PubMed for id: 120626

Year	Number of Results
1976	1
1983	1
1985	1
1986	1
1988	1
1989	1
1990	1
1993	1
1996	2
2000	1
2001	2
2006	1
2007	1
2011	1
2012	2
2013	1
2015	4
2016	2
2017	2
2018	1
2021	1
2022	4
2023	10
2024	462

1

[17 beta-hydroxysteroid dehydrogenase 3 deficiency due to novel compound heterozygous variants of HSD17B3 gene in a sib pair].

Wu S, Zheng B, Liu T, Zhu Z, Gu W, Liu Q. Wu S, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2021 Aug 10;38(8):787-790. doi: 10.3760/cma.j.cn511374-20200527-00392. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2021. PMID: 34365626 Chinese.

2

Pitfalls in hormonal diagnosis of 17-beta hydroxysteroid dehydrogenase III deficiency.

Khattab A, Yuen T, Yau M, Domenice S, Frade Costa EM, Diya K, Muhuri D, Pina CE, Nishi MY, Yang AC, de Mendonça BB, New MI. Khattab A, et al. J Pediatr Endocrinol Metab. 2015 May;28(5-6):623-8. doi: 10.1515/jpem-2014-0295. J Pediatr Endocrinol Metab. 2015. PMID: 25536660

3

Clinical and molecular spectrum of patients with 17β-hydroxysteroid dehydrogenase type 3 (17-β-HSD3) deficiency.

Castro CC, Guaragna-Filho G, Calais FL, Coeli FB, Leal IR, Cavalcante-Junior EF, Monlleó IL, Pereira SR, Silva RB, Gabiatti JR, Marques-de-Faria AP, Maciel-Guerra AT, Mello MP, Guerra-Junior G. Castro CC, et al. Arq Bras Endocrinol Metabol. 2012 Nov;56(8):533-9. doi: 10.1590/s0004-27302012000800012. Arq Bras Endocrinol Metabol. 2012. PMID: 23295294

4

17 beta-hydroxysteroid dehydrogenase 3 deficiency in the Mediterranean population.

Rosler A. Rosler A. Pediatr Endocrinol Rev. 2006 Aug;3 Suppl 3:455-61. Pediatr Endocrinol Rev. 2006. PMID: 17551466

5

Substitution mutation C268Y causes 17 beta-hydroxysteroid dehydrogenase 3 deficiency.

Lindqvist A, Hughes IA, Andersson S. Lindqvist A, et al. J Clin Endocrinol Metab. 2001 Feb;86(2):921-3. doi: 10.1210/jcem.86.2.7172. J Clin Endocrinol Metab. 2001. PMID: 11158067

6

Male pseudohermaphroditism due to 17 beta-hydroxysteroid dehydrogenase 3 deficiency. Diagnosis, psychological evaluation, and management.

Mendonca BB, Inacio M, Arnhold IJ, Costa EM, Bloise W, Martin RM, Denes FT, Silva FA, Andersson S, Lindqvist A, Wilson JD. Mendonca BB, et al. Medicine (Baltimore). 2000 Sep;79(5):299-309. doi: 10.1097/00005792-200009000-00003. Medicine (Baltimore). 2000. PMID: 11039078 Free article.

7

Molecular genetics and pathophysiology of 17 beta-hydroxysteroid dehydrogenase 3 deficiency.

Andersson S, Geissler WM, Wu L, Davis DL, Grumbach MM, New MI, Schwarz HP, Blethen SL, Mendonca BB, Bloise W, Witchel SF, Cutler GB Jr, Griffin JE, Wilson JD, Russel DW. Andersson S, et al. J Clin Endocrinol Metab. 1996 Jan;81(1):130-6. doi: 10.1210/jcem.81.1.8550739. J Clin Endocrinol Metab. 1996. PMID: 8550739 Free article.

8

Sibship with 17-ketosteroid reductase (17-KSR) deficiency and hypothyroidism. Lack of linkage of histocompatibility leucocyte antigen and 17-KSR loci.

Lanes R, Brown TR, de Bustos EG, Valverde B, Pieretti RB, Bianco N, Ortega G, Migeon CJ. Lanes R, et al. J Clin Endocrinol Metab. 1983 Jul;57(1):190-6. doi: 10.1210/jcem-57-1-190. J Clin Endocrinol Metab. 1983. PMID: 6574136

9

Male pseudohermaphroditism due to 17-ketoreductase deficiency: report of a case without gynecomastia and without vaginal pouch.

Caufriez A. Caufriez A. Am J Obstet Gynecol. 1986 Jan;154(1):148-9. doi: 10.1016/0002-9378(86)90413-8. Am J Obstet Gynecol. 1986. PMID: 3004217

10

Absent spermatogenesis despite early bilateral orchidopexy in 17-ketoreductase deficiency.

Dumić M, Plavsić V, Fattorini I, Ille J. Dumić M, et al. Horm Res. 1985;22(1-2):100-6. doi: 10.1159/000180080. Horm Res. 1985. PMID: 2863205

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