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Physical and mental defect of chromosomal origin in four individuals of the same family. Trisomy for the short arm of 9.

作者信息

Blank C E, Colver D C, Potter A M, McHugh J, Lorber J

出版信息

Clin Genet. 1975 Apr;7(4):261-73. doi: 10.1111/j.1399-0004.1975.tb00328.x.

DOI:10.1111/j.1399-0004.1975.tb00328.x
PMID:1126048
Abstract

A family with the reciprocal translocation t(9;22)(q13;q11) segregating in genetically balanced and unbalanced form is identified. The clinical features of four members with trisomy for the short arm of 9, and the proximal part of the long arm of 9, are described in detail. Features in common are summarized and compared with developmental abnormality observed in other examples of trisomy for the short arm of 9. An attempt is made to delineate further the clinical features commonly seen in trisomy for the short arm of 9.

摘要

相似文献

1
Physical and mental defect of chromosomal origin in four individuals of the same family. Trisomy for the short arm of 9.
Clin Genet. 1975 Apr;7(4):261-73. doi: 10.1111/j.1399-0004.1975.tb00328.x.
2
Partial trisomy of chromosome no. 1 in two adult brothers due to maternal translocation (1q--;6p+).由于母亲的染色体易位(1q--;6p+),两名成年兄弟出现1号染色体部分三体。
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7
Partial trisomy 7p associated with familial 7p;22q translocation.与家族性7号染色体短臂;22号染色体长臂易位相关的7号染色体短臂部分三体性
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Partial trisomy of 13(pter to q12) due to 47,XY, + der(13),t(13;22)(q12;q13)mat.因47,XY, + der(13),t(13;22)(q12;q13)mat导致的13号染色体部分三体(pter至q12)
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引用本文的文献

1
A Systematic Review of Reproductive Counseling in Cases of Parental Constitutional Reciprocal Translocation (9;22) Mimicking BCR-ABL1.模仿BCR-ABL1的父母染色体相互易位(9;22)病例中生殖咨询的系统评价
Front Genet. 2022 Aug 4;13:921910. doi: 10.3389/fgene.2022.921910. eCollection 2022.
2
Viability thresholds for partial trisomies and monosomies. A study of 1,159 viable unbalanced reciprocal translocations.部分三体和单体的存活阈值。对1159例存活的不平衡相互易位的研究。
Hum Genet. 1994 Feb;93(2):188-94. doi: 10.1007/BF00210608.
3
Reciprocal translocations: a way to predict the mode of imbalanced segregation by pachytene-diagram drawing.
相互易位:一种通过粗线期图绘制预测不平衡分离模式的方法。
Hum Genet. 1980;55(2):209-22. doi: 10.1007/BF00291769.
4
A deletion in chromosome 22 can cause DiGeorge syndrome.22号染色体的缺失会导致迪乔治综合征。
Hum Genet. 1981;57(3):253-6. doi: 10.1007/BF00278938.
5
Adjacent 2 meiotic disjunction. report of a case resulting from a familial 13q;15q balanced reciprocal translocation and review of the literature.相邻2减数分裂分离。1例由家族性13号染色体长臂;15号染色体长臂平衡易位导致的病例报告及文献复习
Hum Genet. 1981;58(4):377-86. doi: 10.1007/BF00282819.
6
Trisomy 9p due to paternal translocation, t(9;13) (q13;q12).由于父源易位t(9;13)(q13;q12)导致的9号染色体短臂三体。
Humangenetik. 1975 Dec 23;30(4):307-16. doi: 10.1007/BF00275143.
7
Possible intrachromosomal duplication in a case of trisomy 9p.9号染色体短臂三体综合征一例中可能存在的染色体内重复。
Hum Genet. 1976 Oct 28;34(2):217-21. doi: 10.1007/BF00278892.
8
Structural variability of human chromosome 9 in relation to its evolution.人类9号染色体的结构变异及其进化关系
Hum Genet. 1976 Mar 12;31(3):247-62. doi: 10.1007/BF00270855.
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Complex translocation t(9;21)(9;22)(q12p13)(q12q11) in the family of a child with 9p trisomy syndrome.一名患有9p三体综合征儿童的家族中出现复杂易位t(9;21)(9;22)(q12p13)(q12q11) 。
Hum Genet. 1976 Jul 7;33(1):73-6. doi: 10.1007/BF00447289.
10
Familial trisomy 9p and spinal muscular atrophy: clinical, cytogenetic and embryological findings.家族性9号染色体短臂三体与脊髓性肌萎缩症:临床、细胞遗传学及胚胎学研究结果
Eur J Pediatr. 1977 Aug 23;126(1-2):13-27. doi: 10.1007/BF00443119.