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Li-Feng Chen

Showing results (151-160 of 163) with videos related to

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Taiwanese Journal of Obstetrics & Gynecology|January 31, 2023
Mosaic trisomy 21 at amniocentesis associated with a favorable fetal outcome and perinatal progressive decrease of the trisomy 21 cell lineChih-Ping Chen, Shin-Wen Chen, Liang-Kai Wang, et al.
Taiwanese Journal of Obstetrics & Gynecology|April 13, 2011
Unbalanced reciprocal translocations at amniocentesisChih-Ping Chen, Pei-Chen Wu, Chen-Ju Lin, et al.
Taiwanese Journal of Obstetrics & Gynecology|October 28, 2011
Chromosome 15q overgrowth syndrome: prenatal diagnosis, molecular cytogenetic characterization, and perinatal findings in a fetus with dup(15)(q26.2q26.3)Chih-Ping Chen, Yi-Hui Lin, Heng-Kien Au, et al.
Taiwanese Journal of Obstetrics & Gynecology|October 9, 2012
Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from ring chromosome 2Chih-Ping Chen, Ming Chen, Schu-Rern Chern, et al.
Taiwanese Journal of Obstetrics & Gynecology|October 19, 2016
Prenatal diagnosis and molecular cytogenetic characterization of rec(10)dup(10p)inv(10)(p11.2q26.3) in a fetus associated with paternal pericentric inversionChih-Ping Chen, Tsang-Ming Ko, Yi-Ning Su, et al.
Gene|January 14, 2014
WITHDRAWN: Corrigendum to "Ring chromosome 21 presenting with sacrococcygeal teratoma: Prenatal diagnosis, molecular cytogenetic characterization and literature review" [Gene 522 (2013) 111-116]Chih-Ping Chen, Shuenn-Dyh Chang, Yi-Xuan Lee, et al.
Gene|August 13, 2013
Mosaic small supernumerary marker chromosome 1 at amniocentesis: prenatal diagnosis, molecular genetic analysis and literature reviewChih-Ping Chen, Ming Chen, Yi-Ning Su, et al.
Taiwanese Journal of Obstetrics & Gynecology|January 5, 2011
Balanced reciprocal translocations detected at amniocentesisChih-Ping Chen, Pei-Chen Wu, Chen-Ju Lin, et al.
Taiwanese Journal of Obstetrics & Gynecology|November 9, 2010
Mosaic trisomy 7 at amniocentesis: prenatal diagnosis and molecular genetic analysesChih-Ping Chen, Yi-Ning Su, Schu-Rern Chern, et al.
Taiwanese Journal of Obstetrics & Gynecology|October 22, 2018
Prenatal diagnosis of a familial 15q11.2 (BP1-BP2) microdeletion encompassing TUBGCP5, CYFIP1, NIPA2 and NIPA1 in a fetus with ventriculomegaly, microcephaly and intrauterine growth restriction on prenatal ultrasoundChih-Ping Chen, Shu-Yuan Chang, Liang-Kai Wang, et al.
Pageof 17

Showing results (151-160 of 163) with videos related to

Sort By:
Pageof 17
Taiwanese Journal of Obstetrics & Gynecology|January 31, 2023
Mosaic trisomy 21 at amniocentesis associated with a favorable fetal outcome and perinatal progressive decrease of the trisomy 21 cell lineChih-Ping Chen, Shin-Wen Chen, Liang-Kai Wang, et al.
Taiwanese Journal of Obstetrics & Gynecology|April 13, 2011
Unbalanced reciprocal translocations at amniocentesisChih-Ping Chen, Pei-Chen Wu, Chen-Ju Lin, et al.
Taiwanese Journal of Obstetrics & Gynecology|October 28, 2011
Chromosome 15q overgrowth syndrome: prenatal diagnosis, molecular cytogenetic characterization, and perinatal findings in a fetus with dup(15)(q26.2q26.3)Chih-Ping Chen, Yi-Hui Lin, Heng-Kien Au, et al.
Taiwanese Journal of Obstetrics & Gynecology|October 9, 2012
Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from ring chromosome 2Chih-Ping Chen, Ming Chen, Schu-Rern Chern, et al.
Taiwanese Journal of Obstetrics & Gynecology|October 19, 2016
Prenatal diagnosis and molecular cytogenetic characterization of rec(10)dup(10p)inv(10)(p11.2q26.3) in a fetus associated with paternal pericentric inversionChih-Ping Chen, Tsang-Ming Ko, Yi-Ning Su, et al.
Gene|January 14, 2014
WITHDRAWN: Corrigendum to "Ring chromosome 21 presenting with sacrococcygeal teratoma: Prenatal diagnosis, molecular cytogenetic characterization and literature review" [Gene 522 (2013) 111-116]Chih-Ping Chen, Shuenn-Dyh Chang, Yi-Xuan Lee, et al.
Gene|August 13, 2013
Mosaic small supernumerary marker chromosome 1 at amniocentesis: prenatal diagnosis, molecular genetic analysis and literature reviewChih-Ping Chen, Ming Chen, Yi-Ning Su, et al.
Taiwanese Journal of Obstetrics & Gynecology|January 5, 2011
Balanced reciprocal translocations detected at amniocentesisChih-Ping Chen, Pei-Chen Wu, Chen-Ju Lin, et al.
Taiwanese Journal of Obstetrics & Gynecology|November 9, 2010
Mosaic trisomy 7 at amniocentesis: prenatal diagnosis and molecular genetic analysesChih-Ping Chen, Yi-Ning Su, Schu-Rern Chern, et al.
Taiwanese Journal of Obstetrics & Gynecology|October 22, 2018
Prenatal diagnosis of a familial 15q11.2 (BP1-BP2) microdeletion encompassing TUBGCP5, CYFIP1, NIPA2 and NIPA1 in a fetus with ventriculomegaly, microcephaly and intrauterine growth restriction on prenatal ultrasoundChih-Ping Chen, Shu-Yuan Chang, Liang-Kai Wang, et al.
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