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Meiotic and sperm chromosome studies in a reciprocal translocation t(1;2)(q32;q36)

✍ Scribed by C. Templado; J. Navarro; R. Requena; J. Benet; F. Ballesta; J. Egozcue


Publisher
Springer
Year
1990
Tongue
English
Weight
339 KB
Volume
84
Category
Article
ISSN
0340-6717

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Sperm chromosome complements have been studied in a man heterozygous for a reciprocal translocation t(2;5)(p11;q15). Human sperm chromosomes were obtained after fertilization of zona-free hamster eggs. A total of 75 human sperm metaphases were analysed. On the complements studied, 59 (78.6%) resulte

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## Abstract Cytogenetic studies of a rhabdomyosarcoma of mixed embryonal and alveolar histology in an II ‐month‐old male revealed a single structural abnormality, t(1;13)(p36;q14). This abnormality may define a subset of patients with a variant of the t(2;13)(q35;q14) translocation frequently seen