共 31 条
- [23] Prenatal diagnosis and molecular cytogenetic characterization of a de novo unbalanced reciprocal translocation of der(9) t(9;14)(p24.2;q32.11) associated with 9p terminal deletion and 14q distal duplication TAIWANESE JOURNAL OF OBSTETRICS & GYNECOLOGY, 2016, 55 (04): : 596 - 601
- [24] A de novo duplication of chromosome 21q22.11 → qter associated with Down syndrome: Prenatal diagnosis, molecular cytogenetic characterization and fetal ultrasound findings TAIWANESE JOURNAL OF OBSTETRICS & GYNECOLOGY, 2011, 50 (04): : 492 - 498
- [27] Prenatal diagnosis of a 15q11.2-q14 deletion of paternal origin associated with increased nuchal translucency, mosaicism for de novo multiple unbalanced translocations involving 15q11-q14, 5qter, 15qter, 17pter and 3qter and Prader-Willi syndrome TAIWANESE JOURNAL OF OBSTETRICS & GYNECOLOGY, 2021, 60 (02): : 335 - 340
- [28] Prenatal diagnosis and molecular cytogenetic characterization of a de novo 4.858-Mb microdeletion in 15q14 associated with ACTC1 and MEIS2 haploinsufficiency and tetralogy of Fallot TAIWANESE JOURNAL OF OBSTETRICS & GYNECOLOGY, 2016, 55 (02): : 270 - 274
- [29] Molecular cytogenetic characterization of de novo concomitant distal 8p deletion of 8p23.3p23.1 and Xp and Xq deletion of Xp22.13q28 due to an unbalanced X;8 translocation detected by amniocentesis TAIWANESE JOURNAL OF OBSTETRICS & GYNECOLOGY, 2023, 62 (01): : 128 - 131
- [30] Molecular genetic characterization of a prenatally detected de novo interstitial deletion of chromosome 2q (2q31.1-q32.1) encompassing HOXD13, ZNF385B and ZNF804A associated with syndactyly and increased first-trimester nuchal translucency TAIWANESE JOURNAL OF OBSTETRICS & GYNECOLOGY, 2017, 56 (03): : 398 - 401