患有10号染色体短臂三体综合征的兄妹：一种新综合征。 - Suppr

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Brother and sister with trisomy 10p: a new syndrome.

作者信息

Schleiermacher E, Schliebitz U, Steffens C

出版信息

Humangenetik. 1974;23(3):163-72. doi: 10.1007/BF00285102.

DOI:10.1007/BF00285102

PMID:4844639

Abstract

摘要

相似文献

Brother and sister with trisomy 10p: a new syndrome.患有10号染色体短臂三体综合征的兄妹：一种新综合征。

Humangenetik. 1974;23(3):163-72. doi: 10.1007/BF00285102.

Trisomy iop. A report of two cases due to a familial translocation rcp (10;21) (pII;pII).10号染色体三体。两例因家族性10号与21号染色体相互易位（10号染色体短臂与21号染色体短臂相互易位）导致的病例报告

Ann Genet. 1975 Mar;18(1):5-11.

Partial trisomy 11 in a child resulting from a complex maternal rearrangement of chromosomes 11, 12 and 13.一名儿童因母亲染色体11、12和13的复杂重排而导致11号染色体部分三体。

Humangenetik. 1974 Apr 24;22(1):59-65. doi: 10.1007/BF00338135.

Partial F trisomy associated with familial F-13 translocation detected and identified by parental chromosome studies.通过亲代染色体研究检测并鉴定出与家族性F-13易位相关的部分F三体。

J Pediatr. 1971 Apr;78(4):664-72. doi: 10.1016/s0022-3476(71)80471-7.

An (11;21) translocation in four generations with chromosome 11 abnormalities in the offspring. A clinical, cytogenetical, and gene marker study.一个连续四代出现（11；21）易位且子代存在11号染色体异常的家系。一项临床、细胞遗传学及基因标记研究。

Hum Hered. 1973;23(6):568-85. doi: 10.1159/000152624.

[Cp trisomy: a new syndrome].[18号染色体三体：一种新综合征]

Ann Genet. 1971 Sep;14(3):177-86.

Trisomy for the short arms of chromosome 9 in two generations, with balanced translocations t(15pplus;9qminus) in three generations.两代人中9号染色体短臂三体，三代人中存在平衡易位t(15加;9减) 。

J Pediatr. 1974 Jul;85(1):92-5. doi: 10.1016/s0022-3476(74)80296-9.

Partial trisomy 10p in two generations.两代人中的部分10号染色体短臂三体性

Hum Genet. 1978 Mar 17;41(2):235-41. doi: 10.1007/BF00273107.

New chromosomal syndromes.新的染色体综合征

Am J Dis Child. 1975 Apr;129(4):515-29. doi: 10.1001/archpedi.1975.02120410075021.

Partial trisomy 4q and partial monosomy 18q as a consequence of a paternal balanced translocation t(4qminus; 18qplus).由于父亲的平衡易位t(4q减;18q加)导致的4q部分三体和18q部分单体。

Humangenetik. 1974;25(3):227-33. doi: 10.1007/BF00281431.

引用本文的文献

Goyal-Naqvi Syndrome (Concurrent Trisomy 10p and Terminal 14q Deletion): A Review of the Literature.戈亚尔-纳克维综合征（10号染色体短臂三体与14号染色体长臂末端缺失并存）：文献综述

Cureus. 2021 Jul 26;13(7):e16652. doi: 10.7759/cureus.16652. eCollection 2021 Jul.

A Rare and Unusual Case of Trisomy 10p with Terminal 14q Deletion: A Multidisciplinary Approach.一例罕见的10号染色体短臂三体合并14号染色体长臂末端缺失病例：多学科诊疗方法

Cureus. 2021 Jun 5;13(6):e15459. doi: 10.7759/cureus.15459. eCollection 2021 Jun.

Neurophysiological findings in a newborn with chromosome 10 trisomy.一名患有10号染色体三体综合征新生儿的神经生理学检查结果

BMJ Case Rep. 2014 May 5;2014:bcr2013010222. doi: 10.1136/bcr-2013-010222.

