Results 281 to 290 of about 105,723 (318)
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Phenotypic effects of inherited balanced translocation
American Journal of Medical Genetics, 1982AbstractWe report two cases of inherited balanced translocation with severe CNS abnormalities and a number of other physical findings. In both cases a multiple congenital anomalies/mental retardation (MCA/MR) syndrome was supected However, in one case, parturitional and neonatal complications probably resulted in brain damage; in the other, prenatal ...
Zhao Ying +5 more
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Constitutional Balanced Translocations in Alveolar Rhabdomyosarcoma
Cancer Genetics and Cytogenetics, 1998Chromosomal analysis of tumor tissue from two children with alveolar rhabdomyosarcoma revealed t(1;5)(q32;q31) and t(1;22)(q21;q11.2) in all metaphases examined, respectively. Peripheral blood lymphocytes carried the same cytogenetic abnormality as that of the tumor cells in both patients.
S, Savaşan +10 more
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Balanced reciprocal translocation mosaicism: How frequent?
American Journal of Medical Genetics, 1995AbstractWe describe 2 cases of balanced reciprocal translocation (BRT) mosaicism. The frequency of this aberration in the population referred to our laboratory was determined and compared to those frequencies reported in the literature by other clinical cytogenetics laboratories.
K E, Opheim +3 more
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Two cases of C-group balanced translocations
Humangenetik, 1975The present study describes 2 cases of a balanced reciprocal translocation in the C-group of autosomes. Familial translocation 46,XX,t(6;7) was found both in a woman cytogenetically examined because of a developmental anomaly of the internal genitals (uterus bicornis subseptus) and in her healthy mother.
K, Michalová, J, Málková, R, Chrz
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Semen Analysis in Subfertile Balanced-Translocation Carriers
Fertility and Sterility, 1980The spermograms of 19 subfertile translocation carriers were analyzed. Most of these men had moderate oligo-/astheno-/teratospermia. The results were widely spread, and some reached normal values, suggesting that autosomal rearrangement of the karyotype does not lead to severe oligospermia or azoospermia as do sex chromosome aberrations.
D, Marmor +7 more
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Human Genetics, 1997
We report an unusual case of a balanced reciprocal translocation with a recombinant chromosome which has arisen from a familial balanced complex translocation. Fluorescence in situ hybridization studies were essential for the identification of the breakpoints.
K, Madan, A W, Nieuwint, Y, van Bever
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We report an unusual case of a balanced reciprocal translocation with a recombinant chromosome which has arisen from a familial balanced complex translocation. Fluorescence in situ hybridization studies were essential for the identification of the breakpoints.
K, Madan, A W, Nieuwint, Y, van Bever
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Azoospermic Male with a Balanced Y-Autosome Translocation
Urologia Internationalis, 1989Structural chromosomal aberrations, such as translocations or inversions, may cause spermatogenic failure. We report a rare chromosomal anomaly 46,X,t(Y;3)(q12;p21) in an azoospermic male with normal phenotype. Twenty-two cases of a balanced Y-autosome translocation have been reported in the literature and the majority of them have been detected among ...
T, Matsuda +4 more
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Balanced translocation in fetal wastage.
Obstetrics and gynecology, 1975A balanced reciprocal translocation involving the long arms of a No. 4 and a No. 11 chromosome, t(4;11) (q25;q13), was found in a mother who had one spontaneous first trimester abortion and 2 abnormal infants, as well as in her 2 phenotypically normal children.
H J, Kim +3 more
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Three cases of mosaicism for balanced reciprocal translocations
American Journal of Medical Genetics, 1998Mosaicism for a balanced reciprocal translocation (BRTM) is rare. As far as we know only 26 cases of BRTM, demonstrated in lymphocyte cultures, have been described, five of which had an abnormal phenotype. Prenatally three confirmed cases with a normal phenotypic outcome have been described.
Leegte, B +6 more
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An azoospermic male with presumably balanced reciprocal translocation
Clinical Genetics, 1983This report describes a physically normal man carrying a presumably balanced translocation between chromosomes 2 and 13. His karyotype was 46, XY, t(2;13)(q37;q15). The man was azoospermic. Testicular histology showed an arrest in spermatogenesis at the spermatocyte stage.
E, Lyberatou-Moraitou +3 more
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