[Normal 46,XX daughter born to a 45,X/46,X,del(X)(q25) deletion (author's transl)]. - Suppr | 超能文献

[Normal 46,XX daughter born to a 45,X/46,X,del(X)(q25) deletion (author's transl)].

作者信息

de Grouchy J, Thibaud E, Turleau C, Roubin M, Rose F, Cachin O, Rappaport R

出版信息

Ann Genet. 1981;24(4):229-30.

Abstract

摘要

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[Normal 46,XX daughter born to a 45,X/46,X,del(X)(q25) deletion (author's transl)].

Ann Genet. 1981;24(4):229-30.

2

Ullrich-Turner syndrome in mother and daughter: prenatal diagnosis of a 46,X,del(X)(p21) offspring from a 45,X mother with low-level mosaicism for the del(X)(p21) in one ovary.母女患乌尔里希-特纳综合征：一名45,X母亲的一个卵巢存在低水平嵌合型del(X)(p21)，其46,X,del(X)(p21)后代的产前诊断

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3

[X short arm deletion and Turner syndrome. A new case 46, X, del (X) (p11) (author's transl)].

Ann Endocrinol (Paris). 1981 Apr-Jun;42(2):147-51.

4

Brief clinical report: del(X) (q26) in a phenotypically normal woman and her daughter who also has trisomy 21.

Am J Med Genet. 1983 Feb;14(2):367-72. doi: 10.1002/ajmg.1320140217.

5

Turner phenotype in mother and daughter.母亲和女儿的特纳氏综合征表型。

Obstet Gynecol. 1980 Dec;56(6):752-6.

6

[Iso-X chromosomes in primary amenorrhoea and Turner's syndrome - presentation by C-banding (author's transl)].[原发性闭经和特纳综合征中的等臂X染色体——C带显示（作者译）]

Zentralbl Gynakol. 1980;102(3):151-60.

7

[Multiple mosaicism in a patient with gonadal dysgenesis (author's transl)].性腺发育不全患者的多重镶嵌现象（作者译）

An Esp Pediatr. 1975 May-Jun;8(3):317-24.

8

Pregnancy in five women with 45,X/46,XX and 45,X/47,XXX gonadal dysgenesis.5名患有45,X/46,XX和45,X/47,XXX性腺发育不全女性的妊娠情况。

Birth Defects Orig Artic Ser. 1978;14(6C):171-84.

9

46, X, del (X) (p21) in a 14-year-old female with Turner signs, one streak and one normal ovary.一名14岁患有特纳氏体征的女性，染色体核型为46,X,del(X)(p21)，一侧为条索状性腺，另一侧为正常卵巢。

Ann Genet. 1981;24(2):114-6.

10

[Turner's syndrome in mother and daughter].[母女患特纳综合征]

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引用本文的文献

1

Deletion (X)(q26.1-->q28) in a proband and her mother: molecular characterization and phenotypic-karyotypic deductions.先证者及其母亲的X染色体缺失（X）（q26.1→q28）：分子特征分析及表型-核型推断

Am J Hum Genet. 1993 Mar;52(3):463-71.

2

X long-arm deletions. A review of non-mosaic cases studied with banding techniques.X染色体长臂缺失。对采用显带技术研究的非嵌合病例的综述。

Hum Genet. 1984;67(1):1-5. doi: 10.1007/BF00270550.

3

Chromosome studies in 2136 couples with spontaneous abortions.对2136对自然流产夫妇的染色体研究。

Hum Genet. 1986 Dec;74(4):399-401. doi: 10.1007/BF00280493.