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1.
Research on THRβ gene mutation in a patient with thyroid hormone resistance syndrome using whole-exome sequencing / 中华内分泌代谢杂志
Chinese Journal of Endocrinology and Metabolism
; (12): 353-357, 2023.
Artículo
en Zh
| WPRIM | ID: wpr-994333
2.
Study on genetic etiology of two cases with hypophosphatasia(HPP) using whole-exome sequencing / 中华内分泌代谢杂志
Chinese Journal of Endocrinology and Metabolism
; (12): 950-956, 2022.
Artículo
en Zh
| WPRIM | ID: wpr-957637
3.
Molecular diagnosis and clinical features of 206 patients with 46, XY disorders of sexual development / 中华内分泌代谢杂志
Chinese Journal of Endocrinology and Metabolism
; (12): 781-788, 2022.
Artículo
en Zh
| WPRIM | ID: wpr-957615
4.
Clinical features and treatment outcome of four patients with Kallmann syndrome caused by fibroblast growth factor receptor-1 gene mutation / 中华内分泌代谢杂志
Chinese Journal of Endocrinology and Metabolism
; (12): 447-452, 2021.
Artículo
en Zh
| WPRIM | ID: wpr-885128
5.
DUOX2 mutations are frequently associated with congenital hypothyroidism in a Chinese Patients / 中华内分泌代谢杂志
Chinese Journal of Endocrinology and Metabolism
; (12): 567-573, 2017.
Artículo
en Zh
| WPRIM | ID: wpr-611587
6.
Effects of free fatty acids on catalytic activity of P450c17 in cultured NCI-H295R cells of adrenal gland / 中华内分泌代谢杂志
Chinese Journal of Endocrinology and Metabolism
; (12): 67-70, 2016.
Artículo
en Zh
| WPRIM | ID: wpr-491455
7.
Association of TSHR gene intron 1 and 4p14 single-nucleotide polymorphisms and gene-gene interactions with Graves′disease / 中华内分泌代谢杂志
Chinese Journal of Endocrinology and Metabolism
; (12): 292-297, 2016.
Artículo
en Zh
| WPRIM | ID: wpr-486847
8.
Association of the rs6832151 within chromosomal band 4p14 with Graves′disease / 中华内分泌代谢杂志
Chinese Journal of Endocrinology and Metabolism
; (12): 787-790, 2015.
Artículo
en Zh
| WPRIM | ID: wpr-478748
9.
SCGB3A2: A validated susceptibility gene to Graves' disease in different ethnic populations / 中华内分泌代谢杂志
Chinese Journal of Endocrinology and Metabolism
; (12): 93-96, 2013.
Artículo
en Zh
| WPRIM | ID: wpr-431223
10.
Progress of genetic studies on serum TSH levels / 中华内分泌代谢杂志
Chinese Journal of Endocrinology and Metabolism
; (12): 602-606, 2012.
Artículo
en Zh
| WPRIM | ID: wpr-427257
11.
SNPs in the SCGB3A2 promoter are associated with susceptibility to Graves' disease / 中华内分泌代谢杂志
Chinese Journal of Endocrinology and Metabolism
; (12): 989-993, 2012.
Artículo
en Zh
| WPRIM | ID: wpr-430363
12.
Influences of multiple gene interactions on bone mineral density and osteoporotic fractures in postmenopausal women / 中华内分泌代谢杂志
Chinese Journal of Endocrinology and Metabolism
; (12): 641-646, 2012.
Artículo
en Zh
| WPRIM | ID: wpr-424037
13.
Association of TSHR gene intron 1 polymorphisms with Graves′ disease / 中华内分泌代谢杂志
Chinese Journal of Endocrinology and Metabolism
; (12): 478-481, 2011.
Artículo
en Zh
| WPRIM | ID: wpr-416931
14.
Genetic diagnosis and weight loss surgery of a case of Prader-Willi syndrome / 中华内分泌代谢杂志
Chinese Journal of Endocrinology and Metabolism
; (12): 498-501, 2011.
Artículo
en Zh
| WPRIM | ID: wpr-416936
15.
Protein expression and preparation of polyclonal antibody of AD-004 and study on its expression in the adrenal and testis / 中华内分泌代谢杂志
Chinese Journal of Endocrinology and Metabolism
; (12)1986.
Artículo
en Zh
| WPRIM | ID: wpr-543696
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