Fu F - Search Results

1

[Analysis of 22 patients with congenital cleft lip and palate using high-resolution chromosome microarray].

Lei T, Zhang Y, Wang H, Li F, Cui Y, Fu F, Li R, Xie G, Zhang Y, Liao C. Lei T, et al. Among authors: fu f. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2014 Aug;31(4):433-7. doi: 10.3760/cma.j.issn.1003-9406.2014.04.005. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2014. PMID: 25119905 Chinese.

2

[Application of array-based comparative genomic hybridization in precise diagnosis of unbalanced chromosome aberration].

Fu F, Liao C, Pan M, Yi C, Liu H, Yuan S, Hu S, Zhong H, Li D. Fu F, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2010 Feb;27(1):47-51. doi: 10.3760/cma.j.issn.1003-9406.2010.01.010. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2010. PMID: 20140867 Chinese.

3

Ring chromosome 13 syndrome characterized by high resolution array based comparative genomic hybridization in patient with 47, XYY syndrome: a case report.

Liao C, Fu F, Zhang L. Liao C, et al. Among authors: fu f. J Med Case Rep. 2011 Mar 11;5:99. doi: 10.1186/1752-1947-5-99. J Med Case Rep. 2011. PMID: 21396087 Free PMC article.

4

Analysis of Chinese women with primary ovarian insufficiency by high resolution array-comparative genomic hybridization.

Liao C, Fu F, Yang X, Sun YM, Li DZ. Liao C, et al. Among authors: fu f. Chin Med J (Engl). 2011 Jun;124(11):1739-42. Chin Med J (Engl). 2011. PMID: 21740789

5

[Dandy-walker syndrome and microdeletions on chromosome 7].

Liao C, Fu F, Li R, Pan M, Yang X, Yi CX, Li J, Li DZ. Liao C, et al. Among authors: fu f. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2012 Feb;29(1):48-51. doi: 10.3760/cma.j.issn.1003-9406.2012.01.012. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2012. PMID: 22311491 Chinese.

6

Prenatal diagnosis and molecular characterization of a novel locus for Dandy-Walker malformation on chromosome 7p21.3.

Liao C, Fu F, Li R, Yang X, Xu Q, Li DZ. Liao C, et al. Among authors: fu f. Eur J Med Genet. 2012 Aug-Sep;55(8-9):472-5. doi: 10.1016/j.ejmg.2012.04.008. Epub 2012 May 19. Eur J Med Genet. 2012. PMID: 22617776

7

Prenatal diagnosis of an atypical 1q21.1 microdeletion and duplication associated with foetal urogenital abnormalities.

Liao C, Fu F, Yi CX, Li R, Yang X, Xu Q, Li DZ. Liao C, et al. Among authors: fu f. Gene. 2012 Oct 1;507(1):92-4. doi: 10.1016/j.gene.2012.07.008. Epub 2012 Jul 20. Gene. 2012. PMID: 22820078 No abstract available.

8

[Prenatal diagnosis of fetal urinary abnormalities and microdeletion on chromosome 1q21.1].

Fu F, Huang YH, Liao C, Li R, Feng SH, Mai QJ, Li WK. Fu F, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2012 Oct;29(5):505-9. doi: 10.3760/cma.j.issn.1003-9406.2012.05.001. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2012. PMID: 23042382 Chinese.

9

High-resolution array-comparative genomic hybridization profiling reveals 20q13.33 alterations associated with ovarian endometriosis.

Yang W, Zhang Y, Fu F, Li R. Yang W, et al. Among authors: fu f. Gynecol Endocrinol. 2013 Jun;29(6):603-7. doi: 10.3109/09513590.2013.788632. Gynecol Endocrinol. 2013. PMID: 23656391 Free article.

10

Loss-of-function variation in the DPP6 gene is associated with autosomal dominant microcephaly and mental retardation.

Liao C, Fu F, Li R, Yang WQ, Liao HY, Yan JR, Li J, Li SY, Yang X, Li DZ. Liao C, et al. Among authors: fu f. Eur J Med Genet. 2013 Sep;56(9):484-9. doi: 10.1016/j.ejmg.2013.06.008. Epub 2013 Jul 5. Eur J Med Genet. 2013. PMID: 23832105

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