Xu J - Search Results

1

A girl with pervasive developmental disorder and complex chromosome rearrangement involving 8p and 10p.

Zwaigenbaum L, Sonnenberg LK, Heshka T, Eastwood S, Xu J. Zwaigenbaum L, et al. Among authors: xu j. J Autism Dev Disord. 2005 Jun;35(3):393-9. doi: 10.1007/s10803-005-3307-0. J Autism Dev Disord. 2005. PMID: 16119480

2

Wolf-Hirschorn syndrome resulting from partial monosomy 4p/trisomy 9p.

Xu J, Freeman V, Carter RF, Paes B, Heshka T, Nowaczyk JM. Xu J, et al. Am J Med Genet. 2000 Aug 14;93(4):285-9. doi: 10.1002/1096-8628(20000814)93:4<285::aid-ajmg6>3.0.co;2-n. Am J Med Genet. 2000. PMID: 10946354

3

Trisomy 16pter to 16q12.1 and monosomy 22pter to 22q11.2 resulting from adjacent-2 segregation of a maternal complex chromosome rearrangement.

Xu J, Chernos J, Roland B. Xu J, et al. Am J Med Genet. 1997 Dec 19;73(3):327-9. Am J Med Genet. 1997. PMID: 9415693

4

Paternal deletion 6q24.3: a new congenital anomaly syndrome associated with intrauterine growth failure, early developmental delay and characteristic facial appearance.

Nowaczyk MJ, Carter MT, Xu J, Huggins M, Raca G, Das S, Martin CL, Schwartz S, Rosenfield R, Waggoner DJ. Nowaczyk MJ, et al. Among authors: xu j. Am J Med Genet A. 2008 Feb 1;146A(3):354-60. doi: 10.1002/ajmg.a.32144. Am J Med Genet A. 2008. PMID: 18203180

5

De novo 1q32q44 duplication and distal 1q trisomy syndrome.

Nowaczyk MJ, Bayani J, Freeman V, Watts J, Squire J, Xu J. Nowaczyk MJ, et al. Among authors: xu j. Am J Med Genet A. 2003 Jul 15;120A(2):229-33. doi: 10.1002/ajmg.a.20028. Am J Med Genet A. 2003. PMID: 12833404 Review.

6

Sensitivity of multiple color spectral karyotyping in detecting small interchromosomal rearrangements.

Fan YS, Siu VM, Jung JH, Xu J. Fan YS, et al. Among authors: xu j. Genet Test. 2000;4(1):9-14. doi: 10.1089/109065700316417. Genet Test. 2000. PMID: 10794355

7

Advances in molecular cytogenetics for the evaluation of mental retardation.

Xu J, Chen Z. Xu J, et al. Am J Med Genet C Semin Med Genet. 2003 Feb 15;117C(1):15-24. doi: 10.1002/ajmg.c.10016. Am J Med Genet C Semin Med Genet. 2003. PMID: 12561054 Review.

8

Characterization of an interstitial deletion del(13)(q22q32) using microdissection and sequential FISH and G-banding.

Xu J, Chernos JE, Bernier F, Lowry RB. Xu J, et al. Genet Test. 2000;4(3):279-82. doi: 10.1089/10906570050501506. Genet Test. 2000. PMID: 11142759 Review.

9

False-positive prenatal diagnosis of trisomy 18 by interphase FISH: hybridization of chromosome 18 alpha-satellite DNA probe (D18Z1) to the heterochromatic region of chromosome 9.

Wei S, Siu VM, Decker A, Quigg MH, Roberson J, Xu J, Adeyinka A. Wei S, et al. Among authors: xu j. Prenat Diagn. 2007 Nov;27(11):1064-6. doi: 10.1002/pd.1819. Prenat Diagn. 2007. PMID: 17654752 No abstract available.

10

Is there a correlation between the proportion of cells with isodicentric Yp at amniocentesis and phenotypic sex?

Xu J, Siu VM. Xu J, et al. Prenat Diagn. 2010 Sep;30(9):839-44. doi: 10.1002/pd.2565. Prenat Diagn. 2010. PMID: 20658696

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