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
[J].
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
[J].
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
[J].
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
[J].
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
[J].
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
[J].
TAIWANESE JOURNAL OF OBSTETRICS & GYNECOLOGY,
2017, 56 (03)
:398-401