Results 151 to 160 of about 3,485 (190)
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2011
Abstract THE AMERICAN INSECT CYTOGENETICIST W. R. B. Robertson first described translocations of chromosomes resulting from the fusion of two acrocentrics in his study of insect speciation in 1916, and this type of translocation is named Robertsonian (abbreviation rob) in his honor.
R. J. McKinlay Gardner +2 more
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Abstract THE AMERICAN INSECT CYTOGENETICIST W. R. B. Robertson first described translocations of chromosomes resulting from the fusion of two acrocentrics in his study of insect speciation in 1916, and this type of translocation is named Robertsonian (abbreviation rob) in his honor.
R. J. McKinlay Gardner +2 more
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Severe Hypospadias Associated with Robertsonian Translocation
Urologia Internationalis, 2005In this study, we report a 3-year-old boy with severe scrotal hypospadias with Robertsonian translocation [45,XY,t(13q;14q)]. The patient was born at term with a low birth weight and hypospadias. There was no endocrinological abnormality. His father also has a balanced 13–14 Robertsonian translocation. Two-stage hypospadias repair was carried out.
Saglam, HALİL +4 more
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Robertsonian translocation in a Zebu bull
Theriogenology, 1985Karyotypes were prepared for ten Rahaji bulls using cultured peripheral blood lymphocytes. C-banded metaphases were prepared to identify the sex chromosomes and possible translocations. Out of the ten bulls, studied one bull had a 2n number of 59 chromosomes and carried a Robertsonian translocation.
N, Pathiraja +2 more
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Robertsonian translocation in Sykia Chalkidiki cattle
Theriogenology, 1992This is the first report on the Robertsonian 1/29 translocation in the Sykia Chalkidiki cattle breed. The characteristics of this endangered breed are described, and the possibilities of rescuing and exploiting the breed in a zootechnical sense are examined.
E, Vainas, N, Belibasakis, C, Boscos
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Homologous Robertsonian translocation (21q21q) and abortions
Human Genetics, 1990Instances of balanced Robertsonian translocations between the homologues of chromosome 21 were observed in two couples with a history of repeated abortions. The male partner of one couple and the female partner of another couple exhibited this anomaly. The translocation (21q21q) was found to be transmitted to their live children with Down's syndrome.
T, Sudha, P M, Gopinath
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Translocation chromosome karyotypes of the Robertsonian translocation carriers' embryos
Fertility and Sterility, 2010To explore the translocation karyotypes of the Robertsonian translocation (RT) carriers' embryos in their preimplantation genetic diagnosis (PGD) cycles.Retrospective.University-affiliated IVF center.A total of 35 RT carrier couples underwent 39 blastomere PGD cycles from August 2005 to June 2008.The PGD analysis of embryos.Meiotic segregation patterns
Huang, Jin +4 more
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2018
Abstract Robertsonian translocations are among the most common balanced structural rearrangements seen in the general population, with a frequency in newborn surveys of about 1 in 1,000. Robertsonian translocations have their own peculiar characteristics and need to be considered separately.
David J. Amor, R. J. McKinlay Gardner
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Abstract Robertsonian translocations are among the most common balanced structural rearrangements seen in the general population, with a frequency in newborn surveys of about 1 in 1,000. Robertsonian translocations have their own peculiar characteristics and need to be considered separately.
David J. Amor, R. J. McKinlay Gardner
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Glomemlonephritis Associated with Robertsonian Translocation t(13;14)
Nephron, 1992We report the first case of glomerulonephritis associated with Robertsonian translocation t(13;14) in a 18-year-old female. The renal biopsy revealed mesangial proliferative glomerulonephritis with mesangial IgG and C3 deposits. The patient also has congenital absence of ovaries and an underdeveloped uterus. Our report suggests that renal abnormalities
P K, Li, F M, Lai, J C, Lee, K N, Lai
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Robertsonian translocations in Paget's disease of bone
Journal of Orthopaedic Research, 1997AbstractThe karyotypes of 14 patients with Paget's disease of bone were studied. The patients were recruited from our bone metabolism clinic where they received specific therapy for their skeletal disease. Eight of the 14 patients had chromosomal translocations localized to the D and G groups.
B G, Mills, J, Oizumi, E, Kudo, R, Rude
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