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 Wehnert

Showing results (21-30 of 45) with videos related to

Pageof 5
Sort By:
Human Mutation|January 1, 1994
Mutations of the iduronate-2-sulfatase (IDS) gene in patients with Hunter syndrome (mucopolysaccharidosis II)W Schröder, K Wulff, M Wehnert, et al.
Clinical Genetics|September 1, 1988
Haplotype analysis of classical and mild phenotype of phenylketonuria in the German Democratic RepublicF H Herrmann, K Wulff, M Wehnert, et al.
Folia Haematologica (Leipzig, Germany : 1928)|January 1, 1988
First experiences in application of RFLP analysis for carrier detection in preparation of prenatal diagnosis of hemophilia A in the GDRF H Herrmann, T Kruse, M Wehnert, et al.
Biomedica Biochimica Acta|January 1, 1983
[Detection of phenylalanine hydroxylase activity in leukocytes and fibroblasts]U Grimm, A Knapp, A Weber, et al.
Genomics|November 1, 1996
Isolation, mapping, and genomic structure of an X-linked gene for a subunit of human mitochondrial complex IO Zhuchenko, M Wehnert, J Bailey, et al.
Neurology|June 1, 1997
Further evidence supporting linkage of hereditary neuralgic amyotrophy to chromosome 17qM Wehnert, V Timmerman, P Spoelders, et al.
Clinical Neuropathology|February 24, 2010
X-linked Emery-Dreifuss muscular dystrophy with lamin A deficiency and IBM inclusionsA Fidzianska, I Niebrój-Dobosz, A Madej-Pilarczyk, et al.
Human Heredity|January 1, 1991
Evidence supporting tight linkage of X-linked Emery-Dreifuss muscular dystrophy to the factor VIII:C geneM Wehnert, G Machill, T Grimm, et al.
Prenatal Diagnosis|August 1, 1990
Prenatal diagnosis of haemophilia A by the polymerase chain reaction using the intragenic hind III polymorphismM Wehnert, E L Shukova, V L Surin, et al.
Genome Research|November 1, 1996
Long-range map of a 3.5-Mb region in Xp11.23-22 with a sequence-ready map from a 1.1-Mb gene-rich intervalD Schindelhauer, H Hellebrand, L Grimm, et al.
Pageof 5

Showing results (21-30 of 45) with videos related to

Sort By:
Pageof 5
Human Mutation|January 1, 1994
Mutations of the iduronate-2-sulfatase (IDS) gene in patients with Hunter syndrome (mucopolysaccharidosis II)W Schröder, K Wulff, M Wehnert, et al.
Clinical Genetics|September 1, 1988
Haplotype analysis of classical and mild phenotype of phenylketonuria in the German Democratic RepublicF H Herrmann, K Wulff, M Wehnert, et al.
Folia Haematologica (Leipzig, Germany : 1928)|January 1, 1988
First experiences in application of RFLP analysis for carrier detection in preparation of prenatal diagnosis of hemophilia A in the GDRF H Herrmann, T Kruse, M Wehnert, et al.
Biomedica Biochimica Acta|January 1, 1983
[Detection of phenylalanine hydroxylase activity in leukocytes and fibroblasts]U Grimm, A Knapp, A Weber, et al.
Genomics|November 1, 1996
Isolation, mapping, and genomic structure of an X-linked gene for a subunit of human mitochondrial complex IO Zhuchenko, M Wehnert, J Bailey, et al.
Neurology|June 1, 1997
Further evidence supporting linkage of hereditary neuralgic amyotrophy to chromosome 17qM Wehnert, V Timmerman, P Spoelders, et al.
Clinical Neuropathology|February 24, 2010
X-linked Emery-Dreifuss muscular dystrophy with lamin A deficiency and IBM inclusionsA Fidzianska, I Niebrój-Dobosz, A Madej-Pilarczyk, et al.
Human Heredity|January 1, 1991
Evidence supporting tight linkage of X-linked Emery-Dreifuss muscular dystrophy to the factor VIII:C geneM Wehnert, G Machill, T Grimm, et al.
Prenatal Diagnosis|August 1, 1990
Prenatal diagnosis of haemophilia A by the polymerase chain reaction using the intragenic hind III polymorphismM Wehnert, E L Shukova, V L Surin, et al.
Genome Research|November 1, 1996
Long-range map of a 3.5-Mb region in Xp11.23-22 with a sequence-ready map from a 1.1-Mb gene-rich intervalD Schindelhauer, H Hellebrand, L Grimm, et al.
Pageof 5