Wu BL - Search Results

1

Development of a focused oligonucleotide-array comparative genomic hybridization chip for clinical diagnosis of genomic imbalance.

Shen Y, Irons M, Miller DT, Cheung SW, Lip V, Sheng X, Tomaszewicz K, Shao H, Fang H, Tang HS, Irons M, Walsh CA, Platt O, Gusella JF, Wu BL. Shen Y, et al. Among authors: wu bl. Clin Chem. 2007 Dec;53(12):2051-9. doi: 10.1373/clinchem.2007.090290. Epub 2007 Sep 27. Clin Chem. 2007. PMID: 17901113

2

Oligonucleotide microarrays for clinical diagnosis of copy number variation.

Miller DT, Shen Y, Wu BL. Miller DT, et al. Among authors: wu bl. Curr Protoc Hum Genet. 2008 Jul;Chapter 8:Unit 8.12. doi: 10.1002/0471142905.hg0812s58. Curr Protoc Hum Genet. 2008. PMID: 18633976

3

Microarray-based genomic DNA profiling technologies in clinical molecular diagnostics.

Shen Y, Wu BL. Shen Y, et al. Among authors: wu bl. Clin Chem. 2009 Apr;55(4):659-69. doi: 10.1373/clinchem.2008.112821. Epub 2009 Feb 20. Clin Chem. 2009. PMID: 19233918 Review.

4

Genetic testing for developmental delay: keep searching for an answer.

Miller DT, Shen Y, Harris DJ, Wu BL, Sobeih MM. Miller DT, et al. Among authors: wu bl. Clin Chem. 2009 Apr;55(4):827-30; discussion 830-2. doi: 10.1373/clinchem.2008.119438. Clin Chem. 2009. PMID: 19325017 No abstract available.

5

Large-scale medical resequencing for X-linked mental retardation.

Shen Y, Wu BL, Gusella JF. Shen Y, et al. Among authors: wu bl. Clin Chem. 2010 Mar;56(3):339-41. doi: 10.1373/clinchem.2009.135020. Epub 2009 Dec 29. Clin Chem. 2010. PMID: 20040618 No abstract available.

6

Oligonucleotide microarrays for clinical diagnosis of copy number variation and zygosity status.

Miller DT, Shen Y, Wu BL. Miller DT, et al. Among authors: wu bl. Curr Protoc Hum Genet. 2012 Jul;Chapter 8:Unit8.12. doi: 10.1002/0471142905.hg0812s74. Curr Protoc Hum Genet. 2012. PMID: 22786613

7

Use of a multiplex PCR/sequencing strategy to detect both connexin 30 (GJB6) 342 kb deletion and connexin 26 (GJB2) mutations in cases of childhood deafness.

Wu BL, Kenna M, Lip V, Irons M, Platt O. Wu BL, et al. Am J Med Genet A. 2003 Aug 30;121A(2):102-8. doi: 10.1002/ajmg.a.20210. Am J Med Genet A. 2003. PMID: 12910486

8

Detection of homozygous and heterozygous SMN deletions of spinal muscular atrophy in a single assay with multiplex ligation-dependent probe amplification.

Tomaszewicz K, Kang P, Wu BL. Tomaszewicz K, et al. Among authors: wu bl. Beijing Da Xue Xue Bao Yi Xue Ban. 2005 Feb 18;37(1):55-7. Beijing Da Xue Xue Bao Yi Xue Ban. 2005. PMID: 15719043 Free article.

9

Effectiveness of multiplex ligation-dependent probe amplification assay used for detecting deletion of Prader-Willi syndrome.

Shao H, Lip V, Wu BL. Shao H, et al. Among authors: wu bl. Beijing Da Xue Xue Bao Yi Xue Ban. 2005 Feb 18;37(1):64-7. Beijing Da Xue Xue Bao Yi Xue Ban. 2005. PMID: 15719045 Free article.

10

Association between microdeletion and microduplication at 16p11.2 and autism.

Weiss LA, Shen Y, Korn JM, Arking DE, Miller DT, Fossdal R, Saemundsen E, Stefansson H, Ferreira MA, Green T, Platt OS, Ruderfer DM, Walsh CA, Altshuler D, Chakravarti A, Tanzi RE, Stefansson K, Santangelo SL, Gusella JF, Sklar P, Wu BL, Daly MJ; Autism Consortium. Weiss LA, et al. Among authors: wu bl. N Engl J Med. 2008 Feb 14;358(7):667-75. doi: 10.1056/NEJMoa075974. Epub 2008 Jan 9. N Engl J Med. 2008. PMID: 18184952 Free article.

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