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

K Zerres

Showing results (141-150 of 174) with videos related to

Pageof 18
Sort By:
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|September 23, 2008
[Distal spinal-muscular atrophy 1 (DSMA1 or SMARD1)]A M Kaindl, U-P Guenther, S Rudnik-Schöneborn, et al.
Neuropediatrics|July 13, 2004
Long-term observations of patients with infantile spinal muscular atrophy with respiratory distress type 1 (SMARD1)S Rudnik-Schöneborn, P Stolz, R Varon, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|November 1, 1995
Sequence analysis of the human hTg737 gene and its polymorphic sites in patients with autosomal recessive polycystic kidney diseaseL F Onuchic, J J Schrick, J Ma, et al.
Clinical Nephrology|May 31, 2002
Analysis of the genes SLC7A9 and SLC3A1 in unclassified cystinurics: mutation detection rates and association between variants in SLC7A9 and the diseaseC Schmidt, A Albers, J Tomiuk, et al.
Nature Genetics|July 1, 1994
Mapping of the gene for autosomal recessive polycystic kidney disease (ARPKD) to chromosome 6p21-cenK Zerres, G Mücher, L Bachner, et al.
American Journal of Nephrology|January 1, 1988
Late manifestation of autosomal-recessive polycystic kidney disease in two sistersH P Neumann, K Zerres, C L Fischer, et al.
European Journal of Human Genetics : EJHG|January 1, 1995
Mapping of the spinal muscular atrophy (SMA) gene to a 750-kb interval flanked by two new microsatellitesB Wirth, A el-Agwany, A Baasner, et al.
Nature Genetics|September 10, 1998
Identification of a candidate modifying gene for spinal muscular atrophy by comparative genomicsJ M Scharf, M G Endrizzi, A Wetter, et al.
Clinical Genetics|June 18, 2004
New options for prenatal diagnosis in autosomal recessive polycystic kidney disease by mutation analysis of the PKHD1 geneK Zerres, J Senderek, S Rudnik-Schöneborn, et al.
Human Genetics|November 1, 1987
Autosomal recessive and dominant forms of polycystic kidney disease are not allelicB Wirth, K Zerres, M Fischbach, et al.
Pageof 18

Showing results (141-150 of 174) with videos related to

Sort By:
Pageof 18
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|September 23, 2008
[Distal spinal-muscular atrophy 1 (DSMA1 or SMARD1)]A M Kaindl, U-P Guenther, S Rudnik-Schöneborn, et al.
Neuropediatrics|July 13, 2004
Long-term observations of patients with infantile spinal muscular atrophy with respiratory distress type 1 (SMARD1)S Rudnik-Schöneborn, P Stolz, R Varon, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|November 1, 1995
Sequence analysis of the human hTg737 gene and its polymorphic sites in patients with autosomal recessive polycystic kidney diseaseL F Onuchic, J J Schrick, J Ma, et al.
Clinical Nephrology|May 31, 2002
Analysis of the genes SLC7A9 and SLC3A1 in unclassified cystinurics: mutation detection rates and association between variants in SLC7A9 and the diseaseC Schmidt, A Albers, J Tomiuk, et al.
Nature Genetics|July 1, 1994
Mapping of the gene for autosomal recessive polycystic kidney disease (ARPKD) to chromosome 6p21-cenK Zerres, G Mücher, L Bachner, et al.
American Journal of Nephrology|January 1, 1988
Late manifestation of autosomal-recessive polycystic kidney disease in two sistersH P Neumann, K Zerres, C L Fischer, et al.
European Journal of Human Genetics : EJHG|January 1, 1995
Mapping of the spinal muscular atrophy (SMA) gene to a 750-kb interval flanked by two new microsatellitesB Wirth, A el-Agwany, A Baasner, et al.
Nature Genetics|September 10, 1998
Identification of a candidate modifying gene for spinal muscular atrophy by comparative genomicsJ M Scharf, M G Endrizzi, A Wetter, et al.
Clinical Genetics|June 18, 2004
New options for prenatal diagnosis in autosomal recessive polycystic kidney disease by mutation analysis of the PKHD1 geneK Zerres, J Senderek, S Rudnik-Schöneborn, et al.
Human Genetics|November 1, 1987
Autosomal recessive and dominant forms of polycystic kidney disease are not allelicB Wirth, K Zerres, M Fischbach, et al.
Pageof 18