Li LH - Search Results

1

Long contiguous stretches of homozygosity in the human genome.

Li LH, Ho SF, Chen CH, Wei CY, Wong WC, Li LY, Hung SI, Chung WH, Pan WH, Lee MT, Tsai FJ, Chang CF, Wu JY, Chen YT. Li LH, et al. Among authors: li ly. Hum Mutat. 2006 Nov;27(11):1115-21. doi: 10.1002/humu.20399. Hum Mutat. 2006. PMID: 16955415

2

Type II collagen gene variants and inherited osteonecrosis of the femoral head.

Liu YF, Chen WM, Lin YF, Yang RC, Lin MW, Li LH, Chang YH, Jou YS, Lin PY, Su JS, Huang SF, Hsiao KJ, Fann CS, Hwang HW, Chen YT, Tsai SF. Liu YF, et al. Among authors: li lh. N Engl J Med. 2005 Jun 2;352(22):2294-301. doi: 10.1056/NEJMoa042480. N Engl J Med. 2005. PMID: 15930420 Free article.

3

MPDA: microarray pooled DNA analyzer.

Yang HC, Huang MC, Li LH, Lin CH, Yu AL, Diccianni MB, Wu JY, Chen YT, Fann CS. Yang HC, et al. Among authors: li lh. BMC Bioinformatics. 2008 Apr 15;9:196. doi: 10.1186/1471-2105-9-196. BMC Bioinformatics. 2008. PMID: 18412951 Free PMC article.

4

Genome-wide copy number analysis using copy number inferring tool (CNIT) and DNA pooling.

Lin CH, Huang MC, Li LH, Wu JY, Chen YT, Fann CS. Lin CH, et al. Among authors: li lh. Hum Mutat. 2008 Aug;29(8):1055-62. doi: 10.1002/humu.20760. Hum Mutat. 2008. PMID: 18470944

5

Nonparametric estimation of LOH using Affymetrix SNP genotyping arrays for unpaired samples.

Huggins R, Li LH, Lin YC, Yu AL, Yang HC. Huggins R, et al. Among authors: li lh. J Hum Genet. 2008;53(11-12):983-990. doi: 10.1007/s10038-008-0340-9. Epub 2008 Nov 7. J Hum Genet. 2008. PMID: 18989737

6

A large-scale survey of genetic copy number variations among Han Chinese residing in Taiwan.

Lin CH, Li LH, Ho SF, Chuang TP, Wu JY, Chen YT, Fann CS. Lin CH, et al. Among authors: li lh. BMC Genet. 2008 Dec 24;9:92. doi: 10.1186/1471-2156-9-92. BMC Genet. 2008. PMID: 19108714 Free PMC article.

7

Chromosomal and genetic alterations in human hepatocellular adenomas associated with type Ia glycogen storage disease.

Kishnani PS, Chuang TP, Bali D, Koeberl D, Austin S, Weinstein DA, Murphy E, Chen YT, Boyette K, Liu CH, Chen YT, Li LH. Kishnani PS, et al. Among authors: li lh. Hum Mol Genet. 2009 Dec 15;18(24):4781-90. doi: 10.1093/hmg/ddp441. Epub 2009 Sep 16. Hum Mol Genet. 2009. PMID: 19762333

8

A new familial insertion, ins(18;9)(q12.2;q33.1q31.1) with a 9q31.1-9q33.1 deletion in a girl with a cleft lip and palate.

Chien SC, Li YC, Li LH, Wu JY, Hsu PC, Shi SL, Tsai FJ, Lin CC. Chien SC, et al. Among authors: li lh, li yc. Am J Med Genet A. 2010 Jul;152A(7):1862-7. doi: 10.1002/ajmg.a.33452. Am J Med Genet A. 2010. PMID: 20583161 No abstract available.

9

A new analysis tool for individual-level allele frequency for genomic studies.

Yang HC, Lin HC, Huang MC, Li LH, Pan WH, Wu JY, Chen YT. Yang HC, et al. Among authors: li lh. BMC Genomics. 2010 Jul 5;11:415. doi: 10.1186/1471-2164-11-415. BMC Genomics. 2010. PMID: 20602748 Free PMC article.

10

Identification of a submicroscopic 3.2 Mb chromosomal 16q12.2-13 deletion in a child with short stature, mild developmental delay, and craniofacial anomalies, by high-density oligonucleotide array-a recognizable syndrome.

Chang CF, Li LH, Wang CH, Tsai FJ, Chen TC, Wu JY, Chen YT, Tsai AC. Chang CF, et al. Among authors: li lh. Am J Med Genet A. 2010 Sep;152A(9):2365-71. doi: 10.1002/ajmg.a.33580. Am J Med Genet A. 2010. PMID: 20803649

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 NCBI Filters

Text availability

Article attribute

Article type

Publication date

1,120 results

Search Page