Yao F - Search Results

1

Approach to the Patient: Diagnosis and Treatment with Growth Hormone of Turner Syndrome and its Variants.

Zhou Z, Qiang J, Hao N, Guo X, Yao F, Yang H, Jiang Y, Zhu H, Chen S, Pan H. Zhou Z, et al. Among authors: yao f. J Clin Endocrinol Metab. 2024 Oct 1:dgae648. doi: 10.1210/clinem/dgae648. Online ahead of print. J Clin Endocrinol Metab. 2024. PMID: 39351778

2

[Establishment of multiple quantitative fluorescent polymerase chain reaction assay and its application in rapid prenatal diagnosis of common chromosome aneuploidies].

Xu AQ, Bian XM, Liu JT, Yao FX, Zhang WM, Hao N, Zhou J. Xu AQ, et al. Zhonghua Fu Chan Ke Za Zhi. 2010 Jul;45(7):481-7. Zhonghua Fu Chan Ke Za Zhi. 2010. PMID: 21029597 Chinese.

3

Array-based comparative genomic hybridization is more informative than conventional karyotyping and fluorescence in situ hybridization in the analysis of first-trimester spontaneous abortion.

Gao J, Liu C, Yao F, Hao N, Zhou J, Zhou Q, Zhang L, Liu X, Bian X, Liu J. Gao J, et al. Among authors: yao f. Mol Cytogenet. 2012 Jul 16;5(1):33. doi: 10.1186/1755-8166-5-33. Mol Cytogenet. 2012. PMID: 22794168 Free PMC article.

4

Copy number variation sequencing-based prenatal diagnosis using cell-free fetal DNA in amniotic fluid.

Qi Q, Lu S, Zhou X, Yao F, Hao N, Yin G, Li W, Bai J, Li N, Cram DS. Qi Q, et al. Among authors: yao f. Prenat Diagn. 2016 Jun;36(6):576-83. doi: 10.1002/pd.4830. Epub 2016 May 17. Prenat Diagn. 2016. PMID: 27084671

5

[Pilot study of genetic counseling and prenatal diagnosis in androgen insensitivity syndrome: with 3 families reports].

Luo M, Jiang YL, Yao FX, Tian QJ. Luo M, et al. Among authors: yao fx. Zhonghua Fu Chan Ke Za Zhi. 2021 Apr 25;56(4):251-256. doi: 10.3760/cma.j.cn112141-20200817-00644. Zhonghua Fu Chan Ke Za Zhi. 2021. PMID: 33902236 Chinese.

6

Long-read sequencing enables comprehensive molecular genetic diagnosis of Fabry disease.

Yao F, Hao N, Li D, Zhang W, Zhou J, Qiu Z, Mao A, Meng W, Liu J. Yao F, et al. Hum Genomics. 2024 Nov 28;18(1):133. doi: 10.1186/s40246-024-00697-3. Hum Genomics. 2024. PMID: 39609713 Free PMC article.

7

A heterozygous mutation in RPGR associated with X-linked retinitis pigmentosa in a patient with Turner syndrome mosaicism (45,X/46,XX).

Zhou Q, Yao F, Wang F, Li H, Chen R, Sui R. Zhou Q, et al. Among authors: yao f. Am J Med Genet A. 2018 Jan;176(1):214-218. doi: 10.1002/ajmg.a.38501. Epub 2017 Nov 14. Am J Med Genet A. 2018. PMID: 29135076

8

Clinical characteristics and molecular etiology of partial 17α-hydroxylase deficiency diagnosed in 46,XX patients.

Zhang D, Yao F, Luo M, Wang Y, Tian T, Deng S, Tian Q. Zhang D, et al. Among authors: yao f. Front Endocrinol (Lausanne). 2022 Dec 15;13:978026. doi: 10.3389/fendo.2022.978026. eCollection 2022. Front Endocrinol (Lausanne). 2022. PMID: 36589849 Free PMC article.

9

A deletion variant Arg616 of androgen receptor in a Chinese family with complete androgen insensitivity syndrome.

Ding L, Zhang D, Yao F, Luo M, Deng S, Tian Q. Ding L, et al. Among authors: yao f. Front Genet. 2023 May 9;14:1140083. doi: 10.3389/fgene.2023.1140083. eCollection 2023. Front Genet. 2023. PMID: 37274790 Free PMC article.

10

Genotyping of a Chinese family with 46,XX and 46,XY 17-hydroxylase deficiency.

Tian Q, Yao F, Sha G, Huang S, Tseng H, Schindler AE. Tian Q, et al. Among authors: yao f. Gynecol Endocrinol. 2009 Aug;25(8):485-90. doi: 10.1080/09513590902898239. Gynecol Endocrinol. 2009. PMID: 19499410 Free article.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

2,383 results

Search Page

Filters