A 13;13 tandem chromosome translocation in a subject with congenital anomalies. Repository identification No. GM-2018.
作者信息
Kohn G, Cohen M M, Aronson M M, Greene A E, Coriell L L
出版信息
Cytogenet Cell Genet. 1979;24(1):72. doi: 10.1159/000131359.
PMID:456042
Abstract
摘要
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1
A 13;13 tandem chromosome translocation in a subject with congenital anomalies. Repository identification No. GM-2018.一名患有先天性异常的受试者中出现13;13串联染色体易位。储存库识别号：GM - 2018。
Cytogenet Cell Genet. 1979;24(1):72. doi: 10.1159/000131359.
2
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A homologous tandem translocation [45,XX,-13,-13,+t(13;13) (q12;q34)].同源串联易位[45,XX,-13,-13,+t(13;13)(q12;q34)]
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6
Chromosome 6/15 translocation with multiple congenital anomalies.伴有多种先天性异常的6号/15号染色体易位
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7
Duplication of a segment of chromosome 3 in a subject with multiple congenital anomalies and a 47,XYY father, inversion of chromosomes 3 and 9 in the mother, and inversion of chromosome 9 in a brother. Repository identification Nos. GM-1253, GM-1252, and GM-1251.一名患有多种先天性异常的患者存在3号染色体片段重复，其父亲为47,XYY，母亲存在3号和9号染色体倒位，其兄弟存在9号染色体倒位。储存库识别编号：GM - 1253、GM - 1252和GM - 1251。
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8
A (2;4) translocation, unbalanced, 46 chromosomes. Repository identification No. GM-501.一种不平衡的（2；4）易位，46条染色体。保藏编号GM - 501。
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Partial trisomy for the distal long arm of chromosome 13, 46,,XY. Repository identification No. GM-1663.13号染色体长臂远端部分三体，核型46，XY。库识别号GM - 1663。
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A culture with a derivative chromosome 10 from a paternal (10;16) translocation. Repository identification no. GM-1396.一种具有源自父系（10；16）易位的衍生10号染色体的培养物。保藏编号GM-1396。
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