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The incomplete male.

作者信息

Savage M O, Grant D B

出版信息

Arch Dis Child. 1978 Sep;53(9):701-3. doi: 10.1136/adc.53.9.701.

DOI:10.1136/adc.53.9.701
PMID:363063
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1545105/
Abstract
摘要

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引用本文的文献

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2
Measurement of urine 17-oxogenic steroids, 17-hydroxycorticosteroids, and 17-oxosteroids has been superseded by better tests.尿17-生氧类固醇、17-羟皮质类固醇和17-氧类固醇的测定已被更好的检测方法所取代。
Br Med J (Clin Res Ed). 1985 Sep 21;291(6498):805-6. doi: 10.1136/bmj.291.6498.805.

本文引用的文献

1
Familial incomplete male pseudohermaphroditism, type 1. Evidence for androgen resistance and variable clinical manifestations in a family with the Reifenstein syndrome.1型家族性不完全性男性假两性畸形。Reifenstein综合征家族中雄激素抵抗及可变临床表现的证据。
N Engl J Med. 1974 May 16;290(20):1097-103. doi: 10.1056/NEJM197405162902001.
2
Source of the anti-Müllerian hormone synthesized by the fetal testis: Müllerian-inhibiting activity of fetal bovine Sertoli cells in tissue culture.
Pediatr Res. 1974 Dec;8(12):968-71. doi: 10.1203/00006450-197412000-00011.
3
Steroid 5alpha-reductase deficiency in man: an inherited form of male pseudohermaphroditism.人类类固醇5α-还原酶缺乏症：一种遗传性男性假两性畸形形式。
Science. 1974 Dec 27;186(4170):1213-5. doi: 10.1126/science.186.4170.1213.
4
Familial incomplete male pseudohermaphroditism, type 2. Decreased dihydrotestosterone formation in pseudovaginal perineoscrotal hypospadias.2型家族性不完全性男性假两性畸形。假性阴道会阴阴囊型尿道下裂中双氢睾酮生成减少。
N Engl J Med. 1974 Oct 31;291(18):944-9. doi: 10.1056/NEJM197410312911806.
5
Steroid 17,20-desmolase deficiency: a new cause of male pseudohermaphroditism.类固醇17,20-裂解酶缺乏症：男性假两性畸形的一个新病因。
Clin Endocrinol (Oxf). 1972 Oct;1(4):369-85. doi: 10.1111/j.1365-2265.1972.tb00407.x.
6
17-hydroxylation deficiency in man.人类17-羟化酶缺乏症
J Clin Invest. 1966 Dec;45(12):1946-54. doi: 10.1172/JCI105499.
7
Familial male pseudohermaphroditism with gynecomastia due to a testicular 17-ketosteroid reductase defect. I. Studies in vivo.因睾丸17-酮类固醇还原酶缺陷导致的伴有男性乳房发育的家族性男性假两性畸形。I. 体内研究。
J Clin Endocrinol Metab. 1971 May;32(5):604-10. doi: 10.1210/jcem-32-5-604.
8
A specific and rapid determination of human skin dihydrotestosterone cytosol receptor.
J Clin Endocrinol Metab. 1977 Aug;45(2):363-6. doi: 10.1210/jcem-45-2-363.
9
Partial androgen insensitivity: the Reifenstein syndrome revisited.部分雄激素不敏感：再探赖芬斯坦综合征
N Engl J Med. 1977 Aug 18;297(7):350-6. doi: 10.1056/NEJM197708182970703.
10
Male pseudohermaphroditism due to steroid 5-alpha-reductase deficiency.因类固醇5-α还原酶缺乏所致的男性假两性畸形。
Am J Med. 1977 Feb;62(2):170-91. doi: 10.1016/0002-9343(77)90313-8.