The small size of the mitochondrial (mt) genome and its presence in many copies per cell make it useful for human DNA typing when only small amounts of material are available or when the material is badly degraded [1]. Despite its small size, and the fact that it is normally transmitted only maternally and without recombination, substantial DNA sequence polymorphism has accumulated in the mt genome, especially in two segments of the control region: HVI and HVII. The mtDNA sequence recovered from an item of evidence can thus be used to exclude many individuals as potential sources of that evidence. Conversely, if an evidence sequence matches a known reference sequence, the fre-quency of unrelated individuals who match the evidence sequence c...
The principal limitation in forensic mitochondrial DNA (mtDNA) testing is the low power of discrimin...
Heteroplasmy, the existence of multiple mtDNA types within an individual, has been previously detect...
A majority of mitochondrial DNA (mtDNA) mutations reported to be implicated in diseases are heteropl...
The presence of hundreds of copies of mitochondrial (mt) DNA in each human cell poses a challenge fo...
Sequence analysis of human mitochondrial DNA (mtDNA) is an effective and reliable tool for the genet...
Recent reports have questioned the accepted dogma that mammalian mitochondrial DNA (mtDNA) is strict...
Approximately 2.4% of the human mitochondrial DNA (mtDNA) genome exhibits common homoplasmic genetic...
Mitochondrial DNA (mtDNA) has been the marker of choice since the advent of phylogeography, and for ...
DNA sequencing identifies common and rare genetic variants for association studies, but studies typi...
The standard paradigm postulates that the human mitochondrial genome (mtDNA) is strictly maternally ...
Sanger sequencing of the mitochondrial DNA (mtDNA) control region was previously the only method ava...
The standard paradigm postulates that the human mitochondrial genome (mtDNA) is strictly maternally ...
Mitochondrial DNA (mtDNA) analysis is a potent tool in human population/evolution studies and, more ...
Analyses of hypervariable segments of mitochondrial DNA (mtDNA) are currently being used for forensi...
AbstractLong an important and useful tool in forensic genetic investigations, mitochondrial DNA (mtD...
The principal limitation in forensic mitochondrial DNA (mtDNA) testing is the low power of discrimin...
Heteroplasmy, the existence of multiple mtDNA types within an individual, has been previously detect...
A majority of mitochondrial DNA (mtDNA) mutations reported to be implicated in diseases are heteropl...
The presence of hundreds of copies of mitochondrial (mt) DNA in each human cell poses a challenge fo...
Sequence analysis of human mitochondrial DNA (mtDNA) is an effective and reliable tool for the genet...
Recent reports have questioned the accepted dogma that mammalian mitochondrial DNA (mtDNA) is strict...
Approximately 2.4% of the human mitochondrial DNA (mtDNA) genome exhibits common homoplasmic genetic...
Mitochondrial DNA (mtDNA) has been the marker of choice since the advent of phylogeography, and for ...
DNA sequencing identifies common and rare genetic variants for association studies, but studies typi...
The standard paradigm postulates that the human mitochondrial genome (mtDNA) is strictly maternally ...
Sanger sequencing of the mitochondrial DNA (mtDNA) control region was previously the only method ava...
The standard paradigm postulates that the human mitochondrial genome (mtDNA) is strictly maternally ...
Mitochondrial DNA (mtDNA) analysis is a potent tool in human population/evolution studies and, more ...
Analyses of hypervariable segments of mitochondrial DNA (mtDNA) are currently being used for forensi...
AbstractLong an important and useful tool in forensic genetic investigations, mitochondrial DNA (mtD...
The principal limitation in forensic mitochondrial DNA (mtDNA) testing is the low power of discrimin...
Heteroplasmy, the existence of multiple mtDNA types within an individual, has been previously detect...
A majority of mitochondrial DNA (mtDNA) mutations reported to be implicated in diseases are heteropl...