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Li-Feng Chen

Showing results (121-130 of 163) with videos related to

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Gene|August 13, 2013
Prenatal diagnosis and molecular cytogenetic characterization of mosaic ring chromosome 13Chih-Ping Chen, Chin-Han Tsai, Schu-Rern Chern, et al.
Taiwanese Journal of Obstetrics & Gynecology|September 4, 2016
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 duplicationChih-Ping Chen, Chen-Ju Lin, Schu-Rern Chern, et al.
Taiwanese Journal of Obstetrics & Gynecology|December 16, 2017
Prenatal diagnosis of a 1.6-Mb 4p16.3 interstitial microdeletion encompassing FGFRL1 and TACC3 associated with bilateral cleft lip and palate of Wolf-Hirschhorn syndrome facial dysmorphism and short long bonesChih-Ping Chen, Chen-Yu Chen, Schu-Rern Chern, et al.
Prenatal Diagnosis|March 28, 2006
Prenatal diagnosis of low-level mosaicism for a small XIST-negative supernumerary ring X chromosome in a nondysmorphic male fetusChih-Ping Chen, Shuan-Pei Lin, Chyi-Chyang Lin, et al.
Taiwanese Journal of Obstetrics & Gynecology|November 9, 2010
Prenatal diagnosis and molecular cytogenetic characterization of a small supernumerary marker chromosome derived from chromosome 22Chih-Ping Chen, Chyi-Chyang Lin, Yi-Ning Su, et al.
Taiwanese Journal of Obstetrics & Gynecology|May 10, 2021
Prenatal diagnosis of maternal uniparental disomy 16 associated with mosaic trisomy 16 at amniocentesis, and pericardial effusion and intrauterine growth restriction in the fetusChih-Ping Chen, Tsang-Ming Ko, Schu-Rern Chern, et al.
Taiwanese Journal of Obstetrics & Gynecology|January 31, 2023
Molecular cytogenetic characterization of de novo concomitant proximal 21q deletion of 21q11.2q21.3 and distal Xp deletion of Xp22.33p22.2 due to an unbalanced X;21 translocation detected by amniocentesisChih-Ping Chen, Shin-Wen Chen, Chao-Yun Wu, et al.
Taiwanese Journal of Obstetrics & Gynecology|April 30, 2016
Prenatal diagnosis and molecular cytogenetic characterization of low-level true mosaicism for trisomy 21 using uncultured amniocytesChih-Ping Chen, Yeou-Lih Wang, Schu-Rern Chern, et al.
Prenatal Diagnosis|July 26, 2006
Prenatal diagnosis of congenital chylothorax associated with de novopartial trisomy 12q (12q21.2-->qter)Chih-Ping Chen, Tzu-Hao Wang, Schu-Rern Chern, et al.
Gene|February 14, 2013
Prenatal diagnosis of ring chromosome 2 with lissencephaly and 2p25.3 and 2q37.3 microdeletions detected using array comparative genomic hybridizationChih-Ping Chen, Chen-Ju Lin, Tung-Yao Chang, et al.
Pageof 17

Showing results (121-130 of 163) with videos related to

Sort By:
Pageof 17
Gene|August 13, 2013
Prenatal diagnosis and molecular cytogenetic characterization of mosaic ring chromosome 13Chih-Ping Chen, Chin-Han Tsai, Schu-Rern Chern, et al.
Taiwanese Journal of Obstetrics & Gynecology|September 4, 2016
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 duplicationChih-Ping Chen, Chen-Ju Lin, Schu-Rern Chern, et al.
Taiwanese Journal of Obstetrics & Gynecology|December 16, 2017
Prenatal diagnosis of a 1.6-Mb 4p16.3 interstitial microdeletion encompassing FGFRL1 and TACC3 associated with bilateral cleft lip and palate of Wolf-Hirschhorn syndrome facial dysmorphism and short long bonesChih-Ping Chen, Chen-Yu Chen, Schu-Rern Chern, et al.
Prenatal Diagnosis|March 28, 2006
Prenatal diagnosis of low-level mosaicism for a small XIST-negative supernumerary ring X chromosome in a nondysmorphic male fetusChih-Ping Chen, Shuan-Pei Lin, Chyi-Chyang Lin, et al.
Taiwanese Journal of Obstetrics & Gynecology|November 9, 2010
Prenatal diagnosis and molecular cytogenetic characterization of a small supernumerary marker chromosome derived from chromosome 22Chih-Ping Chen, Chyi-Chyang Lin, Yi-Ning Su, et al.
Taiwanese Journal of Obstetrics & Gynecology|May 10, 2021
Prenatal diagnosis of maternal uniparental disomy 16 associated with mosaic trisomy 16 at amniocentesis, and pericardial effusion and intrauterine growth restriction in the fetusChih-Ping Chen, Tsang-Ming Ko, Schu-Rern Chern, et al.
Taiwanese Journal of Obstetrics & Gynecology|January 31, 2023
Molecular cytogenetic characterization of de novo concomitant proximal 21q deletion of 21q11.2q21.3 and distal Xp deletion of Xp22.33p22.2 due to an unbalanced X;21 translocation detected by amniocentesisChih-Ping Chen, Shin-Wen Chen, Chao-Yun Wu, et al.
Taiwanese Journal of Obstetrics & Gynecology|April 30, 2016
Prenatal diagnosis and molecular cytogenetic characterization of low-level true mosaicism for trisomy 21 using uncultured amniocytesChih-Ping Chen, Yeou-Lih Wang, Schu-Rern Chern, et al.
Prenatal Diagnosis|July 26, 2006
Prenatal diagnosis of congenital chylothorax associated with de novopartial trisomy 12q (12q21.2-->qter)Chih-Ping Chen, Tzu-Hao Wang, Schu-Rern Chern, et al.
Gene|February 14, 2013
Prenatal diagnosis of ring chromosome 2 with lissencephaly and 2p25.3 and 2q37.3 microdeletions detected using array comparative genomic hybridizationChih-Ping Chen, Chen-Ju Lin, Tung-Yao Chang, et al.
Pageof 17