| no |
title |
author |
magazine |
year |
volume |
issue |
page(s) |
type |
| 1 |
Abnormal methylation of ST8SIA4 in low-motility sperm: A genome-wide identification approach
|
Chang, Chia-Ching
|
|
|
64 |
4 |
p. 650-654
|
article
|
| 2 |
A prenatally diagnosed Klinefelter syndrome case of 46,XX/47,XXY mosaicism with partial deletion of Y chromosome
|
Okubo, Haruna
|
|
|
64 |
4 |
p. 707-710
|
article
|
| 3 |
“Armadillo” sign as a new prenatal ultrasound clue for Pierre Robin sequence
|
Yang, Tze-Yi
|
|
|
64 |
4 |
p. 749-751
|
article
|
| 4 |
Better pregnancy outcomes in women with day 2 or day 3 fresh embryo transfer when progesterone supplementation for luteal phase support is initiated on the day of oocyte retrieval
|
Lee, Chia-Chen
|
|
|
64 |
4 |
p. 637-642
|
article
|
| 5 |
Cervical cancer in Taiwan
|
Yang, Szu-Ting
|
|
|
64 |
4 |
p. 592-595
|
article
|
| 6 |
Comparison of motor imagery focused pelvic floor exercises and relaxation exercises for treating dysmenorrhea: A randomized controlled study
|
Koçoğlu, Selda
|
|
|
64 |
4 |
p. 671-677
|
article
|
| 7 |
Cytogenetic discrepancy between cultured amniocytes and uncultured amniocytes, perinatal progressive decrease of the trisomy 21 cell line and a favorable fetal outcome in a pregnancy with low-level mosaic trisomy 21 at amniocentesis
|
Chen, Chih-Ping
|
|
|
64 |
4 |
p. 723-725
|
article
|
| 8 |
Detection of a rare maternal 6q27 microduplication in a fetus with no phenotypic abnormalities
|
Wu, Ji
|
|
|
64 |
4 |
p. 745-746
|
article
|
| 9 |
Detection of mosaic 1q21.1 microdeletion in a fetus associated with megacystis and arthrogryposis of bilateral hands
|
Chen, Chih-Ping
|
|
|
64 |
4 |
p. 716-717
|
article
|
| 10 |
Diagnostic contribution of conventional and molecular karyotyping in congenital diaphragmatic hernia related copy number variations
|
Somayyeh Heidargholizadeh, G.
|
|
|
64 |
4 |
p. 678-686
|
article
|
| 11 |
Editorial Board
|
|
|
|
64 |
4 |
p. i-ii
|
article
|
| 12 |
Falloposcope for early screening of high-grade serous ovarian carcinoma
|
Burtman, Anthony D.
|
|
|
64 |
4 |
p. 625-628
|
article
|
| 13 |
Incidental detection of a familial 361-kb 9q34.3 microduplication encompassing EHMT1 and CACNA1B without apparently phenotypic abnormality
|
Chen, Chih-Ping
|
|
|
64 |
4 |
p. 726-728
|
article
|
| 14 |
Instruction for Authors
|
|
|
|
64 |
4 |
p. E1-E7
|
article
|
| 15 |
Is the far-advanced endometrial cancer curable?
|
Wang, Peng-Hui
|
|
|
64 |
4 |
p. 596-598
|
article
|
| 16 |
Is the less the better for early-stage low-risk cervical cancer?
|
Wang, Peng-Hui
|
|
|
64 |
4 |
p. 602-604
|
article
|
| 17 |
Locally advanced cervical cancer treatment: Immunotherapy or induction dose-dense chemotherapy?
