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Taiwanese Journal of Obstetrics & Gynecology
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August 21, 2018
Prenatal diagnosis of a 3.2-Mb 2p16.1-p15 duplication associated with familial intellectual disability
Chih-Ping Chen, Schu-Rern Chern, Peih-Shan Wu, et al.
Taiwanese Journal of Obstetrics & Gynecology
|
August 15, 2017
Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 16
Chih-Ping Chen, Tsang-Ming Ko, Schu-Rern Chern, et al.
Taiwanese Journal of Obstetrics & Gynecology
|
January 2, 2017
Molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 8 or r(8)(::p11.22→q11.21::) in an 18-year-old female with short stature, obesity, attention deficit hyperactivity disorder, and intellectual disability
Chih-Ping Chen, Shuan-Pei Lin, Schu-Rern Chern, et al.
Journal of Experimental Botany
|
July 31, 2023
JustRNA: a database of plant long noncoding RNA expression profiles and functional network
Kuan-Chieh Tseng, Nai-Yun Wu, Chi-Nga Chow, 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 duplication
Chih-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 bones
Chih-Ping Chen, Chen-Yu Chen, Schu-Rern Chern, et al.
Taiwanese Journal of Obstetrics & Gynecology
|
October 19, 2016
Mosaic trisomy 17 at amniocentesis: Prenatal diagnosis, molecular genetic analysis, and literature review
Chih-Ping Chen, Liang-Kai Wang, Schu-Rern Chern, et al.
Taiwanese Journal of Obstetrics & Gynecology
|
April 20, 2017
Prenatal diagnosis and molecular cytogenetic characterization of concomitant familial small supernumerary marker chromosome derived from chromosome 4q (4q11.1-q13.2) and 5q13.2 microdeletion with no apparent phenotypic abnormality
Chih-Ping Chen, Schu-Rern Chern, Yen-Ni Chen, et al.
Taiwanese Journal of Obstetrics & Gynecology
|
January 2, 2017
Molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 8 or r(8)(::p12→q13.1::) associated with phenotypic abnormalities
Chih-Ping Chen, Shuan-Pei Lin, Yi-Hui Lin, 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 amniocytes
Chih-Ping Chen, Yeou-Lih Wang, Schu-Rern Chern, et al.
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of 5
Search research articles
Search
Showing results (21-30 of 44) with videos related to
Sort By:
Page
of 5
Taiwanese Journal of Obstetrics & Gynecology
|
August 21, 2018
Prenatal diagnosis of a 3.2-Mb 2p16.1-p15 duplication associated with familial intellectual disability
Chih-Ping Chen, Schu-Rern Chern, Peih-Shan Wu, et al.
Taiwanese Journal of Obstetrics & Gynecology
|
August 15, 2017
Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 16
Chih-Ping Chen, Tsang-Ming Ko, Schu-Rern Chern, et al.
Taiwanese Journal of Obstetrics & Gynecology
|
January 2, 2017
Molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 8 or r(8)(::p11.22→q11.21::) in an 18-year-old female with short stature, obesity, attention deficit hyperactivity disorder, and intellectual disability
Chih-Ping Chen, Shuan-Pei Lin, Schu-Rern Chern, et al.
Journal of Experimental Botany
|
July 31, 2023
JustRNA: a database of plant long noncoding RNA expression profiles and functional network
Kuan-Chieh Tseng, Nai-Yun Wu, Chi-Nga Chow, 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 duplication
Chih-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 bones
Chih-Ping Chen, Chen-Yu Chen, Schu-Rern Chern, et al.
Taiwanese Journal of Obstetrics & Gynecology
|
October 19, 2016
Mosaic trisomy 17 at amniocentesis: Prenatal diagnosis, molecular genetic analysis, and literature review
Chih-Ping Chen, Liang-Kai Wang, Schu-Rern Chern, et al.
Taiwanese Journal of Obstetrics & Gynecology
|
April 20, 2017
Prenatal diagnosis and molecular cytogenetic characterization of concomitant familial small supernumerary marker chromosome derived from chromosome 4q (4q11.1-q13.2) and 5q13.2 microdeletion with no apparent phenotypic abnormality
Chih-Ping Chen, Schu-Rern Chern, Yen-Ni Chen, et al.
Taiwanese Journal of Obstetrics & Gynecology
|
January 2, 2017
Molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 8 or r(8)(::p12→q13.1::) associated with phenotypic abnormalities
Chih-Ping Chen, Shuan-Pei Lin, Yi-Hui Lin, 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 amniocytes
Chih-Ping Chen, Yeou-Lih Wang, Schu-Rern Chern, et al.
Page
of 5