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

B D Gelb

Showing results (51-60 of 76) with videos related to

Pageof 8
Sort By:
American Journal of Human Genetics|August 16, 2001
Novel TFAP2B mutations that cause Char syndrome provide a genotype-phenotype correlationF Zhao, C G Weismann, M Satoda, et al.
Cytogenetics and Cell Genetics|January 1, 1997
Characterization of a de novo unbalanced chromosome rearrangement by comparative genomic hybridization and fluorescence in situ hybridizationB Levy, I F Gershin, R J Desnick, et al.
American Journal of Human Genetics|March 3, 1999
Diaphyseal medullary stenosis with malignant fibrous histiocytoma: a hereditary bone dysplasia/cancer syndrome maps to 9p21-22J A Martignetti, R J Desnick, E Aliprandis, et al.
Calcified Tissue International|July 23, 2003
Cathepsin K deficiency in pycnodysostosis results in accumulation of non-digested phagocytosed collagen in fibroblastsV Everts, W S Hou, X Rialland, et al.
The Journal of Heart and Lung Transplantation : the Official Publication of the International Society for Heart Transplantation|November 11, 1991
Pseudoconduction of atrial flutter of a recipient atriumB D Gelb, S Denfield, R Friedman, et al.
Genomics|April 15, 1997
Structure and chromosomal assignment of the human cathepsin K geneB D Gelb, G P Shi, M Heller, et al.
American Journal of Medical Genetics|April 15, 1994
Leigh syndrome and hypertrophic cardiomyopathy in an infant with a mitochondrial DNA point mutation (T8993G)G M Pastores, F M Santorelli, S Shanske, et al.
The Journal of Allergy and Clinical Immunology|July 11, 2000
Genetics of peanut allergy: a twin studyS H Sicherer, T J Furlong, H H Maes, et al.
Catheterization and Cardiovascular Diagnosis|February 1, 1993
Transcatheter closure of residual atrial septal defect following cardiac transplantationM P O'Laughlin, J T Bricker, C E Mullins, et al.
American Journal of Human Genetics|June 13, 1998
Paternal uniparental disomy for chromosome 1 revealed by molecular analysis of a patient with pycnodysostosisB D Gelb, J P Willner, T M Dunn, et al.
Pageof 8

Showing results (51-60 of 76) with videos related to

Sort By:
Pageof 8
American Journal of Human Genetics|August 16, 2001
Novel TFAP2B mutations that cause Char syndrome provide a genotype-phenotype correlationF Zhao, C G Weismann, M Satoda, et al.
Cytogenetics and Cell Genetics|January 1, 1997
Characterization of a de novo unbalanced chromosome rearrangement by comparative genomic hybridization and fluorescence in situ hybridizationB Levy, I F Gershin, R J Desnick, et al.
American Journal of Human Genetics|March 3, 1999
Diaphyseal medullary stenosis with malignant fibrous histiocytoma: a hereditary bone dysplasia/cancer syndrome maps to 9p21-22J A Martignetti, R J Desnick, E Aliprandis, et al.
Calcified Tissue International|July 23, 2003
Cathepsin K deficiency in pycnodysostosis results in accumulation of non-digested phagocytosed collagen in fibroblastsV Everts, W S Hou, X Rialland, et al.
The Journal of Heart and Lung Transplantation : the Official Publication of the International Society for Heart Transplantation|November 11, 1991
Pseudoconduction of atrial flutter of a recipient atriumB D Gelb, S Denfield, R Friedman, et al.
Genomics|April 15, 1997
Structure and chromosomal assignment of the human cathepsin K geneB D Gelb, G P Shi, M Heller, et al.
American Journal of Medical Genetics|April 15, 1994
Leigh syndrome and hypertrophic cardiomyopathy in an infant with a mitochondrial DNA point mutation (T8993G)G M Pastores, F M Santorelli, S Shanske, et al.
The Journal of Allergy and Clinical Immunology|July 11, 2000
Genetics of peanut allergy: a twin studyS H Sicherer, T J Furlong, H H Maes, et al.
Catheterization and Cardiovascular Diagnosis|February 1, 1993
Transcatheter closure of residual atrial septal defect following cardiac transplantationM P O'Laughlin, J T Bricker, C E Mullins, et al.
American Journal of Human Genetics|June 13, 1998
Paternal uniparental disomy for chromosome 1 revealed by molecular analysis of a patient with pycnodysostosisB D Gelb, J P Willner, T M Dunn, et al.
Pageof 8