|
Wang, Peng-Hui
|
|
|
64 |
4 |
p. 605-607
|
article
|
| 18 |
Low-level mosaicism for 45,X in 45,X/46,XY at amniocentesis associated with complete cytogenetic discrepancy between cultured amniocytes and uncultured amniocytes, perinatal progressive decrease of the 45,X cell line and a favorable fetal outcome
|
Chen, Chih-Ping
|
|
|
64 |
4 |
p. 733-734
|
article
|
| 19 |
Low-level mosaic trisomy 21 at amniocentesis in a pregnancy associated with an abnormal first-trimester maternal serum screening result, a favorable fetal outcome and postnatal decrease of the aneuploid cell line
|
Chen, Chih-Ping
|
|
|
64 |
4 |
p. 735-737
|
article
|
| 20 |
Low-level mosaic trisomy 12 at amniocentesis in a pregnancy associated with complete cytogenetic discrepancy between cultured amniocytes and uncultured amniocytes, perinatal progressive decrease of the aneuploid cell line and a favorable fetal outcome
|
Chen, Chih-Ping
|
|
|
64 |
4 |
p. 721-722
|
article
|
| 21 |
Low-level mosaic trisomy 21 at amniocentesis in a pregnancy with a favorable fetal outcome and a normal karyotype at birth
|
Chen, Chih-Ping
|
|
|
64 |
4 |
p. 741-744
|
article
|
| 22 |
Molecular subtyping and the 2023 FIGO staging in endometrial cancer: Redefining adjuvant therapy
|
Lin, Hao
|
|
|
64 |
4 |
p. 616-624
|
article
|
| 23 |
Obstetric and neonatal outcomes in pregnant women with left-sided valvular stenosis in a tertiary medical center in Taiwan
|
Lee, Hui-Ling
|
|
|
64 |
4 |
p. 655-661
|
article
|
| 24 |
OHVIRA syndrome: A case report treated with delayed diagnosis and multidisciplinary approaches
|
Akay, Emrullah
|
|
|
64 |
4 |
p. 693-699
|
article
|
| 25 |
PHLDA2 expression and promoter methylation in placental trophoblasts: Associations with preeclampsia development
|
Chen, Jie
|
|
|
64 |
4 |
p. 662-670
|
article
|
| 26 |
Placental mesenchymal dysplasia: A cause of intrauterine growth restriction and intrauterine death
|
Çobankent Aytekin, Esra
|
|
|
64 |
4 |
p. 643-649
|
article
|
| 27 |
Plateletpheresis for treating essential thrombocythemia that developed during pregnancy: A case report
|
Masuko, Naohisa
|
|
|
64 |
4 |
p. 703-706
|
article
|
| 28 |
Post-laparoscopic shoulder-tip pain (STP)
|
Wang, Peng-Hui
|
|
|
64 |
4 |
p. 589-591
|
article
|
| 29 |
Postpartum readmission associated with severe maternal morbidity: A systematic review
|
Huang, Wen-Chu
|
|
|
64 |
4 |
p. 629-636
|
article
|
| 30 |
Prenatal diagnosis and genetic counseling of a de novo 18q21.2 microdeletion associated with normal phenotype
|
Feng, Yuexiang
|
|
|
64 |
4 |
p. 755-757
|
article
|
| 31 |
Prenatal diagnosis and genetic counselling of a paternal inherited GLI3 frameshift deletion in a Chinese family
|
Mei, Ru
|
|
|
64 |
4 |
p. 747-748
|
article
|
| 32 |
Prenatal diagnosis and genetic counselling of monozygotic triplets with paternally inherited chromosome 15q11.2 microdeletion in a Chinese family
|
Liu, Bo
|
|
|
64 |
4 |
p. 758-760
|
article
|
| 33 |
Prenatal diagnosis of a familial 22q11.21 microduplication and mosaic trisomy 20 in a pregnancy with an asymptomatic father carrier and a favorable fetal outcome
|
Chen, Chih-Ping
|
|
|
64 |
4 |
p. 738-740
|
article
|
| 34 |
Prenatal diagnosis of a familial Xq27.1-q28 deletion with an asymptomatic mother carrier and no abnormality in the female fetus
|
Chen, Chih-Ping
|
|
|
64 |
4 |
p. 729-732
|
article
|
| 35 |
Recent advances in cervical cancer treatment: Innovations from early-stage to advanced disease
|
Lin, Hao
|
|
|
64 |
4 |
p. 608-615
|
article
|
| 36 |
Recurrent cesarean scar pregnancy successfully managed by laparoscopy: Case report and current trend
|
Lin, Jing Wang
|
|
|
64 |
4 |
p. 711-715
|
article
|
| 37 |
Risk factors for failed induction of labor: A retrospective study in a single, tertiary, perinatal-care center
|
Nariai, Maika
|
|
|
64 |
4 |
p. 687-692
|
article
|
| 38 |
Routine transvaginal ultrasound preceding mid-pregnancy fetal anatomical screening is a feasible and valuable tool in screening for vasa previa
|
Wu, Pei-Chen
|
|
|
64 |
4 |
p. 752-754
|
article
|
| 39 |
The decision for adjuvant therapy for early-stage high-risk endometrial cancer is in dilemma
|
Wang, Peng-Hui
|
|
|
64 |
4 |
p. 599-601
|
article
|
| 40 |
The first report of a successful birth by preimplantation genetic testing for leukodystrophy induced by IBA57 gene
|
Wang, Juan
|
|
|
64 |
4 |
p. 700-702
|
article
|
| 41 |
47,XYY/45,X at amniocentesis in a pregnancy associated with a favorable fetal outcome and perinatal progressive decrease of the 45,X cell line
|
Chen, Chih-Ping
|
|
|
64 |
4 |
p. 718-720
|
article
|
Journal description