[Partial 13 trisomy by maternal 46, XX, t (3; 13) (p 26; q 21) translocation].

Suppr

超能文献

作者信息

Stoll C, Halb A

出版信息

Pediatrie. 1974 Oct-Nov;29(7):725-9.

PMID:4456285

Abstract

摘要

相似文献

[Partial 13 trisomy by maternal 46, XX, t (3; 13) (p 26; q 21) translocation].

Pediatrie. 1974 Oct-Nov;29(7):725-9.

Inherited partial trisomy 2: 46,XX,1p+;t(1;2) (p36;q31).

Birth Defects Orig Artic Ser. 1975;11(5):177-9.

Two cases of partial trisomy 10q syndrome due to a familial 10;20 translocation.

Genet Couns. 2000;11(4):355-61.

[Trisomy due to transmitted translocation t(13 q , 14 q ). Estimation of recurrence risks].

Arch Fr Pediatr. 1971 Oct;28(8):865-74.

De novo balanced translocation: 46, XX, t(13;20)(q34;p 11).

Endocrinologie. 1978 Oct-Dec;16(4):295-8.

[Partial 10q trisomy (q24;q ter) caused by a balanced maternal translocation t(6;10)(q26;q24)].

An Esp Pediatr. 1982 Aug;17(2):125-9.

[Partial trisomy 14q II.--Partial trisomy 14q due to a maternal t(12; 14) (q24.4; q21)].

Ann Genet. 1975 Mar;18(1):41-4.

[12 p trisomy. A new case (author's transl)].

Ann Pediatr (Paris). 1980 Dec;27(10):695-9.

[A new case of trisomy 5p].

Genetika. 1985 Dec;21(12):2066-70.

Trisomy 6q22 leads to 6qter due to maternal 6;21 translocation. Case report review of the literature.

Ann Genet. 1983;26(4):243-6.

引用本文的文献

Nonrandom distribution of exchange points in patients with reciprocal translocations.

Hum Genet. 1980;56(1):89-93. doi: 10.1007/BF00281575.

The phenotype in partial 13q trisomies, apropos of a familial (13;15)(q22;q26) translocation.

Hum Genet. 1984;67(1):86-93. doi: 10.1007/BF00270563.

Phenotype-karyotype correlation in patients trisomic for various segments of chromosome 13.

J Med Genet. 1986 Aug;23(4):310-5. doi: 10.1136/jmg.23.4.310.

Further delineation of the clinical picture of trisomy for the distal segment of chromosome 13: report of three cases.

Hum Genet. 1976 Apr 15;32(1):1-12. doi: 10.1007/BF00569970.

A new case of trisomy for the distal part of 13q due to maternal translocation, t(9;13)(p21;q21).

Hum Genet. 1976 Aug 30;33(3):213-22. doi: 10.1007/BF00286845.

Ring chromosome 3 in a retarded boy.

Hum Genet. 1978 Jun 27;42(3):345-8. doi: 10.1007/BF00291318.

13q- syndrome. Family study.

Arch Dis Child. 1977 Dec;52(12):972-4. doi: 10.1136/adc.52.12.972.

文献AI研究员

20分钟写一篇综述，助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型，支持多种主流文档格式。

立即体验