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Ovotestes and XY sex reversal in a female with an interstitial 9q33.3-q34.1 deletion encompassing NR5A1 and LMX1B causing features of Genitopatellar syndrome.
Schlaubitz S, Yatsenko SA, Smith LD, Keller KL, Vissers LE, Scott DA, Cai WW, Reardon W, Abdul-Rahman OA, Lammer EJ, Lifchez CA, Magenis E, Veltman JA, Stankiewicz P, Zabel BU, Lee B. Schlaubitz S, et al. Among authors: cai ww. Am J Med Genet A. 2007 May 15;143A(10):1071-81. doi: 10.1002/ajmg.a.31685. Am J Med Genet A. 2007. PMID: 17431898
Identification of critical regions for clinical features of distal 10q deletion syndrome.
Yatsenko SA, Kruer MC, Bader PI, Corzo D, Schuette J, Keegan CE, Nowakowska B, Peacock S, Cai WW, Peiffer DA, Gunderson KL, Ou Z, Chinault AC, Cheung SW. Yatsenko SA, et al. Among authors: cai ww. Clin Genet. 2009 Jul;76(1):54-62. doi: 10.1111/j.1399-0004.2008.01115.x. Epub 2009 Jun 22. Clin Genet. 2009. PMID: 19558528 Free article.
Cryptic unbalanced translocation t(17;18)(p13.2;q22.3) identified by subtelomeric FISH and defined by array-based comparative genomic hybridization in a patient with mental retardation and dysmorphic features.
Hwang KS, Pearson MA, Stankiewicz P, Lennon PA, Cooper ML, Wu J, Ou Z, Cai WW, Patel A, Cheung SW. Hwang KS, et al. Among authors: cai ww. Am J Med Genet A. 2005 Aug 15;137(1):88-93. doi: 10.1002/ajmg.a.30858. Am J Med Genet A. 2005. PMID: 16015583
Congenital diaphragmatic hernia associated with duplication of 11q23-qter.
Klaassens M, Scott DA, van Dooren M, Hochstenbach R, Eussen HJ, Cai WW, Galjaard RJ, Wouters C, Poot M, Laudy J, Lee B, Tibboel D, de Klein A. Klaassens M, et al. Among authors: cai ww. Am J Med Genet A. 2006 Jul 15;140(14):1580-6. doi: 10.1002/ajmg.a.31321. Am J Med Genet A. 2006. PMID: 16770801 Free PMC article.
Engineering a mouse balancer chromosome.
Zheng B, Sage M, Cai WW, Thompson DM, Tavsanli BC, Cheah YC, Bradley A. Zheng B, et al. Among authors: cai ww. Nat Genet. 1999 Aug;22(4):375-8. doi: 10.1038/11949. Nat Genet. 1999. PMID: 10431243
148 results