共 8 条
- [1] Prenatal diagnosis of familial 17q11.2 duplication encompassing NF1 in a pregnancy associated with asymptomatic carrier parent TAIWANESE JOURNAL OF OBSTETRICS & GYNECOLOGY, 2024, 63 (03): : 426 - 427
- [2] Prenatal diagnosis of familial 2q13 microduplication and a de novo Xp22.33 microdeletion in a pregnancy associated with an asymptomatic mother carrier TAIWANESE JOURNAL OF OBSTETRICS & GYNECOLOGY, 2025, 64 (01): : 174 - 177
- [3] Recurrent 2q13 microduplication encompassing MALL, NPHP1, RGPD6, and BUB1 associated with autism spectrum disorder, intellectual disability, and liver disorder TAIWANESE JOURNAL OF OBSTETRICS & GYNECOLOGY, 2017, 56 (01): : 98 - 101
- [4] Prenatal diagnosis and molecular cytogenetic characterization of a de novo duplication of 2q12.2→q13 encompassing MALL, NPHP1, RGPD6 and BUB1 TAIWANESE JOURNAL OF OBSTETRICS & GYNECOLOGY, 2022, 61 (06): : 1044 - 1047
- [5] Prenatal diagnosis of familial 2p13.1-p12 microduplication in a pregnancy associated with asymptomatic carrier parent TAIWANESE JOURNAL OF OBSTETRICS & GYNECOLOGY, 2024, 63 (03): : 422 - 423
- [6] Prenatal diagnosis of a familial 736-kb Xp22.2p22.13 microduplication encompassing NHS associated with an asymptomatic father carrier and no abnormality in the fetus TAIWANESE JOURNAL OF OBSTETRICS & GYNECOLOGY, 2025, 64 (02): : 379 - 380
- [7] Prenatal diagnosis of a familial 21q22.3 microduplication encompassing part of Down syndrome critical region in a pregnancy associated with an asymptomatic mother carrier without Down syndrome phenotype TAIWANESE JOURNAL OF OBSTETRICS & GYNECOLOGY, 2025, 64 (02): : 383 - 384
- [8] Prenatal diagnosis of familial 3p26.3p25.3 deletion in a pregnancy associated with a favorable fetal outcome and asymptomatic carrier parent and family members in three generations JOURNAL OF STROKE & CEREBROVASCULAR DISEASES, 2024, 33 (09): : 561 - 564