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Prenatal diagnosis of partial trisomy 3p (3p21-->pter) and partial monosomy 11q (11q23-->qter) associated with abnormal sonographic findings of holoprosencephaly, orofacial clefts, pyelectasis and a unilateral duplex renal system.
Chen CP, Wang TH, Lin CC, Tsai FJ, Hsieh LJ, Wang W. Chen CP, et al. Among authors: lin cc. J Formos Med Assoc. 2008 Oct;107(10):822-6. doi: 10.1016/S0929-6646(08)60197-7. J Formos Med Assoc. 2008. PMID: 18926951 Free article.
Prenatal diagnosis and molecular cytogenetic characterization of a small supernumerary marker chromosome derived from chromosome 18 and associated with a reciprocal translocation involving chromosomes 17 and 18.
Chen CP, Lin CC, Su YN, Tsai FJ, Chen JT, Chern SR, Lee CC, Town DD, Chen LF, Wu PC, Wang W. Chen CP, et al. Among authors: lin cc. Taiwan J Obstet Gynecol. 2010 Jun;49(2):188-91. doi: 10.1016/S1028-4559(10)60039-3. Taiwan J Obstet Gynecol. 2010. PMID: 20708526 Free article.
6,673 results