We report a 16-year-old girl who presented with short stature and amenorrhea. Initially the cytogenetic analysis showed the presence of a mosaic non-Robertsonian dicentric chromosome involving chromosomes 14 and 19. Subsequent molecular cytogenetic analysis by fluorescence in situ hybridization (FISH) using whole chromosome paints, centromeric probes, as well as gene specific probes confirmed the dicentric nature of the derivative chromosome and indicated that the rearrangement involved the short arms of both of these chromosomes. Furthermore, we also determined that the chromosome 19p13.3 breakpoint occurred within the terminal 1 Mb region. This is the first report of a mosaic non-Robertsonian dicentric chromosome involving chromosomes 14 ...
International audienceWe describe a female infant with severe abnormal phenotype with a de novo part...
CONTEXT: Robertsonian translocations (RT) are among the most common balanced structural rearrangemen...
Small supernumerary marker chromosomes (sSMCs) are structurally abnormal extra chromosomes that cann...
The molecular cytogenetic characterization and clinical description of 15 children with marker chr...
We report a 21-week gestation fetus terminated because of multiple congenital abnormalities seen on ...
The rearrangement of chromosome 14 is a rare cytogenetic finding. Changes in the number or structure...
We report on the characterization of a de novo, apparently balanced translocation t(X;15)(p11.3;q26)...
AbstractObjectiveTo present molecular cytogenetic characterization of an inverted duplication of pro...
Complex chromosome rearrangements (CCRs), which are rather rare in the whole population, may be asso...
We report on the cytogenetic, fluorescence in situ hybridization (FISH), and molecular results obtai...
International audienceChromoanagenesis represents an extreme form of genomic rearrangements involvin...
The balanced non-Robertsonian translocation (ROB) associated with acrocentric chromosomes is an unus...
A female infant with multiple malforma-tions and mental retardation was noted to have a rare de novo...
textabstractBackground. Complex chromosomal rearrangements (CCR) are rare cytogenetic findings that ...
We report a 20-year-old female with features evocative of Turner syndrome (short stature, broad trun...
International audienceWe describe a female infant with severe abnormal phenotype with a de novo part...
CONTEXT: Robertsonian translocations (RT) are among the most common balanced structural rearrangemen...
Small supernumerary marker chromosomes (sSMCs) are structurally abnormal extra chromosomes that cann...
The molecular cytogenetic characterization and clinical description of 15 children with marker chr...
We report a 21-week gestation fetus terminated because of multiple congenital abnormalities seen on ...
The rearrangement of chromosome 14 is a rare cytogenetic finding. Changes in the number or structure...
We report on the characterization of a de novo, apparently balanced translocation t(X;15)(p11.3;q26)...
AbstractObjectiveTo present molecular cytogenetic characterization of an inverted duplication of pro...
Complex chromosome rearrangements (CCRs), which are rather rare in the whole population, may be asso...
We report on the cytogenetic, fluorescence in situ hybridization (FISH), and molecular results obtai...
International audienceChromoanagenesis represents an extreme form of genomic rearrangements involvin...
The balanced non-Robertsonian translocation (ROB) associated with acrocentric chromosomes is an unus...
A female infant with multiple malforma-tions and mental retardation was noted to have a rare de novo...
textabstractBackground. Complex chromosomal rearrangements (CCR) are rare cytogenetic findings that ...
We report a 20-year-old female with features evocative of Turner syndrome (short stature, broad trun...
International audienceWe describe a female infant with severe abnormal phenotype with a de novo part...
CONTEXT: Robertsonian translocations (RT) are among the most common balanced structural rearrangemen...
Small supernumerary marker chromosomes (sSMCs) are structurally abnormal extra chromosomes that cann...