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- [2] Detection of chromosome 5q interstitial deletion of 5q14.3-q31.1 by chromosome microarray analysis in a second-trimester fetus with multiple congenital anomalies and a literature review of chromosome 5q interstitial deletion syndrome TAIWANESE JOURNAL OF OBSTETRICS & GYNECOLOGY, 2024, 63 (06): : 918 - 921
- [3] Prenatal diagnosis and molecular cytogenetic characterization of de novo distal 5p deletion and distal 22q duplication TAIWANESE JOURNAL OF OBSTETRICS & GYNECOLOGY, 2020, 59 (01): : 140 - 145
- [4] DELETION OF CHROMOSOME 2Q24-Q31 CAUSES CHARACTERISTIC DIGITAL ANOMALIES - CASE-REPORT AND REVIEW AMERICAN JOURNAL OF MEDICAL GENETICS, 1995, 55 (02): : 155 - 160
- [8] Prenatal findings and molecular cytogenetic analyses of a de novo interstitial deletion of 1q23.3 encompassing PBX1 gene TAIWANESE JOURNAL OF OBSTETRICS & GYNECOLOGY, 2019, 58 (02): : 292 - 295
- [9] Prenatal diagnosis and molecular cytogenetic characterization of a de novo 3.19-Mb chromosome 14q32.13-q32.2 deletion of paternal origin TAIWANESE JOURNAL OF OBSTETRICS & GYNECOLOGY, 2020, 59 (05): : 766 - 769