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

P Nürnberg

Showing results (41-50 of 115) with videos related to

Pageof 12
Sort By:
EXS|January 1, 1993
Oligonucleotide fingerprinting of free-ranging and captive rhesus macaques from Cayo Santiago: paternity assignment and comparison of heterozygosityP Nürnberg, J D Berard, F Bercovitch, et al.
Tissue Antigens|January 25, 2005
New strategies for efficient typing of HLA class-II loci DQB1 and DRB1 by using PyrosequencingP Entz, M R Toliat, J Hampe, et al.
Electrophoresis|March 22, 2000
Analysis of the NF1 gene by temperature gradient gel electrophoresis reveals a high incidence of mutations in exon 4bM R Toliat, F Erdogan, A Gewies, et al.
Pediatric Hematology and Oncology|December 29, 2000
Childhood all blasts retain phenotypic and genotypic characteristics upon long-term serial passage in NOD/SCID miceA Borgmann, C Baldy, A von Stackelberg, et al.
Blood|May 15, 1994
Mutations in the pyruvate kinase L gene in patients with hereditary hemolytic anemiaC Lenzner, P Nürnberg, B J Thiele, et al.
Clinical Genetics|April 4, 2017
Genome-wide linkage and sequence analysis challenge CCDC66 as a human retinal dystrophy candidate gene and support a distinct NMNAT1-related fundus phenotypeA O Khan, B S Budde, P Nürnberg, et al.
Human Genetics|July 1, 1995
Two recurrent nonsense mutations and a 4 bp deletion in a quasi-symmetric element in exon 37 of the NF1 geneP N Robinson, A Böddrich, H Peters, et al.
HNO|February 18, 2004
[Phenotypic characterization of a DFNA6 family with low-frequency hearing loss]T Tóth, S Kupka, P Nürnberg, et al.
Human Genetics|September 1, 1989
RFLP-discordance within the human phenylalanine hydroxylase locusO Riess, A Michel, W Berger, et al.
Clinical Genetics|February 1, 1991
Routine applications of DNA fingerprinting with the oligonucleotide probe (CAC)5/(GTG)5H Neitzel, M Digweed, P Nürnberg, et al.
Pageof 12

Showing results (41-50 of 115) with videos related to

Sort By:
Pageof 12
EXS|January 1, 1993
Oligonucleotide fingerprinting of free-ranging and captive rhesus macaques from Cayo Santiago: paternity assignment and comparison of heterozygosityP Nürnberg, J D Berard, F Bercovitch, et al.
Tissue Antigens|January 25, 2005
New strategies for efficient typing of HLA class-II loci DQB1 and DRB1 by using PyrosequencingP Entz, M R Toliat, J Hampe, et al.
Electrophoresis|March 22, 2000
Analysis of the NF1 gene by temperature gradient gel electrophoresis reveals a high incidence of mutations in exon 4bM R Toliat, F Erdogan, A Gewies, et al.
Pediatric Hematology and Oncology|December 29, 2000
Childhood all blasts retain phenotypic and genotypic characteristics upon long-term serial passage in NOD/SCID miceA Borgmann, C Baldy, A von Stackelberg, et al.
Blood|May 15, 1994
Mutations in the pyruvate kinase L gene in patients with hereditary hemolytic anemiaC Lenzner, P Nürnberg, B J Thiele, et al.
Clinical Genetics|April 4, 2017
Genome-wide linkage and sequence analysis challenge CCDC66 as a human retinal dystrophy candidate gene and support a distinct NMNAT1-related fundus phenotypeA O Khan, B S Budde, P Nürnberg, et al.
Human Genetics|July 1, 1995
Two recurrent nonsense mutations and a 4 bp deletion in a quasi-symmetric element in exon 37 of the NF1 geneP N Robinson, A Böddrich, H Peters, et al.
HNO|February 18, 2004
[Phenotypic characterization of a DFNA6 family with low-frequency hearing loss]T Tóth, S Kupka, P Nürnberg, et al.
Human Genetics|September 1, 1989
RFLP-discordance within the human phenylalanine hydroxylase locusO Riess, A Michel, W Berger, et al.
Clinical Genetics|February 1, 1991
Routine applications of DNA fingerprinting with the oligonucleotide probe (CAC)5/(GTG)5H Neitzel, M Digweed, P Nürnberg, et al.
Pageof 12