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

W Jan

Showing results (51-60 of 64) with videos related to

Pageof 7
Sort By:
Prenatal Diagnosis|June 1, 1996
Ultrasound-guided fluid aspiration and prenatal diagnosis of duplicated hydrometrocolpos with uterus didelphys and septate vaginaC P Chen, F F Liu, S W Jan, et al.
Clinical and Experimental Rheumatology|July 28, 2006
Coeliac artery stenosis and antiphospholipid (Hughes) syndrome/antiphospholipid anti-bodiesS R Sangle, W Jan, I S Lau, et al.
American Journal of Perinatology|August 1, 1996
Prenatal diagnosis and perinatal aspects of abdominal wall defectsC P Chen, F F Liu, S W Jan, et al.
American Journal of Perinatology|May 1, 1997
Perinatal features of omphalocele-exstrophy-imperforate anus-spinal defects (OEIS complex) associated with large meningomyeloceles and severe limb defectsC P Chen, S L Shih, F F Liu, et al.
Clinical Radiology|October 13, 2021
Diagnostic analysis of baseline brain MRI features in infants with congenital cytomegalovirus infection: a simplified scoring systemC Kachramanoglou, W Jan, B Jones, et al.
Prenatal Diagnosis|July 1, 1997
Prenatal diagnosis of partial trisomy 12 and partial trisomy 21 due to a 3:1 segregation of maternal reciprocal translocation t(12;21) (p13.3;q21)C P Chen, C C Lin, C Y Chuang, et al.
Annals of the Rheumatic Diseases|September 16, 2003
Renal artery stenosis in the antiphospholipid (Hughes) syndrome and hypertensionS R Sangle, D P D'Cruz, W Jan, et al.
Drug Metabolism and Drug Interactions|September 12, 2002
Pharmacokinetics of fluvoxamine in relation to CYP2C19 phenotype and genotypeMichael W Jan, Troy L ZumBrunnen, Yusuf R Kazmi, et al.
Prenatal Diagnosis|June 1, 1997
Prenatal diagnosis of a deletion of 18q in a fetus associated with multiple-marker screen positive resultsC P Chen, S R Chern, F F Liu, et al.
The British Journal of Dermatology|February 1, 1997
Cutis marmorata telangiectatica congenita associated with an elevated maternal serum human chorionic gonadotrophin level and transitory isolated fetal ascitesC P Chen, H C Chen, F F Liu, et al.
Pageof 7

Showing results (51-60 of 64) with videos related to

Sort By:
Pageof 7
Prenatal Diagnosis|June 1, 1996
Ultrasound-guided fluid aspiration and prenatal diagnosis of duplicated hydrometrocolpos with uterus didelphys and septate vaginaC P Chen, F F Liu, S W Jan, et al.
Clinical and Experimental Rheumatology|July 28, 2006
Coeliac artery stenosis and antiphospholipid (Hughes) syndrome/antiphospholipid anti-bodiesS R Sangle, W Jan, I S Lau, et al.
American Journal of Perinatology|August 1, 1996
Prenatal diagnosis and perinatal aspects of abdominal wall defectsC P Chen, F F Liu, S W Jan, et al.
American Journal of Perinatology|May 1, 1997
Perinatal features of omphalocele-exstrophy-imperforate anus-spinal defects (OEIS complex) associated with large meningomyeloceles and severe limb defectsC P Chen, S L Shih, F F Liu, et al.
Clinical Radiology|October 13, 2021
Diagnostic analysis of baseline brain MRI features in infants with congenital cytomegalovirus infection: a simplified scoring systemC Kachramanoglou, W Jan, B Jones, et al.
Prenatal Diagnosis|July 1, 1997
Prenatal diagnosis of partial trisomy 12 and partial trisomy 21 due to a 3:1 segregation of maternal reciprocal translocation t(12;21) (p13.3;q21)C P Chen, C C Lin, C Y Chuang, et al.
Annals of the Rheumatic Diseases|September 16, 2003
Renal artery stenosis in the antiphospholipid (Hughes) syndrome and hypertensionS R Sangle, D P D'Cruz, W Jan, et al.
Drug Metabolism and Drug Interactions|September 12, 2002
Pharmacokinetics of fluvoxamine in relation to CYP2C19 phenotype and genotypeMichael W Jan, Troy L ZumBrunnen, Yusuf R Kazmi, et al.
Prenatal Diagnosis|June 1, 1997
Prenatal diagnosis of a deletion of 18q in a fetus associated with multiple-marker screen positive resultsC P Chen, S R Chern, F F Liu, et al.
The British Journal of Dermatology|February 1, 1997
Cutis marmorata telangiectatica congenita associated with an elevated maternal serum human chorionic gonadotrophin level and transitory isolated fetal ascitesC P Chen, H C Chen, F F Liu, et al.
Pageof 7