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

R B Parad

Showing results (1-10 of 16) with videos related to

Pageof 2
Sort By:
Journal of Medical Genetics|August 1, 1996
Heterogeneity of phenotype in two cystic fibrosis patients homozygous for the CFTR exon 11 mutation G551DR B Parad
Pediatrics|May 23, 1998
Buccal cell DNA mutation analysis for diagnosis of cystic fibrosis in newborns and infants inaccessible to sweat chloride measurementR B Parad
Radiology|June 1, 1992
Prevalence of cystic fibrosis in fetuses with dilated bowelJ A Estroff, R B Parad, B R Benacerraf
American Journal of Respiratory and Critical Care Medicine|June 3, 1999
Variable levels of normal RNA in different fetal organs carrying a cystic fibrosis transmembrane conductance regulator splicing mutationO Chiba-Falek, R B Parad, E Kerem, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|May 1, 1992
The natural history of isolated fetal hydrothoraxJ A Estoff, R B Parad, F D Frigoletto, et al.
Journal of Ultrasound in Medicine : Official Journal of the American Institute of Ultrasound in Medicine|May 1, 1994
Second trimester prenatal findings in duodenal and esophageal atresia without tracheoesophageal fistulaJ A Estroff, R B Parad, J C Share, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 1, 1990
Dysfunctional C1 inhibitor Ta: deletion of Lys-251 results in acquisition of an N-glycosylation siteR B Parad, J Kramer, R C Strunk, et al.
Infection and Immunity|August 24, 1999
Pulmonary outcome in cystic fibrosis is influenced primarily by mucoid Pseudomonas aeruginosa infection and immune status and only modestly by genotypeR B Parad, C J Gerard, D Zurakowski, et al.
Journal of Perinatology : Official Journal of the California Perinatal Association|February 20, 2009
Economic evaluation of recombinant human copper zinc superoxide dismutase administered at birth to premature infantsJ A McBride, R B Parad, J M Davis, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 21, 2001
Genetic counseling after implementation of statewide cystic fibrosis newborn screening: Two years' experience in one medical centerP G Wheeler, R Smith, H Dorkin, et al.
Pageof 2

Showing results (1-10 of 16) with videos related to

Sort By:
Pageof 2
Journal of Medical Genetics|August 1, 1996
Heterogeneity of phenotype in two cystic fibrosis patients homozygous for the CFTR exon 11 mutation G551DR B Parad
Pediatrics|May 23, 1998
Buccal cell DNA mutation analysis for diagnosis of cystic fibrosis in newborns and infants inaccessible to sweat chloride measurementR B Parad
Radiology|June 1, 1992
Prevalence of cystic fibrosis in fetuses with dilated bowelJ A Estroff, R B Parad, B R Benacerraf
American Journal of Respiratory and Critical Care Medicine|June 3, 1999
Variable levels of normal RNA in different fetal organs carrying a cystic fibrosis transmembrane conductance regulator splicing mutationO Chiba-Falek, R B Parad, E Kerem, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|May 1, 1992
The natural history of isolated fetal hydrothoraxJ A Estoff, R B Parad, F D Frigoletto, et al.
Journal of Ultrasound in Medicine : Official Journal of the American Institute of Ultrasound in Medicine|May 1, 1994
Second trimester prenatal findings in duodenal and esophageal atresia without tracheoesophageal fistulaJ A Estroff, R B Parad, J C Share, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 1, 1990
Dysfunctional C1 inhibitor Ta: deletion of Lys-251 results in acquisition of an N-glycosylation siteR B Parad, J Kramer, R C Strunk, et al.
Infection and Immunity|August 24, 1999
Pulmonary outcome in cystic fibrosis is influenced primarily by mucoid Pseudomonas aeruginosa infection and immune status and only modestly by genotypeR B Parad, C J Gerard, D Zurakowski, et al.
Journal of Perinatology : Official Journal of the California Perinatal Association|February 20, 2009
Economic evaluation of recombinant human copper zinc superoxide dismutase administered at birth to premature infantsJ A McBride, R B Parad, J M Davis, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 21, 2001
Genetic counseling after implementation of statewide cystic fibrosis newborn screening: Two years' experience in one medical centerP G Wheeler, R Smith, H Dorkin, et al.
Pageof 2