Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Shuan-Pei Lin

Showing results (141-150 of 281) with videos related to

Pageof 29
Sort By:
Gene|April 13, 2013
6p21.2-p12.3 deletion detected by aCGH in an 8-year-old girl with cleidocranial dysplasia and developmental delayChih-Ping Chen, Shuan-Pei Lin, Yu-Peng Liu, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|May 20, 2008
Genetic analysis of mucopolysaccharidosis type VI in Taiwanese patientsWei-De Lin, Shuan-Pei Lin, Chung-Hsing Wang, 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 disabilityChih-Ping Chen, Shuan-Pei Lin, Schu-Rern Chern, et al.
Taiwanese Journal of Obstetrics & Gynecology|April 29, 2014
Interphase FISH on uncultured amniocytes at repeat amniocentesis for rapid diagnosis of true mosaicism in a case of level II mosaicism involving trisomy 21 in a single colony from an in situ culture of amniocytesChih-Ping Chen, Pu-Tsui Wang, Shuan-Pei Lin, et al.
European Journal of Medical Genetics|June 15, 2010
A de novo 7.9 Mb deletion in 22q13.2→qter in a boy with autistic features, epilepsy, developmental delay, atopic dermatitis and abnormal immunological findingsChih-Ping Chen, Shuan-Pei Lin, Schu-Rern Chern, et al.
Journal of Human Genetics|July 16, 2010
Mutation spectrum of MMACHC in Chinese patients with combined methylmalonic aciduria and homocystinuriaMei-Ying Liu, Yan-Ling Yang, Ying-Chen Chang, et al.
Taiwanese Journal of Obstetrics & Gynecology|April 10, 2012
Rapid aneuploidy diagnosis of partial trisomy 7q (7q34→qter) and partial monosomy 10q (10q26.12→qter) by array comparative genomic hybridization using uncultured amniocytesChih-Ping Chen, Shuan-Pei Lin, Yi-Ning Su, et al.
Prenatal Diagnosis|February 14, 2006
Molecular cytogenetic analysis of de novo dup(5)(q33.1q31.1) associated with abnormal perinatal findingsChih-Ping Chen, Shuan-Pei Lin, Schu-Rern Chern, et al.
Taiwanese Journal of Obstetrics & Gynecology|August 21, 2018
A 13-year-old girl with 18p deletion syndrome presenting Turner syndrome-like clinical features of short stature, short webbed neck, low posterior hair line, puffy eyelids and increased carrying angle of the elbowsChih-Ping Chen, Shuan-Pei Lin, Schu-Rern Chern, et al.
Prenatal Diagnosis|February 16, 2005
Perinatal findings and molecular cytogenetic analysis of de novo partial trisomy 16q (16q22.1-->qter) and partial monosomy 20q (20q13.3-->qter)Chih-Ping Chen, Shuan-Pei Lin, Chyi-Chyang Lin, et al.
Pageof 29

Showing results (141-150 of 281) with videos related to

Sort By:
Pageof 29
Gene|April 13, 2013
6p21.2-p12.3 deletion detected by aCGH in an 8-year-old girl with cleidocranial dysplasia and developmental delayChih-Ping Chen, Shuan-Pei Lin, Yu-Peng Liu, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|May 20, 2008
Genetic analysis of mucopolysaccharidosis type VI in Taiwanese patientsWei-De Lin, Shuan-Pei Lin, Chung-Hsing Wang, 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 disabilityChih-Ping Chen, Shuan-Pei Lin, Schu-Rern Chern, et al.
Taiwanese Journal of Obstetrics & Gynecology|April 29, 2014
Interphase FISH on uncultured amniocytes at repeat amniocentesis for rapid diagnosis of true mosaicism in a case of level II mosaicism involving trisomy 21 in a single colony from an in situ culture of amniocytesChih-Ping Chen, Pu-Tsui Wang, Shuan-Pei Lin, et al.
European Journal of Medical Genetics|June 15, 2010
A de novo 7.9 Mb deletion in 22q13.2→qter in a boy with autistic features, epilepsy, developmental delay, atopic dermatitis and abnormal immunological findingsChih-Ping Chen, Shuan-Pei Lin, Schu-Rern Chern, et al.
Journal of Human Genetics|July 16, 2010
Mutation spectrum of MMACHC in Chinese patients with combined methylmalonic aciduria and homocystinuriaMei-Ying Liu, Yan-Ling Yang, Ying-Chen Chang, et al.
Taiwanese Journal of Obstetrics & Gynecology|April 10, 2012
Rapid aneuploidy diagnosis of partial trisomy 7q (7q34→qter) and partial monosomy 10q (10q26.12→qter) by array comparative genomic hybridization using uncultured amniocytesChih-Ping Chen, Shuan-Pei Lin, Yi-Ning Su, et al.
Prenatal Diagnosis|February 14, 2006
Molecular cytogenetic analysis of de novo dup(5)(q33.1q31.1) associated with abnormal perinatal findingsChih-Ping Chen, Shuan-Pei Lin, Schu-Rern Chern, et al.
Taiwanese Journal of Obstetrics & Gynecology|August 21, 2018
A 13-year-old girl with 18p deletion syndrome presenting Turner syndrome-like clinical features of short stature, short webbed neck, low posterior hair line, puffy eyelids and increased carrying angle of the elbowsChih-Ping Chen, Shuan-Pei Lin, Schu-Rern Chern, et al.
Prenatal Diagnosis|February 16, 2005
Perinatal findings and molecular cytogenetic analysis of de novo partial trisomy 16q (16q22.1-->qter) and partial monosomy 20q (20q13.3-->qter)Chih-Ping Chen, Shuan-Pei Lin, Chyi-Chyang Lin, et al.
Pageof 29