Hao N - 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: hao n. 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

Evaluation and Analysis of Absence of Homozygosity (AOH) Using Chromosome Analysis by Medium Coverage Whole Genome Sequencing (CMA-seq) in Prenatal Diagnosis.

Lü Y, Jiang Y, Zhou X, Hao N, Lü G, Guo X, Guo R, Liu W, Xu C, Chang J, Li M, Zhang H, Zhou J, Zhang WV, Qi Q. Lü Y, et al. Among authors: hao n. Diagnostics (Basel). 2023 Feb 2;13(3):560. doi: 10.3390/diagnostics13030560. Diagnostics (Basel). 2023. PMID: 36766665 Free PMC article.

3

The Application of Optical Genome Mapping (OGM) in Severe Short Stature Caused by Duplication of 15q14q21.3.

Ke X, Yang H, Pan H, Jiang Y, Li M, Zhang H, Hao N, Zhu H. Ke X, et al. Among authors: hao n. Genes (Basel). 2023 Apr 29;14(5):1016. doi: 10.3390/genes14051016. Genes (Basel). 2023. PMID: 37239376 Free PMC article.

4

Prenatal genetic diagnosis of disseminated infantile myofibromatosis: a case report and literature review.

Lü Y, Jiang Y, Wu H, Qi Q, Zhou X, Guo Q, Hao N, Liu J, Meng H. Lü Y, et al. Among authors: hao n. BMC Med Genomics. 2023 Aug 11;16(1):185. doi: 10.1186/s12920-023-01612-w. BMC Med Genomics. 2023. PMID: 37568122 Free PMC article. Review.

5

Detection of Mosaic Absence of Heterozygosity (AOH) Using Low-Pass Whole Genome Sequencing in Prenatal Diagnosis: A Preliminary Report.

Lü Y, Jiang Y, Zhou X, Hao N, Xu C, Guo R, Chang J, Li M, Zhang H, Zhou J, Zhang WV, Qi Q. Lü Y, et al. Among authors: hao n. Diagnostics (Basel). 2023 Sep 9;13(18):2895. doi: 10.3390/diagnostics13182895. Diagnostics (Basel). 2023. PMID: 37761262 Free PMC article.

6

Analysis of complex chromosomal rearrangement involving chromosome 6 via the integration of optical genomic mapping and molecular cytogenetic methodologies.

Hao N, Lou H, Li M, Zhang H, Chang J, Qi Q, Zhou X, Bai J, Guo J, Wang Y, Zhang Y, Jiang Y. Hao N, et al. J Hum Genet. 2024 Jan;69(1):3-11. doi: 10.1038/s10038-023-01197-3. Epub 2023 Oct 11. J Hum Genet. 2024. PMID: 37821671

7

Whole-genome sequencing analysis in fetal structural anomalies: novel phenotype-genotype discoveries.

Qi Q, Jiang Y, Zhou X, Lü Y, Xiao R, Bai J, Lou H, Sun W, Lian Y, Hao N, Li M, Chang J. Qi Q, et al. Among authors: hao n. Ultrasound Obstet Gynecol. 2024 May;63(5):664-671. doi: 10.1002/uog.27517. Epub 2024 Apr 15. Ultrasound Obstet Gynecol. 2024. PMID: 37842862

8

Contribution of uniparental disomy to fetal growth restriction: a whole-exome sequencing series in a prenatal setting.

Li M, Hao N, Jiang Y, Xue H, Dai Y, Wang M, Bai J, Lv Y, Qi Q, Zhou X. Li M, et al. Among authors: hao n. Sci Rep. 2024 Jan 2;14(1):238. doi: 10.1038/s41598-023-50584-5. Sci Rep. 2024. PMID: 38168635 Free PMC article.

9

Prenatal diagnosis of recurrent Kagami-Ogata syndrome inherited from a mother affected by Temple syndrome: a case report and literature review.

Yang X, Li M, Qi Q, Zhou X, Hao N, Lü Y, Jiang Y. Yang X, et al. Among authors: hao n. BMC Med Genomics. 2024 Aug 29;17(1):222. doi: 10.1186/s12920-024-01987-4. BMC Med Genomics. 2024. PMID: 39210340 Free PMC article. Review.

10

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. Among authors: hao n. Hum Genomics. 2024 Nov 28;18(1):133. doi: 10.1186/s40246-024-00697-3. Hum Genomics. 2024. PMID: 39609713 Free PMC 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

724 results

Search Page

Filters