Search research articles
Contact Us
Filters
Showing results (31-40 of 44) with videos related to
Page
of 5
Sort By:
Taiwanese Journal of Obstetrics & Gynecology
|
December 16, 2017
Prenatal diagnosis and molecular cytogenetic characterization of an interstitial deletion of 18q12.1-q12.3 encompassing DTNA, CELF4 and SETBP1
Chih-Ping Chen, Chih-Heng Hsieh, Schu-Rern Chern, et al.
Taiwanese Journal of Obstetrics & Gynecology
|
October 19, 2016
Molecular cytogenetic characterization of an inv dup(15) chromosome presenting as a small supernumerary marker chromosome associated with the inv dup(15) syndrome
Chih-Ping Chen, Shuan-Pei Lin, Schu-Rern Chern, et al.
Taiwanese Journal of Obstetrics & Gynecology
|
August 15, 2017
Detection of paternal uniparental disomy 9 in a neonate with prenatally detected mosaicism for a small supernumerary marker chromosome 9 and a supernumerary ring chromosome 9
Chih-Ping Chen, Ming Chen, Liang-Kai Wang, et al.
Taiwanese Journal of Obstetrics & Gynecology
|
December 16, 2017
Prenatal diagnosis and molecular cytogenetic characterization of low-level mosaicism for tetrasomy 18p at amniocentesis in a pregnancy with a favorable outcome
Chih-Ping Chen, Tsang-Ming Ko, Yi-Yung Chen, et al.
Taiwanese Journal of Obstetrics & Gynecology
|
October 22, 2018
Prenatal diagnosis of a familial 1q21.1-q21.2 microdeletion in a fetus with polydactyly of left foot on prenatal ultrasound
Chih-Ping Chen, Shu-Yuan Chang, Yen-Ni Chen, et al.
Taiwanese Journal of Obstetrics & Gynecology
|
October 22, 2018
Prenatal diagnosis of a familial 5p14.3-p14.1 deletion encompassing CDH18, CDH12, PMCHL1, PRDM9 and CDH10 in a fetus with congenital heart disease on prenatal ultrasound
Chih-Ping Chen, Shu-Yuan Chang, Chen-Ju Lin, et al.
Taiwanese Journal of Obstetrics & Gynecology
|
March 4, 2017
Molecular cytogenetic characterization of Jacobsen syndrome (11q23.3-q25 deletion) in a fetus associated with double outlet right ventricle, hypoplastic left heart syndrome and ductus venosus agenesis on prenatal ultrasound
Chih-Ping Chen, Liang-Kai Wang, Pei-Chen Wu, et al.
Taiwanese Journal of Obstetrics & Gynecology
|
June 26, 2016
Molecular cytogenetic characterization of inv dup del(8p) in a fetus associated with ventriculomegaly, hypoplastic left heart, polyhydramnios and intestinal obstruction
Chih-Ping Chen, Tsang-Ming Ko, Wen-Chu Huang, et al.
Taiwanese Journal of Obstetrics & Gynecology
|
February 21, 2018
Prenatal diagnosis of a 0.7-Mb 17p13.3 microdeletion encompassing YWHAE and CRK but not PAFAH1B1 in a fetus without ultrasound abnormalities
Chih-Ping Chen, Tsang-Ming Ko, Liang-Kai Wang, et al.
Taiwanese Journal of Obstetrics & Gynecology
|
December 17, 2014
Prenatal diagnosis and molecular cytogenetic characterization of a 1.07-Mb microdeletion at 5q35.2-q35.3 associated with NSD1 haploinsufficiency and Sotos syndrome
Chih-Ping Chen, Chen-Ju Lin, Schu-Rern Chern, et al.
Page
of 5
Search research articles
Search
Showing results (31-40 of 44) with videos related to
Sort By:
Page
of 5
Taiwanese Journal of Obstetrics & Gynecology
|
December 16, 2017
Prenatal diagnosis and molecular cytogenetic characterization of an interstitial deletion of 18q12.1-q12.3 encompassing DTNA, CELF4 and SETBP1
Chih-Ping Chen, Chih-Heng Hsieh, Schu-Rern Chern, et al.
Taiwanese Journal of Obstetrics & Gynecology
|
October 19, 2016
Molecular cytogenetic characterization of an inv dup(15) chromosome presenting as a small supernumerary marker chromosome associated with the inv dup(15) syndrome
Chih-Ping Chen, Shuan-Pei Lin, Schu-Rern Chern, et al.
Taiwanese Journal of Obstetrics & Gynecology
|
August 15, 2017
Detection of paternal uniparental disomy 9 in a neonate with prenatally detected mosaicism for a small supernumerary marker chromosome 9 and a supernumerary ring chromosome 9
Chih-Ping Chen, Ming Chen, Liang-Kai Wang, et al.
Taiwanese Journal of Obstetrics & Gynecology
|
December 16, 2017
Prenatal diagnosis and molecular cytogenetic characterization of low-level mosaicism for tetrasomy 18p at amniocentesis in a pregnancy with a favorable outcome
Chih-Ping Chen, Tsang-Ming Ko, Yi-Yung Chen, et al.
Taiwanese Journal of Obstetrics & Gynecology
|
October 22, 2018
Prenatal diagnosis of a familial 1q21.1-q21.2 microdeletion in a fetus with polydactyly of left foot on prenatal ultrasound
Chih-Ping Chen, Shu-Yuan Chang, Yen-Ni Chen, et al.
Taiwanese Journal of Obstetrics & Gynecology
|
October 22, 2018
Prenatal diagnosis of a familial 5p14.3-p14.1 deletion encompassing CDH18, CDH12, PMCHL1, PRDM9 and CDH10 in a fetus with congenital heart disease on prenatal ultrasound
Chih-Ping Chen, Shu-Yuan Chang, Chen-Ju Lin, et al.
Taiwanese Journal of Obstetrics & Gynecology
|
March 4, 2017
Molecular cytogenetic characterization of Jacobsen syndrome (11q23.3-q25 deletion) in a fetus associated with double outlet right ventricle, hypoplastic left heart syndrome and ductus venosus agenesis on prenatal ultrasound
Chih-Ping Chen, Liang-Kai Wang, Pei-Chen Wu, et al.
Taiwanese Journal of Obstetrics & Gynecology
|
June 26, 2016
Molecular cytogenetic characterization of inv dup del(8p) in a fetus associated with ventriculomegaly, hypoplastic left heart, polyhydramnios and intestinal obstruction
Chih-Ping Chen, Tsang-Ming Ko, Wen-Chu Huang, et al.
Taiwanese Journal of Obstetrics & Gynecology
|
February 21, 2018
Prenatal diagnosis of a 0.7-Mb 17p13.3 microdeletion encompassing YWHAE and CRK but not PAFAH1B1 in a fetus without ultrasound abnormalities
Chih-Ping Chen, Tsang-Ming Ko, Liang-Kai Wang, et al.
Taiwanese Journal of Obstetrics & Gynecology
|
December 17, 2014
Prenatal diagnosis and molecular cytogenetic characterization of a 1.07-Mb microdeletion at 5q35.2-q35.3 associated with NSD1 haploinsufficiency and Sotos syndrome
Chih-Ping Chen, Chen-Ju Lin, Schu-Rern Chern, et al.
Page
of 5