799446) (← links)
- Physical mapping of the human pseudo-autosomal region; comparison with genetic linkage map. (Q36062906) (← links)
- A genetically determined insertion/deletion related polymorphism in human T cell receptor beta chain (TCRB) includes functional variable gene segments (Q36363844) (← links)
- Identification of a precursor genomic segment that provided a sequence unique to glycophorin B and E genes (Q36456810) (← links)
- Gene conversion as a secondary mechanism of short interspersed element (SINE) evolution (Q36566264) (← links)
- Cloning a balanced translocation associated with DiGeorge syndrome and identification of a disrupted candidate gene (Q36694090) (← links)
- Splice-mediated insertion of an Alu sequence inactivates ornithine delta-aminotransferase: a role for Alu elements in human mutation (Q37386470) (← links)
- Human somatic mutation assays as biomarkers of carcinogenesis (Q37528645) (← links)
- Complex recombination events at the hypermutable minisatellite CEB1 (D2S90). (Q37634399) (← links)
- A sterile male with 45,X0 and a Y;22 translocation (Q37775853) (← links)
- Isolation of an Alu repetitive DNA binding protein and effect of CpG methylation on binding to its recognition sequence (Q38338865) (← links)
- Human Structural Variation: Mechanisms of Chromosome Rearrangements (Q38553771) (← links)
- Requirements for ectopic homologous recombination in mammalian somatic cells (Q40020577) (← links)
- Identification of novel Runx1 (AML1) translocation partner genes SH3D19, YTHDf2, and ZNF687 in acute myeloid leukemia (Q40305071) (← links)
- One short well conserved region of Alu-sequences is involved in human gene rearrangements and has homology with prokaryotic chi. (Q40392697) (← links)
- The mammalian genome shaping activity of reverse transcriptase (Q40396339) (← links)
- Sequence conservation in Alu evolution. (Q40448415) (← links)
- Nucleotide sequence of both reciprocal translocation junction regions in a patient with Ph positive acute lymphoblastic leukaemia, with a breakpoint within the first intron of the BCR gene (Q40520345) (← links)
- Recombinational resolution in primate cells of two homologous human DNA segments with a gradient of sequence divergence (Q40557573) (← links)
- Recombinational biases in the rearranged C1-inhibitor genes of hereditary angioedema patients (Q40569057) (← links)
- Mechanisms of tandem duplication in the Duchenne muscular dystrophy gene include both homologous and nonhomologous intrachromosomal recombination (Q41082050) (← links)