Several studies have shown the importance of segmental deletions/duplications in the field of chromosome pathologies. Non allelic homologous recombination, NAHR, between chromosomes or sister chromatids, mediated by segmental duplications, is the foundation of frequent mechanisms for structural chromosome mutations such as micro-deletions, micro-duplications, translocations, inversions, and marker chromosomes. We analyzed three distinct genomic regions (22q11.2, 17p11.2, 16p11.2) and we discussed how the same chromosome region can be affected by deletion or by reciprocal duplication, respectively responsible for a syndrome or for a reciprocal counter-syndrome, with different phenotypic manifestation
Apparently balanced chromosome rearrangements (ABCRs), mainly reciprocal translocations and inversio...
The chromosome 22q11.2 region has long been implicated in genomic diseases. Some genomic regions exh...
Using array comparative genome hybridisation (CGH) 41 de novo reciprocal translocations and 18 de no...
Several studies have shown the importance of segmental deletions/duplications in the field of chromo...
Nonallelic homologous recombination (NAHR) mediated by LCRs (low-copy repeats) produces chromosomal ...
Insights into the origins of structural variation and the mutational mechanisms underlying genomic d...
Nearly all recurrent microdeletion/duplication syndromes described to date are characterized by the ...
Background: The 22q11.2 deletion syndrome is the most frequent genomic disorder with an estimated f...
We have explored the National Center for Biotechnology Information (NCBI) single nucleotide polymorp...
Abstract Recent studies have identified a small number of genomic rearrangements that occur frequent...
Genomic disorders constitute a class of diseases that are associated with DNA rearrangements resulti...
A number of common contiguous gene syndromes have been shown to result from nonallelic homologous re...
The human genome contains numerous blocks of highly homologous duplicated sequence. This higher-orde...
Inborn chromosome abnormalities are a frequent cause of mental retardation and birth defects. Apart...
Recent studies have identified a small number of genomic rearrangements that occur frequently in the...
Apparently balanced chromosome rearrangements (ABCRs), mainly reciprocal translocations and inversio...
The chromosome 22q11.2 region has long been implicated in genomic diseases. Some genomic regions exh...
Using array comparative genome hybridisation (CGH) 41 de novo reciprocal translocations and 18 de no...
Several studies have shown the importance of segmental deletions/duplications in the field of chromo...
Nonallelic homologous recombination (NAHR) mediated by LCRs (low-copy repeats) produces chromosomal ...
Insights into the origins of structural variation and the mutational mechanisms underlying genomic d...
Nearly all recurrent microdeletion/duplication syndromes described to date are characterized by the ...
Background: The 22q11.2 deletion syndrome is the most frequent genomic disorder with an estimated f...
We have explored the National Center for Biotechnology Information (NCBI) single nucleotide polymorp...
Abstract Recent studies have identified a small number of genomic rearrangements that occur frequent...
Genomic disorders constitute a class of diseases that are associated with DNA rearrangements resulti...
A number of common contiguous gene syndromes have been shown to result from nonallelic homologous re...
The human genome contains numerous blocks of highly homologous duplicated sequence. This higher-orde...
Inborn chromosome abnormalities are a frequent cause of mental retardation and birth defects. Apart...
Recent studies have identified a small number of genomic rearrangements that occur frequently in the...
Apparently balanced chromosome rearrangements (ABCRs), mainly reciprocal translocations and inversio...
The chromosome 22q11.2 region has long been implicated in genomic diseases. Some genomic regions exh...
Using array comparative genome hybridisation (CGH) 41 de novo reciprocal translocations and 18 de no...