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Li-Feng Chen

Showing results (141-150 of 163) with videos related to

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Taiwanese Journal of Obstetrics & Gynecology|March 8, 2021
Prenatal diagnosis of low-level mosaicism for a small supernumerary marker chromosome derived from chromosome 9q (9q13-q21.33) in a pregnancy with a favorable outcome, and cytogenetic discrepancy between cultured amniocytes and uncultured amniocytesChih-Ping Chen, Liang-Ming Lo, Tsang-Ming Ko, 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 ultrasoundChih-Ping Chen, Shu-Yuan Chang, Yen-Ni Chen, 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 syndromeChih-Ping Chen, Chen-Ju Lin, Schu-Rern Chern, et al.
Gene|September 24, 2013
Chromosome 17p13.3 deletion syndrome: aCGH characterization, prenatal findings and diagnosis, and literature reviewChih-Ping Chen, Tung-Yao Chang, Wan-Yuo Guo, et al.
Taiwanese Journal of Obstetrics & Gynecology|August 17, 2010
Prenatal diagnosis and molecular cytogenetic characterization of a small supernumerary marker chromosome derived from chromosome 18 and associated with a reciprocal translocation involving chromosomes 17 and 18Chih-Ping Chen, Chyi-Chyang Lin, Yi-Ning Su, et al.
Taiwanese Journal of Obstetrics & Gynecology|May 15, 2010
Unbalanced and balanced heterologous acrocentric rearrangements involving chromosome 21 at amniocentesisChih-Ping Chen, Schu-Rern Chern, Pei-Chen Wu, et al.
Taiwanese Journal of Obstetrics & Gynecology|June 9, 2018
Higher male prevalence of chromosomal mosaicism detected by amniocentesisChen-Ju Lin, Shin-Wen Chen, Chih-Ping Chen, et al.
Taiwanese Journal of Obstetrics & Gynecology|April 29, 2014
Chromosomal deletions detected at amniocentesisChen-Ju Lin, Chih-Ping Chen, Shu-Chin Chien, et al.
Taiwanese Journal of Obstetrics & Gynecology|April 10, 2012
Unexplained shortening of the long bones in the third trimester as the only prenatal feature in a male fetus with 45,X/46,X,r(Y) mosaicismChih-Ping Chen, Yi-Ning Su, Ming Chen, et al.
Prenatal Diagnosis|February 14, 2006
Prenatal diagnosis of pure distal 18q deletionChih-Ping Chen, Schu-Rern Chern, Fang-Yu Hung, et al.
Pageof 17

Showing results (141-150 of 163) with videos related to

Sort By:
Pageof 17
Taiwanese Journal of Obstetrics & Gynecology|March 8, 2021
Prenatal diagnosis of low-level mosaicism for a small supernumerary marker chromosome derived from chromosome 9q (9q13-q21.33) in a pregnancy with a favorable outcome, and cytogenetic discrepancy between cultured amniocytes and uncultured amniocytesChih-Ping Chen, Liang-Ming Lo, Tsang-Ming Ko, 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 ultrasoundChih-Ping Chen, Shu-Yuan Chang, Yen-Ni Chen, 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 syndromeChih-Ping Chen, Chen-Ju Lin, Schu-Rern Chern, et al.
Gene|September 24, 2013
Chromosome 17p13.3 deletion syndrome: aCGH characterization, prenatal findings and diagnosis, and literature reviewChih-Ping Chen, Tung-Yao Chang, Wan-Yuo Guo, et al.
Taiwanese Journal of Obstetrics & Gynecology|August 17, 2010
Prenatal diagnosis and molecular cytogenetic characterization of a small supernumerary marker chromosome derived from chromosome 18 and associated with a reciprocal translocation involving chromosomes 17 and 18Chih-Ping Chen, Chyi-Chyang Lin, Yi-Ning Su, et al.
Taiwanese Journal of Obstetrics & Gynecology|May 15, 2010
Unbalanced and balanced heterologous acrocentric rearrangements involving chromosome 21 at amniocentesisChih-Ping Chen, Schu-Rern Chern, Pei-Chen Wu, et al.
Taiwanese Journal of Obstetrics & Gynecology|June 9, 2018
Higher male prevalence of chromosomal mosaicism detected by amniocentesisChen-Ju Lin, Shin-Wen Chen, Chih-Ping Chen, et al.
Taiwanese Journal of Obstetrics & Gynecology|April 29, 2014
Chromosomal deletions detected at amniocentesisChen-Ju Lin, Chih-Ping Chen, Shu-Chin Chien, et al.
Taiwanese Journal of Obstetrics & Gynecology|April 10, 2012
Unexplained shortening of the long bones in the third trimester as the only prenatal feature in a male fetus with 45,X/46,X,r(Y) mosaicismChih-Ping Chen, Yi-Ning Su, Ming Chen, et al.
Prenatal Diagnosis|February 14, 2006
Prenatal diagnosis of pure distal 18q deletionChih-Ping Chen, Schu-Rern Chern, Fang-Yu Hung, et al.
Pageof 17