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

J T Pang

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

Pageof 1
Sort By:
European Journal of Cancer (Oxford, England : 1990)|January 1, 1994
Multiple endocrine neoplasia type 1 (MEN1)J T Pang, R V Thakker
Human Genetics|May 1, 1997
Exclusion of ZFM1 as a candidate gene for multiple endocrine neoplasia type 1 (MEN1)S E Lloyd, J T Pang, S H Pearce, et al.
The Journal of Clinical Investigation|June 1, 1993
Mapping the gene causing X-linked recessive nephrolithiasis to Xp11.22 by linkage studiesS J Scheinman, M A Pook, C Wooding, et al.
Human Genetics|August 1, 1995
Linkage studies in a kindred from Oklahoma, with familial benign (hypocalciuric) hypercalcaemia (FBH) and developmental elevations in serum parathyroid hormone levels, indicate a third locus for FBHD Trump, M P Whyte, C Wooding, et al.
Henry Ford Hospital Medical Journal|January 1, 1992
Molecular genetic mapping of the multiple endocrine neoplasia type 1 locusJ T Pang, M A Pook, J H Eubanks, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|August 1, 1997
Linkage studies of a Missouri kindred with autosomal dominant spondyloepimetaphyseal dysplasia (SEMD) indicate genetic heterogeneityJ M Gertner, M P Whyte, P H Dixon, et al.
Journal of Medical Genetics|August 1, 1997
Localisation of a gene causing endocrine neoplasia to a 4 cM region on chromosome 1p35-p36C Williamson, A A Pannett, J T Pang, et al.
Annals of Human Genetics|January 1, 1993
Linkage analysis of 7 polymorphic markers at chromosome 11p11.2-11q13 in 27 multiple endocrine neoplasia type 1 familiesR V Thakker, C Wooding, J T Pang, et al.
Human Genetics|June 1, 1996
Genetic mapping studies of 40 loci and 23 cosmids in chromosome 11p13-11q13, and exclusion of mu-calpain as the multiple endocrine neoplasia type 1 geneJ T Pang, S E Lloyd, C Wooding, et al.
QJM : Monthly Journal of the Association of Physicians|September 1, 1996
Clinical studies of multiple endocrine neoplasia type 1 (MEN1)D Trump, B Farren, C Wooding, et al.
Pageof 1

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

Sort By:
Pageof 1
European Journal of Cancer (Oxford, England : 1990)|January 1, 1994
Multiple endocrine neoplasia type 1 (MEN1)J T Pang, R V Thakker
Human Genetics|May 1, 1997
Exclusion of ZFM1 as a candidate gene for multiple endocrine neoplasia type 1 (MEN1)S E Lloyd, J T Pang, S H Pearce, et al.
The Journal of Clinical Investigation|June 1, 1993
Mapping the gene causing X-linked recessive nephrolithiasis to Xp11.22 by linkage studiesS J Scheinman, M A Pook, C Wooding, et al.
Human Genetics|August 1, 1995
Linkage studies in a kindred from Oklahoma, with familial benign (hypocalciuric) hypercalcaemia (FBH) and developmental elevations in serum parathyroid hormone levels, indicate a third locus for FBHD Trump, M P Whyte, C Wooding, et al.
Henry Ford Hospital Medical Journal|January 1, 1992
Molecular genetic mapping of the multiple endocrine neoplasia type 1 locusJ T Pang, M A Pook, J H Eubanks, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|August 1, 1997
Linkage studies of a Missouri kindred with autosomal dominant spondyloepimetaphyseal dysplasia (SEMD) indicate genetic heterogeneityJ M Gertner, M P Whyte, P H Dixon, et al.
Journal of Medical Genetics|August 1, 1997
Localisation of a gene causing endocrine neoplasia to a 4 cM region on chromosome 1p35-p36C Williamson, A A Pannett, J T Pang, et al.
Annals of Human Genetics|January 1, 1993
Linkage analysis of 7 polymorphic markers at chromosome 11p11.2-11q13 in 27 multiple endocrine neoplasia type 1 familiesR V Thakker, C Wooding, J T Pang, et al.
Human Genetics|June 1, 1996
Genetic mapping studies of 40 loci and 23 cosmids in chromosome 11p13-11q13, and exclusion of mu-calpain as the multiple endocrine neoplasia type 1 geneJ T Pang, S E Lloyd, C Wooding, et al.
QJM : Monthly Journal of the Association of Physicians|September 1, 1996
Clinical studies of multiple endocrine neoplasia type 1 (MEN1)D Trump, B Farren, C Wooding, et al.
Pageof 1