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- [4] TERMINAL 2q DELETION AND PARTIAL TRISOMY CHROMOSOME 15q: A CLINICAL AND CYTOGENETIC STUDY GENETIC COUNSELING, 2014, 25 (02): : 151 - 158
- [5] Prenatal diagnosis and molecular cytogenetic characterization of de novo partial monosomy 3p (3p26.3 → pter) and partial trisomy 16q (16q23.1 → qter) TAIWANESE JOURNAL OF OBSTETRICS & GYNECOLOGY, 2016, 55 (02): : 288 - 292
- [8] DE-NOVO TANDEM DUPLICATION OF CHROMOSOME SEGMENT 22QLL-Q12 - CLINICAL, CYTOGENETIC, AND MOLECULAR CHARACTERIZATION AMERICAN JOURNAL OF MEDICAL GENETICS, 1995, 56 (03): : 296 - 299
- [9] De novo unbalanced translocation leading to monosomy 9p24.3p24.1 and trisomy 19q13.42q13.43 characterized by microarray-based comparative genomic hybridization in a child with partial cortical dysplasia and craniofacial dysmorphisms without trigonocephaly AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2013, 161A (03) : 632 - 636