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Items: 1 to 20 of 27

1.

Etiology and Outcome of non-immune Hydrops Fetalis in Southern China: report of 1004 cases.

Meng D, Li Q, Hu X, Wang L, Tan S, Su J, Zhang Y, Sun W, Chen B, He S, Lin F, Xie B, Chen S, Agrawal PB, Luo S, Fu C.

Sci Rep. 2019 Jul 24;9(1):10726. doi: 10.1038/s41598-019-47050-6.

2.

State Transition for Statistical SLAM Using Planar Features in 3D Point Clouds.

Gostar AK, Fu C, Chuah W, Hossain MI, Tennakoon R, Bab-Hadiashar A, Hoseinnezhad R.

Sensors (Basel). 2019 Apr 3;19(7). pii: E1614. doi: 10.3390/s19071614.

3.

[Genetic testing and pregnancy outcome of 337 fetuses with urinary system anomalies].

Zeng S, Wang L, Luo S, Li Q, Qiu X, Gui C, Liu T, Wei H, Ma G, Fu C.

Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2019 Apr 10;36(4):306-309. doi: 10.3760/cma.j.issn.1003-9406.2019.04.004. Chinese.

PMID:
30950013
4.

Chromosomal microarray and whole exome sequencing identify genetic causes of congenital hypothyroidism with extra-thyroidal congenital malformations.

Fu C, Luo S, Zhang Y, Fan X, D'Gama AM, Zhang X, Zheng H, Su J, Li C, Luo J, Agrawal PB, Li Q, Chen S.

Clin Chim Acta. 2019 Feb;489:103-108. doi: 10.1016/j.cca.2018.11.035. Epub 2018 Nov 30.

PMID:
30508507
5.

Genetic Testing and Pregnancy Outcome Analysis of 362 Fetuses with Congenital Heart Disease Identified by Prenatal Ultrasound.

Luo S, Meng D, Li Q, Hu X, Chen Y, He C, Xie B, She S, Li Y, Fu C.

Arq Bras Cardiol. 2018 Oct;111(4):571-577. doi: 10.5935/abc.20180144. Epub 2018 Aug 20. English, Portuguese.

6.

Newborn screening of glucose-6-phosphate dehydrogenase deficiency in Guangxi, China: determination of optimal cutoff value to identify heterozygous female neonates.

Fu C, Luo S, Li Q, Xie B, Yang Q, Geng G, Lin C, Su J, Zhang Y, Wang J, Qin Z, Luo J, Chen S, Fan X.

Sci Rep. 2018 Jan 16;8(1):833. doi: 10.1038/s41598-017-17667-6.

7.

Mutation screening of the GLIS3 gene in a cohort of 592 Chinese patients with congenital hypothyroidism.

Fu C, Luo S, Long X, Li Y, She S, Hu X, Mo M, Wang Z, Chen Y, He C, Su J, Zhang Y, Lin F, Xie B, Li Q, Chen S.

Clin Chim Acta. 2018 Jan;476:38-43. doi: 10.1016/j.cca.2017.11.011. Epub 2017 Nov 13.

PMID:
29146476
8.

Mosaic UPD(7q)mat in a patient with silver Russell syndrome.

Su J, Wang J, Fan X, Fu C, Zhang S, Zhang Y, Qin Z, Li H, Luo J, Li C, Jiang T, Shen Y.

Mol Cytogenet. 2017 Oct 17;10:36. doi: 10.1186/s13039-017-0337-1. eCollection 2017.

9.

The incidence of congenital hypothyroidism (CH) in Guangxi, China and the predictors of permanent and transient CH.

Fu C, Luo S, Li Y, Li Q, Hu X, Li M, Zhang Y, Su J, Hu X, Chen Y, Wang J, Xie B, Luo J, Fan X, Chen S, Shen Y.

Endocr Connect. 2017 Nov;6(8):926-934. doi: 10.1530/EC-17-0289. Epub 2017 Oct 26.

10.

[Application of SNP-array technology in the genetic analysis of pediatric patients with growth retardation].

Luo S, Fu C, Zhang S, Wang J, Fan X, Luo J, Chen R, Hu X, Qin H, Li C, Ou S, Li Q, Chen S.

Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2017 Jun 10;34(3):321-326. doi: 10.3760/cma.j.issn.1003-9406.2017.03.002. Chinese.

PMID:
28604947
11.

Next-generation sequencing analysis of twelve known causative genes in congenital hypothyroidism.

