克兰费尔特综合征患者中存在具有重复性染色质的XXXY性染色体复合体。 - Suppr

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超能文献

An XXXY sex chromosome complex in Klinefelter subjects with duplicated sex chromatin.

作者信息

CARR D H, BARR M L, PLUNKETT E R, GRUMBACH M M, MORISHIMA A, CHU E H

出版信息

J Clin Endocrinol Metab. 1961 May;21:491-505. doi: 10.1210/jcem-21-5-491.

DOI:10.1210/jcem-21-5-491

PMID:13690986

Abstract

摘要

相似文献

An XXXY sex chromosome complex in Klinefelter subjects with duplicated sex chromatin.克兰费尔特综合征患者中存在具有重复性染色质的XXXY性染色体复合体。

J Clin Endocrinol Metab. 1961 May;21:491-505. doi: 10.1210/jcem-21-5-491.

[Atypical Klinefelter's syndrome with XXXY-chromosomes].[伴有XXXY染色体的非典型克兰费尔特综合征]

Andrologie. 1972;4(3):269-75.

Sex chromosome abnormalities in mentally defective children. A case of XXXY Klinefelter's syndrome and a buccal smear survey in 743 institutionalized patients in Tokyo.智力缺陷儿童的性染色体异常。一例XXXY克兰费尔特综合征及对东京743名收容机构患者的口腔涂片调查。

Paediatr Univ Tokyo. 1965 Aug;11:41-6.

[NUMERICAL ALTERATIONS OF THE SEXUAL CHROMOSOMES].[性染色体的数值改变]

Med Clin (Barc). 1963 Jul;41:12-6.

[Karyotype 46,XY-47,XXY-48,XXXY in 2 cases of Klinefelter's syndrome].[两例克兰费尔特综合征患者的核型分别为46,XY - 47,XXY - 48,XXXY]

Ann Genet. 1970 Jun;13(2):117-9.

[CYTOGENETICS OF KLINEFELTER'S SYNDROME].[克兰费尔特综合征的细胞遗传学]

Rev Clin Esp. 1964 Apr 30;93:92-5.

Chromosome count in a hermaphrodite with some features of Klinefelter's syndrome.

Lancet. 1960 Oct 1;2(7153):736-9. doi: 10.1016/s0140-6736(60)91796-7.

THE XXYY VARIANT OF KLINEFELTER'S SYNDROME.克兰费尔特综合征的XXYY变异型

Can Med Assoc J. 1964 Feb 29;90(9):575-80.

[Psychopathology of case of Klinefelter's syndrome with chromosomal finding 48,XXXY (author's transl)].染色体核型为48，XXXY的克兰费尔特综合征病例的精神病理学（作者译）

Cesk Psychiatr. 1976 Jun;72(3):201-5.

[Cytogenetic studies in Klinefelter's syndrome with 47,XXY-48,XXXY karyotype].

Endokrynol Pol. 1972 May-Jun;23(3):267-81.

引用本文的文献

COEXISTING CRETINISM AND KLINEFELTER'S SYNDROME.先天性甲状腺功能减退症与克兰费尔特综合征并存

Br Med J. 1965 May 1;1(5443):1170. doi: 10.1136/bmj.1.5443.1170.

[ON THE CLINICAL ASPECTS AND HISTOPATHOLOGY OF PRIMARY MALE HYPOGONADISM. 2. CASTRATISM AND SO-CALLED KLINEFELTER'S SYNDROME AS DISEASE FORMS WITH KNOWN ETIOLOGY].[原发性男性性腺功能减退的临床特征与组织病理学。2. 去势及所谓克兰费尔特综合征作为病因明确的疾病形式]

Arch Klin Exp Dermatol. 1963 Sep 2;217:149-95.

XXXY chromosomal abnormality in a child.一名儿童的XXXY染色体异常。

Calif Med. 1970 Jan;112(1):30-2.

Abnormalities of human sex chromosomes. VI. Monozygotic twins with the complement 48,XXXY.

Humangenetik. 1974 Mar 28;21(4):301-8.

The influence of inactive chromosomes on human development. Anomalous sex chromosome complements and the phenotype.失活染色体对人类发育的影响。异常性染色体组成与表型。

Humangenetik. 1973;17(2):105-36. doi: 10.1007/BF00277906.

[XXXY Klinefelter's syndrome].

Humangenetik. 1972;15(4):327-33. doi: 10.1007/BF00281732.

Malformations of kidney and urinary tract in common chromosomal aberrations. II. Morphogenetic studies.常见染色体畸变中的肾和尿路畸形。II. 形态发生学研究。

Humangenetik. 1973 Mar 23;18(1):16-32. doi: 10.1007/BF00279027.

Hypothyroidism due to auto-immune thyroiditis in a young child with Down's syndrome.一名患有唐氏综合征的幼儿因自身免疫性甲状腺炎导致甲状腺功能减退。

Arch Dis Child. 1967 Aug;42(224):449-52. doi: 10.1136/adc.42.224.449.

Autoimmunity and chromosomal aberrations.自身免疫与染色体畸变。

Am J Hum Genet. 1966 Jan;18(1):93-108.

Sleep-wake behavior and integrated values of LH, FSH, PRL, FH and TSH in Klinefelter's syndrome.克兰费尔特综合征患者的睡眠-觉醒行为以及促黄体生成素、促卵泡生成素、催乳素、卵泡刺激素和促甲状腺激素的综合值

J Endocrinol Invest. 1979 Oct-Dec;2(4):385-93. doi: 10.1007/BF03349338.

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