对因睾丸17-酮类固醇还原酶缺陷导致男性假两性畸形伴男性乳腺增生的进一步体内研究（与睾丸女性化病例相比）。 - Suppr

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超能文献

Further in vivo studies in male pseudohermaphroditism with gynecomastia due to a testicular 17-ketosteroid reductase defect (compared to a case of testicular feminization).

作者信息

Saez J M, Morera A M, De Peretti E, Bertrand J

出版信息

J Clin Endocrinol Metab. 1972 Mar;34(3):598-600. doi: 10.1210/jcem-34-3-598.

DOI:10.1210/jcem-34-3-598

PMID:4258797

Abstract

摘要

相似文献

Further in vivo studies in male pseudohermaphroditism with gynecomastia due to a testicular 17-ketosteroid reductase defect (compared to a case of testicular feminization).对因睾丸17-酮类固醇还原酶缺陷导致男性假两性畸形伴男性乳腺增生的进一步体内研究（与睾丸女性化病例相比）。

J Clin Endocrinol Metab. 1972 Mar;34(3):598-600. doi: 10.1210/jcem-34-3-598.

Familial male pseudohermaphroditism without gynecomastia due to deficient testicular 17-ketosteroid reductase activity.由于睾丸17-酮类固醇还原酶活性缺乏导致的无男子女性型乳房的家族性男性假两性畸形。

N Engl J Med. 1974 Oct 31;291(18):938-44. doi: 10.1056/NEJM197410312911805.

Children with male pseudohermaphroditism: endocrine and metabolic studies.男性假两性畸形患儿：内分泌与代谢研究

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Familial male pseudohermaphroditism with gynecomastia due to a testicular 17-ketosteroid reductase defect. I. Studies in vivo.

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