Clinical findings associated with a de novo partial trisomy 10p11.22p15.3 and monosomy 7p22.3 detected by chromosomal microarray analysis.通过染色体微阵列分析检测到的与新发10p11.22p15.3部分三体和7p22.3单体相关的临床发现。

Case Rep Genet. 2011;2011:131768. doi: 10.1155/2011/131768. Epub 2011 Dec 8.

Duplication deficiency as the result of meiotic segregation of a maternal InV (10).由于母源10号染色体倒位（InV(10)）减数分裂分离导致的重复缺失

Hum Genet. 1981;57(1):71-4. doi: 10.1007/BF00271171.

Two chromosomal syndromes in the same family: monosomy and trisomy for part of the short arm of chromosome 10.同一家族中的两种染色体综合征：10号染色体短臂部分单体性和三体性。

Eur J Pediatr. 1982 Oct;139(2):153-7. doi: 10.1007/BF00441502.

Nonrandom distribution of exchange points in patients with structural rearrangements.结构重排患者交换点的非随机分布。

Am J Hum Genet. 1976 Jan;28(1):31-41.

Partial trisomy 10p.10号染色体短臂部分三体

Humangenetik. 1975 Sep 10;29(2):141-4. doi: 10.1007/BF00430351.

Del (10)p autosomal deletion syndrome: clinical, cytogenetic and gene marker studies.

Humangenetik. 1975;26(4):343-51. doi: 10.1007/BF00285386.

Risk for short arm 10 trisomy. A segregation analysis of eleven families with different translocations.短臂10三体的风险。对11个具有不同易位的家族进行的分离分析。

Hum Genet. 1977 Nov 2;39(1):7-13. doi: 10.1007/BF00273148.

本文引用的文献

[Dominant hereditary perodactylia in 4 generations of a family; a phenogenetic study].[一个家族四代人中的显性遗传性多指（趾）畸形；一项表型遗传学研究]

Z Mensch Vererb Konstitutionsl. 1954;32(4):277-307.

Presumed trisomy for the short arm of chromosome No. 9 not due to inherited translocation.推定9号染色体短臂三体性，非遗传性易位所致。

Humangenetik. 1971;12(3):175-81. doi: 10.1007/BF00702772.

[Partial trisonomy C9 in a case of balanced maternal B4-C9 translocation].[一例母亲B4-C9平衡易位病例中的9号染色体部分三体]

Z Kinderheilkd. 1971;109(4):293-9.

[4 cases of trisomy for the short arm of chromosome 9. Individualization of a new morbid entity].4例9号染色体短臂三体。一种新的病态实体的个体化研究

Ann Genet. 1970 Dec;13(4):217-32.

A familial translocation t(6q+;8q-) identified by fluorescence microscopy.通过荧光显微镜鉴定出的家族性易位t(6q+;8q-)

Humangenetik. 1973 Apr 16;18(2):189-92. doi: 10.1007/BF00291490.

C8 trisomy mosaicism syndrome.8号染色体三体嵌合综合征

Helv Paediatr Acta. 1972 Jul;27(3):281-98.

Partial trisomy of 7q resulting from a familial translocation.由家族性易位导致的7号染色体长臂部分三体。

Ann Genet. 1973 Mar;16(1):51-4.

[2 familial translocations occurring together in each of 2 sisters, one balanced, the other partial trisomic 10q].

Ann Genet. 1972 Jun;15(2):85-92.

[Partial trisomy 10 due to hereditary translocation t(1;10)(q44;q22)].[因遗传性易位t(1;10)(q44;q22)导致的10号染色体部分三体]

Humangenetik. 1973;18(4):321-7. doi: 10.1007/BF00291129.

[Giemsa-R-banding analysis of the trisomy 9p and report of a new case].9号染色体短臂三体的吉姆萨R显带分析及1例新病例报告

Humangenetik. 1973 Apr 16;18(2):129-38. doi: 10.1007/BF00291480.

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