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

I D Krantz

Showing results (1-10 of 21) with videos related to

Pageof 3
Sort By:
Clinical Genetics|October 2, 2009
Cornelia de Lange syndrome, cohesin, and beyondJ Liu, I D Krantz
Journal of Medical Genetics|February 1, 1997
Alagille syndromeI D Krantz, D A Piccoli, N B Spinner
Current Opinion in Pediatrics|December 11, 1999
Clinical and molecular genetics of Alagille syndromeI D Krantz, D A Piccoli, N B Spinner
Human Genetics|January 12, 2001
Chromosomal localization, genomic characterization, and mapping to the Noonan syndrome critical region of the human Deltex (DTX1) geneL Lee, J Dowhanick-Morrissette, A Katz, et al.
Journal of Medical Genetics|December 20, 2003
Consequences of JAG1 mutationsB M Kamath, L Bason, D A Piccoli, et al.
American Journal of Medical Genetics|December 26, 2001
Dominant paternal transmission of Cornelia de Lange syndrome: a new case and review of 25 previously reported familial recurrencesK L Russell, J E Ming, K Patel, et al.
Human Mutation|January 4, 2001
Jagged1 mutations in alagille syndromeN B Spinner, R P Colliton, C Crosnier, et al.
Hepatology (Baltimore, Md.)|March 3, 1999
Features of Alagille syndrome in 92 patients: frequency and relation to prognosisK M Emerick, E B Rand, E Goldmuntz, et al.
Human Mutation|February 17, 2001
Mutation analysis of Jagged1 (JAG1) in Alagille syndrome patientsR P Colliton, L Bason, F M Lu, et al.
American Journal of Medical Genetics|September 13, 2000
Duplication of chromosome region 4q28.3-qter in monozygotic twins with discordant phenotypesL Celle, L Lee, N Rintoul, et al.
Pageof 3

Showing results (1-10 of 21) with videos related to

Sort By:
Pageof 3
Clinical Genetics|October 2, 2009
Cornelia de Lange syndrome, cohesin, and beyondJ Liu, I D Krantz
Journal of Medical Genetics|February 1, 1997
Alagille syndromeI D Krantz, D A Piccoli, N B Spinner
Current Opinion in Pediatrics|December 11, 1999
Clinical and molecular genetics of Alagille syndromeI D Krantz, D A Piccoli, N B Spinner
Human Genetics|January 12, 2001
Chromosomal localization, genomic characterization, and mapping to the Noonan syndrome critical region of the human Deltex (DTX1) geneL Lee, J Dowhanick-Morrissette, A Katz, et al.
Journal of Medical Genetics|December 20, 2003
Consequences of JAG1 mutationsB M Kamath, L Bason, D A Piccoli, et al.
American Journal of Medical Genetics|December 26, 2001
Dominant paternal transmission of Cornelia de Lange syndrome: a new case and review of 25 previously reported familial recurrencesK L Russell, J E Ming, K Patel, et al.
Human Mutation|January 4, 2001
Jagged1 mutations in alagille syndromeN B Spinner, R P Colliton, C Crosnier, et al.
Hepatology (Baltimore, Md.)|March 3, 1999
Features of Alagille syndrome in 92 patients: frequency and relation to prognosisK M Emerick, E B Rand, E Goldmuntz, et al.
Human Mutation|February 17, 2001
Mutation analysis of Jagged1 (JAG1) in Alagille syndrome patientsR P Colliton, L Bason, F M Lu, et al.
American Journal of Medical Genetics|September 13, 2000
Duplication of chromosome region 4q28.3-qter in monozygotic twins with discordant phenotypesL Celle, L Lee, N Rintoul, et al.
Pageof 3