Wu BL - Search Results

1

A recurrent 1.71 Mb genomic imbalance at 2q13 increases the risk of developmental delay and dysmorphism.

Yu HE, Hawash K, Picker J, Stoler J, Urion D, Wu BL, Shen Y. Yu HE, et al. Among authors: wu bl. Clin Genet. 2012 Mar;81(3):257-64. doi: 10.1111/j.1399-0004.2011.01637.x. Epub 2011 Feb 7. Clin Genet. 2012. PMID: 21255006

2

Microdeletion/duplication at 15q13.2q13.3 among individuals with features of autism and other neuropsychiatric disorders.

Miller DT, Shen Y, Weiss LA, Korn J, Anselm I, Bridgemohan C, Cox GF, Dickinson H, Gentile J, Harris DJ, Hegde V, Hundley R, Khwaja O, Kothare S, Luedke C, Nasir R, Poduri A, Prasad K, Raffalli P, Reinhard A, Smith SE, Sobeih MM, Soul JS, Stoler J, Takeoka M, Tan WH, Thakuria J, Wolff R, Yusupov R, Gusella JF, Daly MJ, Wu BL. Miller DT, et al. Among authors: wu bl. J Med Genet. 2009 Apr;46(4):242-8. doi: 10.1136/jmg.2008.059907. Epub 2008 Sep 19. J Med Genet. 2009. PMID: 18805830 Free PMC article.

3

Cytogenetic and molecular cytogenetic studies of a case of interstitial deletion of proximal 15q.

Tonk V, Wyandt HE, Osella P, Skare J, Wu BL, Haddad B, Milunsky A. Tonk V, et al. Among authors: wu bl. Clin Genet. 1995 Sep;48(3):151-5. doi: 10.1111/j.1399-0004.1995.tb04076.x. Clin Genet. 1995. PMID: 8556823 Review.

4

Genetic analysis of first-trimester miscarriages with a combination of cytogenetic karyotyping, microsatellite genotyping and arrayCGH.

Zhang YX, Zhang YP, Gu Y, Guan FJ, Li SL, Xie JS, Shen Y, Wu BL, Ju W, Jenkins EC, Brown WT, Zhong N. Zhang YX, et al. Among authors: wu bl. Clin Genet. 2009 Feb;75(2):133-40. doi: 10.1111/j.1399-0004.2008.01131.x. Clin Genet. 2009. PMID: 19215247

5

Distal 8p deletion (8)(p23.1): an easily missed chromosomal abnormality that may be associated with congenital heart defect and mental retardation.

Wu BL, Schneider GH, Sabatino DE, Bozovic LZ, Cao B, Korf BR. Wu BL, et al. Am J Med Genet. 1996 Mar 1;62(1):77-83. doi: 10.1002/(SICI)1096-8628(19960301)62:1<77::AID-AJMG16>3.0.CO;2-S. Am J Med Genet. 1996. PMID: 8779331

6

CHARGE association in a child with de novo inverted duplication (14)(q22-->q24.3).

North KN, Wu BL, Cao BN, Whiteman DA, Korf BR. North KN, et al. Among authors: wu bl. Am J Med Genet. 1995 Jul 17;57(4):610-4. doi: 10.1002/ajmg.1320570419. Am J Med Genet. 1995. PMID: 7573139

7

Deletion of the entire NF1 gene detected by the FISH: four deletion patients associated with severe manifestations.

Wu BL, Austin MA, Schneider GH, Boles RG, Korf BR. Wu BL, et al. Am J Med Genet. 1995 Dec 4;59(4):528-35. doi: 10.1002/ajmg.1320590427. Am J Med Genet. 1995. PMID: 8585580

8

Deletion of the entire NF1 gene causing distinct manifestations in a family.

Wu BL, Schneider GH, Korf BR. Wu BL, et al. Am J Med Genet. 1997 Mar 3;69(1):98-101. Am J Med Genet. 1997. PMID: 9066892

9

Localization of the gene for human heart fatty acid binding protein to chromosome 1p32-1p33.

Troxler RF, Offner GD, Jiang JW, Wu BL, Skare JC, Milunsky A, Wyandt HE. Troxler RF, et al. Among authors: wu bl. Hum Genet. 1993 Dec;92(6):563-6. doi: 10.1007/BF00420939. Hum Genet. 1993. PMID: 8262516

10

In situ hybridization applied to Waardenburg syndrome.

Wu BL, Milunsky A, Wyandt H, Hoth C, Baldwin C, Skare J. Wu BL, et al. Cytogenet Cell Genet. 1993;63(1):29-32. doi: 10.1159/000133495. Cytogenet Cell Genet. 1993. PMID: 8449034

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