Huang L - Search Results

1

FGFR3 gene mutation plus GRB10 gene duplication in a patient with achondroplasia plus growth delay with prenatal onset.

Yuan H, Huang L, Hu X, Li Q, Sun X, Xie Y, Kong S, Wang X. Yuan H, et al. Among authors: huang l. Orphanet J Rare Dis. 2016 Jul 2;11(1):89. doi: 10.1186/s13023-016-0465-4. Orphanet J Rare Dis. 2016. PMID: 27370225 Free PMC article.

2

[Prenatal diagnosis of achondroplasia].

Huang X, Huang LH, Fang Q, Chen ML, Zhou Y, Cai J, Chen BJ, Chen JH. Huang X, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2008 Aug;25(4):427-9. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2008. PMID: 18683143 Chinese.

3

Clinical and molecular cytogenetic studies of an unrecognised 22q11.2 deletion in three families.

Huang L, Xie Y, Zhou Y, Luo Y, Huang X, Xu Z, Cai D, Fang Q. Huang L, et al. Among authors: huang x. Exp Ther Med. 2015 Mar;9(3):823-828. doi: 10.3892/etm.2015.2200. Epub 2015 Jan 21. Exp Ther Med. 2015. PMID: 25667635 Free PMC article.

4

Prenatal diagnosis of submicroscopic chromosomal aberrations in fetuses with ventricular septal defects by chromosomal microarray-based analysis.

Du L, Xie HN, Huang LH, Xie YJ, Wu LH. Du L, et al. Among authors: huang lh. Prenat Diagn. 2016 Dec;36(13):1178-1184. doi: 10.1002/pd.4953. Epub 2016 Nov 21. Prenat Diagn. 2016. PMID: 27794163

5

Prenatal diagnosis of dent disease type I with a nonsense pathogenic variant in CLCN5: a case study.

Zhu R, Zhu M, Wang B, Chen E, Cai D, Yang Y, Liang Y, Su C, Wang D, Sun X, Huang L, Xie Y. Zhu R, et al. Among authors: huang l. BMC Med Genomics. 2024 Jan 24;17(1):34. doi: 10.1186/s12920-024-01809-7. BMC Med Genomics. 2024. PMID: 38267993 Free PMC article.

6

[Clinical study and prenatal diagnosis of fetus with shortened long bones].

Huang LH, Fang Q, Xie HN, Yang ZY, Yang YZ, Shi HJ, Huang X. Huang LH, et al. Zhonghua Yi Xue Za Zhi. 2007 Dec 4;87(45):3178-82. Zhonghua Yi Xue Za Zhi. 2007. PMID: 18399109 Chinese.

7

[Retrospective Analysis of Hematological Phenotypes in Patients with Gene Mutation and Deletion α-Thalassemia].

Xie WH, Huang LH, Yu XG, Huang H, Huang JM, Chen PS. Xie WH, et al. Zhongguo Shi Yan Xue Ye Xue Za Zhi. 2021 Aug;29(4):1262-1265. doi: 10.19746/j.cnki.issn.1009-2137.2021.04.038. Zhongguo Shi Yan Xue Ye Xue Za Zhi. 2021. PMID: 34362513 Chinese.

8

Differing Microdeletion Sizes and Breakpoints in Chromosome 7q11.23 in Williams-Beuren Syndrome Detected by Chromosomal Microarray Analysis.

Li L, Huang L, Luo Y, Huang X, Lin S, Fang Q. Li L, et al. Among authors: huang l, huang x. Mol Syndromol. 2016 Feb;6(6):268-75. doi: 10.1159/000443942. Epub 2016 Feb 2. Mol Syndromol. 2016. PMID: 27022327 Free PMC article.

9

Application of chromosomal microarray analysis in prenatal diagnosis of fetal growth restriction.

Zhu H, Lin S, Huang L, He Z, Huang X, Zhou Y, Fang Q, Luo Y. Zhu H, et al. Among authors: huang l, huang x. Prenat Diagn. 2016 Jul;36(7):686-92. doi: 10.1002/pd.4844. Epub 2016 Jun 21. Prenat Diagn. 2016. PMID: 27221052

10

Imprinting and Promoter Usage of Insulin-Like Growth Factor II in Twin Discordant Placenta.

Luo YM, Fang Q, Shi HJ, Huang LH, Liang RC, Zhuang GL. Luo YM, et al. Obstet Gynecol Int. 2010;2010:498574. doi: 10.1155/2010/498574. Epub 2010 Jun 22. Obstet Gynecol Int. 2010. PMID: 20613997 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

33,999 results

Search Page

Filters