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3q26.31-q29 duplication and 9q34.3 microdeletion associated with omphalocele, ventricular septal defect, abnormal first-trimester maternal serum screening and increased nuchal translucency: prenatal diagnosis and aCGH characterization.
Chen CP, Lin CJ, Chen YY, Wang LK, Chern SR, Wu PS, Su JW, Chen LF, Town DD, Pan CW, Wang W. Chen CP, et al. Among authors: wang w, wang lk. Gene. 2013 Dec 10;532(1):80-6. doi: 10.1016/j.gene.2013.09.025. Epub 2013 Sep 18. Gene. 2013. PMID: 24055486 Review.
Detection of recurrent transmission of 17q12 microdeletion by array comparative genomic hybridization in a fetus with prenatally diagnosed hydronephrosis, hydroureter, and multicystic kidney, and variable clinical spectrum in the family.
Chen CP, Chang SD, Wang TH, Wang LK, Tsai JD, Liu YP, Chern SR, Wu PS, Su JW, Chen YT, Wang W. Chen CP, et al. Among authors: wang w, wang lk, wang th. Taiwan J Obstet Gynecol. 2013 Dec;52(4):551-7. doi: 10.1016/j.tjog.2013.10.017. Taiwan J Obstet Gynecol. 2013. PMID: 24411042 Free article.
426 results