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

M Anvret

Showing results (51-60 of 138) with videos related to

Pageof 14
Sort By:
Acta Paediatrica (Oslo, Norway : 1992)|February 1, 1996
Diagnosis of the Prader-Willi syndrome by proving the absence of the unmethylated PW71 DNA fragmentA C Lindgren, U Grandell, E M Ritzén, et al.
Developmental Medicine and Child Neurology|December 1, 1995
Parental exposure to hydrocarbons in Prader-Willi syndromeA Akefeldt, M Anvret, U Grandell, et al.
Human Genetics|March 1, 1988
DNA linkage analysis of X-linked retinoschisisN Dahl, P Goonewardena, J Chotai, et al.
Human Genetics|October 6, 1998
Phenotypic variation in a family with mutations in two Hirschsprung-related genes (RET and endothelin receptor B)P J Svensson, M Anvret, M L Molander, et al.
Human Molecular Genetics|December 1, 1992
Dinucleotide repeat polymorphism in the promoter region of the human von Willebrand factor gene (vWF gene)Z P Zhang, L P Deng, M Blombäck, et al.
Neuromuscular Disorders : NMD|May 1, 1997
Variation of CTG-repeat number of the DMPK gene in muscle tissueT Ansved, L Edström, U Grandell, et al.
Clinical Genetics|October 1, 1988
Infantile autism, fragile (X) (q27.3) and RFLP analysis in an extended Swedish familyM Anvret, C Gillberg, J Wahlström, et al.
Human Genetics|March 1, 1991
Molecular analysis of 4p deletion associated with Wolf-Hirschhorn syndrome moving the "critical segment" towards the telomereM Anvret, M Nordenskjöld, L Stolpe, et al.
Human Molecular Genetics|April 1, 1992
Identification of a new nonsense mutation in the von Willebrand factor gene in patients with von Willebrand disease type IIIZ P Zhang, G Falk, M Blombäck, et al.
Lakartidningen|January 29, 1997
[A new mutation causes achondrodysplasia. A simple DNA analysis confirms the diagnosis]A Alderborn, M Anvret, K H Gustavson, et al.
Pageof 14

Showing results (51-60 of 138) with videos related to

Sort By:
Pageof 14
Acta Paediatrica (Oslo, Norway : 1992)|February 1, 1996
Diagnosis of the Prader-Willi syndrome by proving the absence of the unmethylated PW71 DNA fragmentA C Lindgren, U Grandell, E M Ritzén, et al.
Developmental Medicine and Child Neurology|December 1, 1995
Parental exposure to hydrocarbons in Prader-Willi syndromeA Akefeldt, M Anvret, U Grandell, et al.
Human Genetics|March 1, 1988
DNA linkage analysis of X-linked retinoschisisN Dahl, P Goonewardena, J Chotai, et al.
Human Genetics|October 6, 1998
Phenotypic variation in a family with mutations in two Hirschsprung-related genes (RET and endothelin receptor B)P J Svensson, M Anvret, M L Molander, et al.
Human Molecular Genetics|December 1, 1992
Dinucleotide repeat polymorphism in the promoter region of the human von Willebrand factor gene (vWF gene)Z P Zhang, L P Deng, M Blombäck, et al.
Neuromuscular Disorders : NMD|May 1, 1997
Variation of CTG-repeat number of the DMPK gene in muscle tissueT Ansved, L Edström, U Grandell, et al.
Clinical Genetics|October 1, 1988
Infantile autism, fragile (X) (q27.3) and RFLP analysis in an extended Swedish familyM Anvret, C Gillberg, J Wahlström, et al.
Human Genetics|March 1, 1991
Molecular analysis of 4p deletion associated with Wolf-Hirschhorn syndrome moving the "critical segment" towards the telomereM Anvret, M Nordenskjöld, L Stolpe, et al.
Human Molecular Genetics|April 1, 1992
Identification of a new nonsense mutation in the von Willebrand factor gene in patients with von Willebrand disease type IIIZ P Zhang, G Falk, M Blombäck, et al.
Lakartidningen|January 29, 1997
[A new mutation causes achondrodysplasia. A simple DNA analysis confirms the diagnosis]A Alderborn, M Anvret, K H Gustavson, et al.
Pageof 14