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OVARIAN DYSGENESIS (TURNER'S SYNDROME). A CASE REPORT.

作者信息

JAMES W F

出版信息

J Natl Med Assoc. 1964 Nov;56(6):511-5.

PMID:14222913
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2610979/
Abstract
摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bf79/2610979/aea46789fe20/jnma00550-0047-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bf79/2610979/6ef88e94e90e/jnma00550-0046-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bf79/2610979/6a0b7b9c0645/jnma00550-0047-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bf79/2610979/aea46789fe20/jnma00550-0047-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bf79/2610979/6ef88e94e90e/jnma00550-0046-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bf79/2610979/6a0b7b9c0645/jnma00550-0047-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bf79/2610979/aea46789fe20/jnma00550-0047-b.jpg

相似文献

1
OVARIAN DYSGENESIS (TURNER'S SYNDROME). A CASE REPORT.卵巢发育不全(特纳综合征)。病例报告。
J Natl Med Assoc. 1964 Nov;56(6):511-5.
2
[GONADAL DYSGENESIS WITH FEMALE PHENOTYPE (TURNER'S SYNDROME)].[具有女性表型的性腺发育不全(特纳综合征)]
Rev Venez Sanid Asist Soc. 1963 Sep;28:277-304.
3
[Chromatography of the urinary 17-ketosteroids in Turner's syndrome].
Minerva Pediatr. 1962 Mar 24;14:323-4.
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[Metabolism of 17-ketosteroids in gonadal dysgenesis].[性腺发育不全中17-酮类固醇的代谢]
Rev Esp Obstet Ginecol. 1963 May-Jun;22:184-90.
5
DIMINISHED TESTICULAR FUNCTION IN "MALE TURNER'S SYNDROME".
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[ENDOCRINOLOGICAL STUDIES ON INTERSEX. 1. CHARACTERISTICS OF PATTERNS OF URINARY STEROIDS IN CASES OF TURNER'S SYNDROME, KLINEFELTER'S SYNDROME AND TESTICULAR FEMINIZATION SYNDROME].[两性畸形的内分泌学研究。1. 特纳综合征、克兰费尔特综合征和睾丸女性化综合征病例中尿甾体模式的特征]
Nihon Hinyokika Gakkai Zasshi. 1963 Jul;54:706-13.
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TURNER'S SYNDROME IN THE MALE.男性特纳综合征
Arch Intern Med. 1965 Jul;116:125-30. doi: 10.1001/archinte.1965.03870010127016.
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PURE GONADAL DYSGENESIS; REPORT OF A CASE.
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Urinary excretion of adrenal hormones in gonadal dysgenesis and its response to corticotrophin and gonadotrophin stimulation.性腺发育不全时肾上腺激素的尿排泄及其对促肾上腺皮质激素和促性腺激素刺激的反应。
Acta Endocrinol (Copenh). 1962 Jun;40:247-53. doi: 10.1530/acta.0.0400247.
10
[The fractionation of the 17-ketosteroids in some cases of the "congenital rudimentary gonad syndrome". II. Chromatograms in basal conditions].["先天性原始性腺综合征某些病例中17-酮类固醇的分级分离。II. 基础状态下的色谱图"]
Ann Ostet Ginecol. 1962 Apr;84:343-50.

本文引用的文献

1
Familial primary amenorrhea due to testicular feminization: A human gene affecting sex differenctiation.因睾丸女性化导致的家族性原发性闭经:一个影响性别分化的人类基因。
Proc Soc Exp Biol Med. 1960 Jan;103:192-6. doi: 10.3181/00379727-103-25456.
2
Smears from the oral mucosa in the detection of chromosomal sex.用于检测染色体性别的口腔黏膜涂片。
Lancet. 1955 Jul 9;269(6880):57-8. doi: 10.1016/s0140-6736(55)92161-9.
3
Cytogenetic studies in primary amenorrhoea.原发性闭经的细胞遗传学研究。
Lancet. 1961 Jun 3;1(7188):1183-9. doi: 10.1016/s0140-6736(61)91939-0.
4
The chromosomal etiology of congenital gonadal defects.先天性性腺缺陷的染色体病因学。
Am J Med. 1961 Apr;30:544-63. doi: 10.1016/0002-9343(61)90079-1.
5
A sex-chromosome anomaly in a case of gonadal dysgenesis (Turner's syndrome).一例性腺发育不全(特纳综合征)患者的性染色体异常。
Lancet. 1959 Apr 4;1(7075):711-3. doi: 10.1016/s0140-6736(59)91893-8.
6
Colour-blindness in ovarian agenesis (gonadal dysplasia).
Lancet. 1956 Jul 21;271(6934):118-20. doi: 10.1016/s0140-6736(56)90865-0.
7
Oral mucosal smears in detection of genetic sex.口腔黏膜涂片用于检测遗传性别。
J Am Med Assoc. 1956 Jun 23;161(8):683-5. doi: 10.1001/jama.1956.02970080013005.
8
Chromosomal sex in gonadal dysgenesis (ovarian agenesis): relationship to male pseudohermaphrodism and theories of human sex differentiation.
J Clin Endocrinol Metab. 1955 Oct;15(10):1161-93. doi: 10.1210/jcem-15-10-1161.
9
The detection of chromosomal sex in hermaphrodites from a skin biopsy.
Surg Gynecol Obstet. 1953 Jun;96(6):641-8.