Fan X, Fu C, Shen Y, Li C, Luo S, Li Q, Luo J, Su J, Zhang S, Hu X, Chen R, Gu X, Chen S.

Clin Chim Acta. 2017 May;468:76-80. doi: 10.1016/j.cca.2017.02.009. Epub 2017 Feb 16.

PMID:
28215547
12.

Next-generation sequencing analysis of TSHR in 384 Chinese subclinical congenital hypothyroidism (CH) and CH patients.

Fu C, Wang J, Luo S, Yang Q, Li Q, Zheng H, Hu X, Su J, Zhang S, Chen R, Luo J, Zhang Y, Shen Y, Wei H, Meng D, Gui B, Zeng Z, Fan X, Chen S.

Clin Chim Acta. 2016 Nov 1;462:127-132. doi: 10.1016/j.cca.2016.09.007. Epub 2016 Sep 13.

PMID:
27637299
13.

A rare occurrence of two large de novo duplications on 1q42-q44 and 9q21.12-q21.33.

Wang J, Fu C, Zhang S, Luo J, Ouyang L, Xie B, Sun W, He S, Su J, Hu X, Fei D, Chen R, Fan X, Ou S, Chen S, Shen Y.

Gene. 2016 Dec 5;594(1):59-65. doi: 10.1016/j.gene.2016.08.042. Epub 2016 Aug 31.

PMID:
27591971
14.

Maternal uniparental disomy 14 and mosaic trisomy 14 in a Chinese boy with moderate to severe intellectual disability.

Zhang S, Qin H, Wang J, OuYang L, Luo S, Fu C, Fan X, Su J, Chen R, Xie B, Hu X, Chen S, Shen Y.

Mol Cytogenet. 2016 Aug 24;9(1):66. doi: 10.1186/s13039-016-0274-4. eCollection 2016.

15.

A novel de novo microdeletion at 17q11.2 adjacent to NF1 gene associated with developmental delay, short stature, microcephaly and dysmorphic features.

Xie B, Fan X, Lei Y, Chen R, Wang J, Fu C, Yi S, Luo J, Zhang S, Yang Q, Chen S, Shen Y.

Mol Cytogenet. 2016 May 31;9:41. doi: 10.1186/s13039-016-0251-y. eCollection 2016.

16.

Mutation screening of the TPO gene in a cohort of 192 Chinese patients with congenital hypothyroidism.

Fu C, Xie B, Zhang S, Wang J, Luo S, Zheng H, Su J, Hu X, Chen R, Fan X, Luo J, Gu X, Chen S.

BMJ Open. 2016 May 12;6(5):e010719. doi: 10.1136/bmjopen-2015-010719.

17.

de novo interstitial deletions at the 11q23.3-q24.2 region.

Su J, Chen R, Luo J, Fan X, Fu C, Wang J, He S, Hu X, Zhang S, Yi S, Chen S, Shen Y.

Mol Cytogenet. 2016 May 5;9:39. doi: 10.1186/s13039-016-0247-7. eCollection 2016.

18.

Next-generation sequencing analysis of DUOX2 in 192 Chinese subclinical congenital hypothyroidism (SCH) and CH patients.

Fu C, Luo S, Zhang S, Wang J, Zheng H, Yang Q, Xie B, Hu X, Fan X, Luo J, Chen R, Su J, Shen Y, Gu X, Chen S.

Clin Chim Acta. 2016 Jul 1;458:30-4. doi: 10.1016/j.cca.2016.04.019. Epub 2016 Apr 21.

PMID:
27108200
19.

Mutation screening of the SLC26A4 gene in a cohort of 192 Chinese patients with congenital hypothyroidism.

Fu C, Zheng H, Zhang S, Chen Y, Su J, Wang J, Xie B, Hu X, Fan X, Luo J, Li C, Chen R, Shen Y, Chen S.

Arch Endocrinol Metab. 2016 Aug;60(4):323-7. doi: 10.1590/2359-3997000000108. Epub 2016 Feb 16.

20.

Thyroglobulin gene mutations in Chinese patients with congenital hypothyroidism.

Hu X, Chen R, Fu C, Fan X, Wang J, Qian J, Yi S, Li C, Luo J, Su J, Zhang S, Xie B, Zheng H, Lai Y, Chen Y, Li H, Gu X, Chen S, Shen Y.

Mol Cell Endocrinol. 2016 Mar 5;423:60-6. doi: 10.1016/j.mce.2016.01.007. Epub 2016 Jan 8.

PMID:
26777470

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