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

S Chatkupt

Showing results (11-20 of 19) with videos related to

Pageof 2
Sort By:
You have reached the last page of results.This site can display upto 19 results.
American Journal of Medical Genetics|November 6, 1995
Reduced fecundity in male ALS gene-carriersW G Johnson, P R Lucek, S Chatkupt, et al.
Muscle & Nerve|January 1, 1997
Dejerine-Sottas neuropathy in mother and son with same point mutation of PMP22 geneV V Ionasescu, C C Searby, R Ionasescu, et al.
Neurology|January 1, 1994
Study of genetics, epidemiology, and vitamin usage in familial spina bifida in the United States in the 1990sS Chatkupt, J H Skurnick, M Jaggi, et al.
American Journal of Medical Genetics|December 14, 1999
Distribution of alleles of the methylenetetrahydrofolate reductase (MTHFR) C677T gene polymorphism in familial spina bifidaW G Johnson, E S Stenroos, S C Heath, et al.
American Journal of Medical Genetics|August 1, 1994
Linkage analysis of a candidate locus (HLA) in autosomal dominant sacral defect with anterior meningoceleS Chatkupt, M C Speer, Y Ding, et al.
American Journal of Human Genetics|March 1, 1994
Paternal isodisomy for chromosome 5 in a child with spinal muscular atrophyL M Brzustowicz, B A Allitto, D Matseoane, et al.
Journal of Medical Genetics|August 1, 1996
PAX genes and human neural tube defects: an amino acid substitution in PAX1 in a patient with spina bifidaF A Hol, M P Geurds, S Chatkupt, et al.
Journal of Medical Genetics|March 1, 1995
Absence of linkage between familial neural tube defects and PAX3 geneS Chatkupt, F A Hol, Y Y Shugart, et al.
Neurology|June 20, 1998
Clinical manifestations of mitochondrial DNA depletionT H Vu, M Sciacco, K Tanji, et al.
Pageof 2

Showing results (11-20 of 19) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 19 results.
American Journal of Medical Genetics|November 6, 1995
Reduced fecundity in male ALS gene-carriersW G Johnson, P R Lucek, S Chatkupt, et al.
Muscle & Nerve|January 1, 1997
Dejerine-Sottas neuropathy in mother and son with same point mutation of PMP22 geneV V Ionasescu, C C Searby, R Ionasescu, et al.
Neurology|January 1, 1994
Study of genetics, epidemiology, and vitamin usage in familial spina bifida in the United States in the 1990sS Chatkupt, J H Skurnick, M Jaggi, et al.
American Journal of Medical Genetics|December 14, 1999
Distribution of alleles of the methylenetetrahydrofolate reductase (MTHFR) C677T gene polymorphism in familial spina bifidaW G Johnson, E S Stenroos, S C Heath, et al.
American Journal of Medical Genetics|August 1, 1994
Linkage analysis of a candidate locus (HLA) in autosomal dominant sacral defect with anterior meningoceleS Chatkupt, M C Speer, Y Ding, et al.
American Journal of Human Genetics|March 1, 1994
Paternal isodisomy for chromosome 5 in a child with spinal muscular atrophyL M Brzustowicz, B A Allitto, D Matseoane, et al.
Journal of Medical Genetics|August 1, 1996
PAX genes and human neural tube defects: an amino acid substitution in PAX1 in a patient with spina bifidaF A Hol, M P Geurds, S Chatkupt, et al.
Journal of Medical Genetics|March 1, 1995
Absence of linkage between familial neural tube defects and PAX3 geneS Chatkupt, F A Hol, Y Y Shugart, et al.
Neurology|June 20, 1998
Clinical manifestations of mitochondrial DNA depletionT H Vu, M Sciacco, K Tanji, et al.
Pageof 2