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Klinefelter's syndrome. Clinical, endocrinological and cytogenetical studies.

作者信息

Froland A

出版信息

Dan Med Bull. 1969 May;16:Suppl 6:1-108.

PMID:5376065
Abstract
摘要

相似文献

1
Klinefelter's syndrome. Clinical, endocrinological and cytogenetical studies.克兰费尔特综合征。临床、内分泌及细胞遗传学研究。
Dan Med Bull. 1969 May;16:Suppl 6:1-108.
2
[Klinefelter's syndrome. Clinical, laboratory, psychiatric, cytogenetic and histopathologic study of 28 personal cases].
Minerva Med. 1974 Mar 14;65(19):1009-31.
3
[Klinefelter's syndrome. Clinical, psychiatric and cytogenetic findings in 28 cases].
MMW Munch Med Wochenschr. 1974 Sep 20;116(38):1601-8.
4
Klinefelter's syndrome and the XXY syndrome. A genetical, endocrinological and psychiatric-psychological study of thirty-three severely hypogonadal male patients and two patients with karyotype 47,XYY.克兰费尔特综合征与XXY综合征。对33例严重性腺功能减退男性患者及2例核型为47,XYY患者的遗传学、内分泌学及精神心理研究。
Acta Psychiatr Scand Suppl. 1969;209:1-353.
5
Klinefelter's syndrome and the XYY syndrome. A genetical, endocrinological and psychiatric-psychological study of thirty-three severely hypogonadal male patients and two patients with karyotype 47,XYY.克兰费尔特综合征与XYY综合征。对33名严重性腺功能减退男性患者及2名核型为47,XYY的患者进行的遗传学、内分泌学及精神心理学研究。
Acta Psychiatr Scand Suppl. 1969;209:1-353.
6
[Deliquency and gonosomic anomalies. Apropos of a subject with the karyotype 46,XY-47,XXY-48,XXXY].
J Genet Hum. 1974 Mar;22(1):61-71.
7
Mixed testicular dysgenesis and 46,XY-47,XXY mosaicism.混合性睾丸发育不全与46,XY-47,XXY嵌合体。
Clin Genet. 1973;4(2):130-3.
8
Cytogenetics and fluorescence in situ hybridization assessment of sex-chromosome mosaicism in Klinefelter's syndrome.克兰费尔特综合征中性染色体嵌合体的细胞遗传学和荧光原位杂交评估
Ann Genet. 2004 Apr-Jun;47(2):163-75. doi: 10.1016/j.anngen.2003.08.024.
9
[Klinefelter's syndrome. (Clinical case)].
Policlinico Med. 1971 Sep-Oct;78(5):195-205.
10
Sex chromosome aberrations in childhood. I. XXY and XXY mosaicism.
Acta Paediatr Acad Sci Hung. 1971;12(3):323-37.

引用本文的文献

1
Comparative single-cell analysis of biopsies clarifies pathogenic mechanisms in Klinefelter syndrome.对活检进行比较单细胞分析可阐明克氏综合征的发病机制。
Am J Hum Genet. 2021 Oct 7;108(10):1924-1945. doi: 10.1016/j.ajhg.2021.09.001.
2
Puberty in 24 patients with Klinefelter syndrome.24例克兰费尔特综合征患者的青春期情况。
Eur J Pediatr. 1982 Sep;139(1):8-12. doi: 10.1007/BF00442070.
3
Uveal coloboma and true Klinefelter syndrome.葡萄膜缺损和真性克兰费尔特综合征。
J Med Genet. 1970 Sep;7(3):213-23. doi: 10.1136/jmg.7.3.213.
4
Abnormalities of human sex chromosomes. VI. Monozygotic twins with the complement 48,XXXY.
Humangenetik. 1974 Mar 28;21(4):301-8.
5
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.
6
The effect of maternal age on the incidence of Down's syndrome.
Humangenetik. 1972;16(1):141-6. doi: 10.1007/BF00394000.
7
Follow-up 20 years later of 34 Klinefelter males with karyotype 47,XXY and 16 hypogonadal males with karyotype 46,XY.对34名核型为47,XXY的克兰费尔特综合征男性和16名核型为46,XY的性腺功能减退男性进行了20年后的随访。
Hum Genet. 1987 Oct;77(2):188-92. doi: 10.1007/BF00272390.
8
Studies of malformation syndromes in man XXXX: multiple congenital anomalies/mental retardation syndrome or variant familial developmental pattern; differential diagnosis and description of the McDonough syndrome (with XXY son from XY/XXY father).人类畸形综合征的研究XXXX:多重先天性异常/智力发育迟缓综合征或变异型家族性发育模式;麦克多诺综合征的鉴别诊断及描述(父亲为XY/XXY,儿子为XXY)
Z Kinderheilkd. 1975 Nov 13;120(4):231-42. doi: 10.1007/BF00440262.
9
Male hypogonadism.男性性腺功能减退
West J Med. 1976 Jun;124(6):446-75.
10
Testicular size and shape of 47,XYY and 47,XXY men in a double-blind, double-matched population survey.在一项双盲、双匹配的人群调查中,47,XYY和47,XXY男性的睾丸大小和形状
Am J Hum Genet. 1979 Nov;31(6):697-703.