Results 251 to 260 of about 93,691 (297)
Some of the next articles are maybe not open access.
Complex chromosomal rearrangement and multiple spontaneous abortions
Human Genetics, 1986We report on a woman with a balanced complex chromosomal rearrangement (CCR) involving chromosomes 7, 10, and 21. She is the third individual with an apparently de novo CCR to be ascertained by repeated fetal wastage. Both familial and de novo CCRs are associated with recurrent spontaneous abortions.
J L, Gorski +3 more
openaire +2 more sources
What Is a Complex Chromosome Rearrangement?
American Journal of Medical Genetics Part A, 2013No single definition of a complex chromosome rearrangement (CCR) can adequately cover the whole range of possible structural rearrangements. There are highly complex CCRs with multiple breaks that involve three, four or more chromosomes, but there are also CCRs that involve just two chromosomes or even a single chromosome.
openaire +2 more sources
Delineation of complex chromosomal rearrangements: evidence for increased complexity
Human Genetics, 2004There is an assumption of parsimony with regard to the number of chromosomes involved in rearrangements and to the number of breaks within those chromosomes. Highly complex chromosome rearrangements are thought to be relatively rare, with the risk for phenotypic abnormalities increasing as the number of chromosomes and chromosomal breaks involved in ...
Caroline, Astbury +7 more
openaire +2 more sources
Unstable transmission of a familial complex chromosome rearrangement
American Journal of Medical Genetics Part A, 2012AbstractComplex chromosome rearrangements (CCRs) are rare genomic structural aberrations involving three or more breakpoints on two or more chromosomes. About one‐third of all CCRs are familial. Transmittance of such a CCR results either in genomic imbalance due to abnormal segregation at meiosis I or is stably passed on to the next generation. Here we
Ellen, van Binsbergen +3 more
openaire +2 more sources
Complex chromosome rearrangements in an extraabdominal desmoid tumor
Cancer Genetics and Cytogenetics, 1988Cytogenetic studies of an extraabdominal desmoid tumor revealed karyotypic abnormalities in 20 of 50 analyzed metaphases, with no less than 13 clonal marker chromosomes, 11 of which could be at least partially identified. The hypodiploid stemline karyotype was interpreted as: 43-45,XX,-1,-1, + der(1)(?::1p36----1q21::?) + der(1)t(1;?)(p11;?), + der(1) (
I, Karlsson +5 more
openaire +2 more sources
A complex balanced chromosomal rearrangement in repeated abortions
Human Genetics, 1987A double balanced reciprocal translocation involving four chromosomes, t(1;19;6;14) (1p11; 19p11; 6q25; 14q21), was found in the phenotypically normal husband in a couple referred because of repeated abortions. Reciprocal translocations, t(6;14), had been transmitted by his mother, his father being apparently homozygous for a translocation comprising ...
A, Barros +5 more
openaire +2 more sources
Complex chromosomal rearrangements associated with congenital erythrophagocytotic histiocytosis
Clinical Genetics, 1998We describe a patient with a congenital malignant blood disorder and a constitutional de novo chromosomal rearrangement that includes four breakpoints. By conventional cytogenetic analysis an obviously reciprocal balanced translocation with the breakpoints 1p36 and 5q11.2 was diagnosed.
S, Edelhoff +5 more
openaire +2 more sources
Complex chromosome rearrangements in prenatal diagnosis
European journal of human genetics, 2004Complex chromosome rearrangements (CCR) are defined as reciprocal exchanges between three or more chromosomes. It has been observed that most CCR carriers are female. CCr are very rare, with the risk for phenotypic abnormalities increasing as the number of chromosomes and chromosomal breaks involved in the rearrangement increases. The normal phenotypes
Mužinić-Belinec, Dubravka +3 more
openaire +2 more sources
Complex chromosomal rearrangements.
Genetic counseling (Geneva, Switzerland), 2007Complex Chromosomal Rearrangements (CCRs) are constitutional structural rearrangements involving three or more chromosomes or having more than two breakpoints. CCRs preferentially occur during spermatogenesis and are transmitted in families through oogenesis.
openaire +1 more source
FISH-microdissection (FISH-MD) analysis of complex chromosome rearrangements
Cytogenetic and Genome Research, 2000We combined the techniques of fluorescence in situ hybridization (FISH) and chromosomal microdissection in one experiment (FISH-MD). This novel method permits rapid identification of the composition, origin, and breakpoints of rearranged chromosomes. Rearranged chromosomes are first identified by multicolor-FISH, then the fluorophore-labeled derivative
J, Weimer, M, Kiechle, N, Arnold
openaire +2 more sources

