Li LY - Search Results

1

[Minute chromosome rearrangement detected by human telomeric band painting probes].

Qian WP, Tan YM, Tan YQ, Song D, Xu XQ, Li LY, Lu GX. Qian WP, et al. Among authors: li ly. Yi Chuan. 2006 May;28(5):518-20. Yi Chuan. 2006. PMID: 16735227 Chinese.

2

[Molecular cytogenetic detection of minute chromosomal structural abnormality on the chromosomal terminal regions].

Tan YQ, Li LY, Lu GX. Tan YQ, et al. Among authors: li ly. Yi Chuan Xue Bao. 2002 Sep;29(9):753-6. Yi Chuan Xue Bao. 2002. PMID: 12561219 Chinese.

3

[Molecular cytogenetic detection of partial chromosome 13q trisomy and its relation with the clinical features of tortilcollis].

Du J, Tan YQ, Li LY, Lu GX. Du J, et al. Among authors: li ly. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2003 Jun;20(3):189-92. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2003. PMID: 12778440 Chinese.

4

[Prenatal diagnosis of common chromosomal aneuploidies on uncultured amniotic fluid cells by fluorescence in situ hybridization].

Xiao HM, Tan YQ, Li LY, Lu GX. Xiao HM, et al. Among authors: li ly. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2004 Dec;21(6):608-10. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2004. PMID: 15583993 Chinese.

5

[Delineating a supernumerary marker chromosome by combining several cytogenetic and molecular cytogenetic techniques].

Tan YQ, Di YF, Song YZ, Cheng DH, Li LY, Lu GX. Tan YQ, et al. Among authors: li ly. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2007 Aug;24(4):392-6. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2007. PMID: 17680527 Chinese.

6

[Identification and characterization of marker chromosome in Turner syndrome].

Tan YQ, Cheng DH, DI YF, Li LY, Lu GX. Tan YQ, et al. Among authors: li ly. Zhonghua Fu Chan Ke Za Zhi. 2007 Oct;42(10):679-82. Zhonghua Fu Chan Ke Za Zhi. 2007. PMID: 18241543 Chinese.

7

Crypt Y chromosome fragment resulting from an X;Y translocation in a patient with premature ovarian failure.

Cheng DH, Tan YQ, Di YF, Li LY, Lu GX. Cheng DH, et al. Among authors: li ly. Fertil Steril. 2009 Aug;92(2):828.e3-6. doi: 10.1016/j.fertnstert.2008.07.014. Epub 2009 Jun 13. Fertil Steril. 2009. PMID: 19524892 Free article.

8

[Identification of a cryptic 1p36.3 microdeletion in a patient with Prader-Willi-like syndrome features].

Xu F, Cheng DH, Di YF, Tan K, Li LY, Lu GX, Tan YQ. Xu F, et al. Among authors: li ly. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2010 Oct;27(5):524-9. doi: 10.3760/cma.j.issn.1003-9406.2010.05.011. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2010. PMID: 20931530 Chinese.

9

[A de novo partial 5p deletion and cryptic 18p duplication detected by SNP-Array in a boy featuring Cri du Chat syndrome].

Hu JC, Tan K, Cheng DH, Li LY, Lu GX, Tan YQ. Hu JC, et al. Among authors: li ly. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2013 Feb;30(1):87-90. doi: 10.3760/cma.j.issn.1003-9406.2013.01.021. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2013. PMID: 23450488 Chinese.

10

[Advances in preimplantation genetic diagnosis for chromosomal translocation carrier].

Tan Y, Lu G, Li L. Tan Y, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2002 Feb;19(1):76-8. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2002. PMID: 11836695 Review. Chinese.

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