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Showing results 33 to 52 of 112
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Issue Date
Title
Author(s)
Source
scopus
WOS
Fulltext/Archive link
2005
Fetal OK-432 pleurodesis: Complete or incomplete? [2]
MING CHEN
; JIN-CHUNG SHIH
; Wang B.T.; Chen C.P.; CHIA-LI YU
Ultrasound in Obstetrics and Gynecology
29
40
1970
FGF21 in ataxia patients with spinocerebellar atrophy and mitochondrial disease
MING CHEN
Clinica Chimica Acta
12
12
2007
First prenatal exclusion of cystic fibrosis in East Asia
MING CHEN
Pediatrics International
0
0
2014
Generalized epilepsy in a patient with mosaic Turner syndrome: A case report
MING CHEN
Journal of Medical Case Reports
9
0
2009
Genetic evaluation and management of fetal chylothorax: Review and insights from a case of Noonan syndrome
Chen C.-H.; Chen T.-H.; Kuo S.-J.; Chen C.-P.; Lee D.-J.; Ke Y.-Y.; Yeh K.-T.; Ma G.-C.; Liu C.-S.; JIN-CHUNG SHIH
; MING CHEN
Lymphology
11
10
2014
Genome-wide normalized score: A novel algorithm to detect fetal trisomy 21 during non-invasive prenatal testing
Yeang C.H.; Ma G.C.; Hsu H.W.; Lin Y.S.; Chang S.M.; Cheng P.J.; CHI-AN CHEN
; YEN-HSUAN NI
; MING CHEN
Ultrasound in Obstetrics and Gynecology
12
12
2013
Genomic analyses of the Formosan harvest mouse (Micromys minutus) and comparisons to the brown Norway rat (Rattus norvegicus) and the house mouse (Mus musculus)
MING CHEN
Zoology
4
4
2006
Huge duplication cyst of small intestine: Ultrasonographic features and prenatal aspiration [2]
MING CHEN
Prenatal Diagnosis
1
0
2007
Interstitial deletion 13q31 associated with normal phenotype: Cytogenetic study of a family with concomitant segregation of reciprocal translocation and interstitial deletion
MING CHEN
Journal of the Formosan Medical Association
2
2
2011
Intrapartum uterine rupture associated with a scarred cervix because of a previous rupture of cystic cervical endometriosis
MING CHEN
Taiwanese Journal of Obstetrics and Gynecology
12
8
2012
Inv dup del(10q): Identification by fluorescence in situ hybridization and array comparative genomic hybridization in a fetus with two concurrent chromosomal rearrangements
MING CHEN
Taiwanese Journal of Obstetrics and Gynecology
4
2
2004
Invasive Fetal Therapy: Global Status and Local Development
MING CHEN
Taiwanese Journal of Obstetrics and Gynecology
2
0
2016
Late onset of large benign ductus arteriosus aneurysm presented with increased nuchal translucency and cystic hygroma at first trimester Down syndrome screening
MING CHEN
Taiwanese Journal of Obstetrics and Gynecology
0
0
2009
Late Termination of Pregnancy: Experience From an East Asian Population and Report of a Novel Technique for Feticide
Chen C.-H; Chen T.-H; Kuo S.-J; CHIN-DER CHEN
; YU-SHIH YANG
; MING CHEN
Journal of Medical Ultrasound
3
0
2015
Lessons learned from two missed prenatal cases of hemoglobin Bart’s hydrops fetalis until second trimester despite a nationwide screening program.
MING CHEN
HEREDITARY GENETICS: CURRENT RESEARCH
2016
Low-molecular-weight-heparin can benefit women with recurrent pregnancy loss and sole protein S deficiency: A historical control cohort study from Taiwan
MING-CHING SHEN
; Wu W.-J.; Cheng P.-J.; Ma G.-C.; Li W.-C.; Liou J.-D.; Chang C.-S.; Lin W.-H.; MING CHEN
Thrombosis Journal
12
0
2005
Management of oligohydramnios with antepartum amnioinfusion, amniopatch and cerclage
MING CHEN
; CHANG-YAO HSIEH
; Cameron A.D.; JIN-CHUNG SHIH
; CHIEN-NAN LEE
; HONG-NERNG HO
; Chen T.-H.; Chen C.-P.
Taiwanese Journal of Obstetrics and Gynecology
5
0
2014
Microdeletions/duplications involving TBX1 gene in fetuses with conotruncal heart defects which are negative for 22q11.2 deletion on fluorescence in-situ hybridization
MING CHEN
; YU-SHIH YANG
; JIN-CHUNG SHIH
; Lin W.-H.; Lee D.-J.; Lin Y.-S.; Chou C.-H.; Cameron A.D.; Ginsberg N.A.; CHI-AN CHEN
; Lee M.-L.; Ma G.-C.
Ultrasound in Obstetrics and Gynecology
20
21
2010
Mirror-image type D interrupted aortic arch: A novel cardiac phenotype providing some perspective in the del22q11.2 syndrome
Lee M.-L.; MING CHEN
; Yang A.D.; ING-SH CHIU
International Journal of Cardiology
2
1
2017
Molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 7 in the male partner of a phenotypically normal couple with repeated spontaneous abortions
MING CHEN
Taiwanese Journal of Obstetrics and Gynecology
0
0