对患有性腺发育不全体征患者的中心片段和环状物进行放射自显影研究。 - Suppr

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Autoradiographic investigations of centric fragments and rings in patients with stigmata of gonadal dysgenesis.

作者信息

Cohen M M, Sandberg A A, Takagi N, MacGillivray M H

出版信息

Cytogenetics. 1967;6(3):254-67. doi: 10.1159/000129946.

DOI:10.1159/000129946

PMID:6040474

Abstract

摘要

相似文献

Autoradiographic investigations of centric fragments and rings in patients with stigmata of gonadal dysgenesis.对患有性腺发育不全体征患者的中心片段和环状物进行放射自显影研究。

Cytogenetics. 1967;6(3):254-67. doi: 10.1159/000129946.

[A case of gonadal dysgenesis with 45X-46XXqi mosaicism (autoradiographic study of chromosomes)].[一例具有45,X - 46,XX嵌合体的性腺发育不全病例（染色体放射自显影研究）]

Rev Lyon Med. 1970 Oct 15;19(15):631-8.

[45,X/46, XYnf/47, XYnfYnf/46, X, dic (Ynf) (q12) mosaicism in a female patient with gonadal dysgenesis and the stigmata of Turner's syndrome].[一名患有性腺发育不全及特纳综合征体征的女性患者存在[45,X/46, XYnf/47, XYnfYnf/46, X, dic (Ynf) (q12)]嵌合体]

Rev Clin Esp. 1991 Jun;189(1):23-5.

[Gonadal dysgenesis with an unusual structural anomaly in an X chromosome (45,X-46,XXq+)].[伴有X染色体异常结构异常（45,X-46,XXq+）的性腺发育不全]

Humangenetik. 1972;14(4):285-99. doi: 10.1007/BF00290170.

Pericentric inversion in a group D chromosome (13-15) associated with amenorrhea and gonadal dysgenesis.与闭经和性腺发育不全相关的D组染色体（13 - 15）臂间倒位。

Ann Hum Genet. 1967 May;30(4):313-23. doi: 10.1111/j.1469-1809.1967.tb00032.x.

[Gonadal dysgenesis with female phenotype].[具有女性表型的性腺发育不全]

Acta Paediatr Belg. 1969;23(6):331-72.

Atypical gonadal dysgenesis. A clinical and cytogenetical report of three patients.非典型性腺发育不全。三例患者的临床及细胞遗传学报告。

J Obstet Gynaecol Br Commonw. 1973 Aug;80(8):735-44. doi: 10.1111/j.1471-0528.1973.tb16060.x.

Gynecologic and cytogenetic aspects of gonadal agenesis and dysgenesis.性腺发育不全和发育异常的妇科及细胞遗传学方面

Obstet Gynecol. 1970 Sep;36(3):368-72.

Cytogenetic, clinical and genealogical analyses in a series of gonadal dysgenesis patients and their families.对一系列性腺发育不全患者及其家族进行的细胞遗传学、临床和系谱分析。

Humangenetik. 1971;13(2):126-43. doi: 10.1007/BF00295794.

[Chromatin-positive gonadal dysgenesis].

Rev Chil Pediatr. 1986 Nov-Dec;57(6):542-5.

引用本文的文献

Small marker X chromosomes lack the X inactivation center: implications for karyotype/phenotype correlations.小标记X染色体缺乏X染色体失活中心：对核型/表型相关性的影响。

Am J Hum Genet. 1994 Jul;55(1):87-95.

BrdU-Hoechst-Giemsa analysis of DNA replication in synchronized lymphocyte cultures. Study of human X and Y chromosomes.同步淋巴细胞培养物中DNA复制的BrdU-Hoechst-Giemsa分析。人类X和Y染色体研究。

Chromosoma. 1982;85(4):553-69. doi: 10.1007/BF00327350.

Multiple abnormalities due to possible genetic inactivation in an X-autosome translocation.X-常染色体易位中可能因基因失活导致的多种异常。

Am J Hum Genet. 1971 Jul;23(4):410-8.

Structural aberrations of the Y chromosome and the corresponding phenotype. Report of a case with the karotype 45,X-46,X,i(Yp).Y染色体的结构畸变及相应表型。一例核型为45,X-46,X,i(Yp)病例的报告。

Humangenetik. 1973;19(1):57-66. doi: 10.1007/BF00295235.

Abnormal X chromosomes in man: origin, behavior and effects.人类异常X染色体：起源、行为及影响

Humangenetik. 1974;25(1):1-16. doi: 10.1007/BF00281002.

Forty four probands with an additional "marker" chromosome.44名携带额外“标记”染色体的先证者。

Hum Genet. 1985;69(4):353-70. doi: 10.1007/BF00291656.

X;15 translocation in a retarded girl: X inactivation pattern and attempt to localise the hexosaminidase A and other loci.一名智力发育迟缓女孩的X;15易位：X染色体失活模式及对己糖胺酶A和其他基因座的定位尝试

J Med Genet. 1979 Aug;16(4):254-62. doi: 10.1136/jmg.16.4.254.

Late-replicating ring X-chromosomes identified by R-banding after BrdU pulse. Three new examples of mosaicism 45, XO/46, Xr(X).经BrdU脉冲处理后通过R显带鉴定出的晚期复制环状X染色体。45,XO/46,Xr(X)嵌合体的三个新实例。

Hum Genet. 1976 Sep 10;34(1):45-52. doi: 10.1007/BF00284433.

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