Identification of novel variants and candidate genes in women with 46,XX complete gonadal dysgenesis.
- Published in:
- Reproductive Biology & Endocrinology, 2024, v. 22, n. 1, p. 1, doi. 10.1186/s12958-024-01309-4
- By:
- Publication type:
- Article
Works by Tian, Qinjie
Results: 23
1
2
Diagnostic challenges and management advances in cytochrome P450 oxidoreductase deficiency, a rare form of congenital adrenal hyperplasia, with 46, XX karyotype.
- Published in:
- Frontiers in Endocrinology, 2023, p. 1, doi. 10.3389/fendo.2023.1226387
- By:
- Publication type:
- Article
3
Persistent megalocystic ovaries after ovarian hyperstimulation syndrome in a postpartum patient with polycystic ovarian syndrome: a case report.
- Published in:
- Journal of Ovarian Research, 2018, v. 11, n. 1, p. N.PAG, doi. 10.1186/s13048-018-0451-7
- By:
- Publication type:
- Article
4
Heavy menstrual bleeding among women aged 18-50 years living in Beijing, China: prevalence, risk factors, and impact on daily life.
- Published in:
- 2019
- By:
- Publication type:
- journal article
5
CYP17A1 mutations identified in 17 Chinese patients with 17α-hydroxylase/17,20-lyase deficiency.
- Published in:
- Gynecological Endocrinology, 2013, v. 29, n. 1, p. 10, doi. 10.3109/09513590.2012.705373
- By:
- Publication type:
- Article
6
Molecular study of five Chinese patients with 46XX partial 17a-hydroxylase/17,20-lyase deficiency.
- Published in:
- Gynecological Endocrinology, 2012, v. 28, n. 3, p. 234, doi. 10.3109/09513590.2011.593665
- By:
- Publication type:
- Article
7
Genotyping of a Chinese family with 46,XX and 46,XY 17-hydroxylase deficiency.
- Published in:
- Gynecological Endocrinology, 2009, v. 25, n. 8, p. 485, doi. 10.1080/09513590902898239
- By:
- Publication type:
- Article
8
Gender verification in athletes with disorders of sex development.
- Published in:
- Gynecological Endocrinology, 2009, v. 25, n. 2, p. 117, doi. 10.1080/09513590802530957
- By:
- Publication type:
- Article
9
Partial 17α-hydroxylase/17,20-lyase deficiency-clinical report of five Chinese 46,XX cases.
- Published in:
- Gynecological Endocrinology, 2008, v. 24, n. 7, p. 362, doi. 10.1080/09513590802194051
- By:
- Publication type:
- Article
10
Development of low-dose reproductive hormone therapies in China.
- Published in:
- Gynecological Endocrinology, 2006, v. 22, n. 11, p. 636, doi. 10.1080/09513590601005912
- By:
- Publication type:
- Article
11
The Investigation of Quality of Life in 87 Chinese Patients with Disorders of Sex Development.
- Published in:
- BioMed Research International, 2015, v. 2015, p. 1, doi. 10.1155/2015/342420
- By:
- Publication type:
- Article
12
A deletion variant Arg616 of androgen receptor in a Chinese family with complete androgen insensitivity syndrome.
- Published in:
- Frontiers in Genetics, 2023, p. 1, doi. 10.3389/fgene.2023.1140083
- By:
- Publication type:
- Article
13
Use and knowledge of the two FIGO systems for nongestational abnormal uterine bleeding in the reproductive years: A multinational survey.
- Published in:
- International Journal of Gynecology & Obstetrics, 2025, v. 168, n. 3, p. 1009, doi. 10.1002/ijgo.16138
- By:
- Publication type:
- Article
14
Genotype–Phenotype Correlation Analysis and Identification of a Novel SRD5A2 Mutation in Four Unrelated Chinese Patients with 5α-Reductase Deficiency.
- Published in:
- International Journal of General Medicine, 2022, v. 15, p. 6633, doi. 10.2147/IJGM.S377675
- By:
- Publication type:
- Article
15
Editorial: Non-classic congenital adrenal hyperplasia caused with common and rare forms: Unresolved issues and implications on clinical management.
- Published in:
- Frontiers in Endocrinology, 2023, v. 14, p. 01, doi. 10.3389/fendo.2023.1145352
- By:
- Publication type:
- Article
16
Ovarian gonadoblastoma with dysgerminoma in a girl with 46, XX karyotype 17a-hydroxylase/ 17, 20-lyase deficiency: A case report and literature review.
- Published in:
- Frontiers in Endocrinology, 2022, v. 13, p. 1, doi. 10.3389/fendo.2022.989695
- By:
- Publication type:
- Article
17
Gonadal Dominance and Internal Genitalia Phenotypes of Patients with Ovotesticular Disorders of Sex Development: Report of 22 Cases and Literature Review.
- Published in:
- Sexual Development, 2019, v. 13, n. 4, p. 187, doi. 10.1159/000507036
- By:
- Publication type:
- Article
18
Unmet needs in abnormal uterine bleeding due to ovulatory dysfunction.
- Published in:
- Gynecological Endocrinology, 2024, v. 40, n. 1, p. 1, doi. 10.1080/09513590.2024.2362244
- By:
- Publication type:
- Article
19
MYRF mutation leads to a single manifestation of sexual development and mimics partial androgen insensitivity syndrome: a case report and literature review.
- Published in:
- 2024
- By:
- Publication type:
- Case Study
20
Clinical characteristics and management of Turner patients with a small supernumerary marker chromosome.
- Published in:
- Gynecological Endocrinology, 2021, v. 37, n. 8, p. 730, doi. 10.1080/09513590.2021.1911992
- By:
- Publication type:
- Article
21
Evaluation and Management of Unexpected Functional Rudimentary Uteri in Mayer–Rokitansky–Küster–Hauser Syndrome of Chinese Women.
- Published in:
- BioMed Research International, 2020, p. 1, doi. 10.1155/2020/6808409
- By:
- Publication type:
- Article
22
Gonadal tumour risk in 292 phenotypic female patients with disorders of sex development containing Y chromosome or Y-derived sequence.
- Published in:
- Clinical Endocrinology, 2017, v. 86, n. 4, p. 621, doi. 10.1111/cen.13255
- By:
- Publication type:
- Article
23
The clinical diversity and molecular etiology in 46, XY disorders of sex development patients without uterus.
- Published in:
- Orphanet Journal of Rare Diseases, 2025, v. 20, n. 1, p. 1, doi. 10.1186/s13023-025-03719-y
- By:
- Publication type:
- Article