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

I Kennerknecht

Showing results (21-30 of 44) with videos related to

Pageof 5
Sort By:
Prenatal Diagnosis|April 1, 1993
A prospective cytogenetic study of third-trimester placentae in small-for-date but otherwise normal newbornsI Kennerknecht, S Krämer, D Grab, et al.
Clinical Genetics|May 22, 2001
Recurrent mutations in the COL1A2 gene in patients with osteogenesis imperfectaT Trummer, R Brenner, W Just, et al.
Molecular and Cellular Biology|April 1, 1997
Characterization of a novel protein kinase C response element in the glucagon geneU Fürstenau, M Schwaninger, R Blume, et al.
The British Journal of Psychiatry : the Journal of Mental Science|January 1, 1994
DIDMOAD (Wolfram) syndromeM Kellner, F Strian, K Fassbender, et al.
Human Genetics|April 1, 1992
Genotype mosaicism in fragile X fetal tissuesD Wöhrle, M C Hirst, I Kennerknecht, et al.
American Journal of Medical Genetics|January 11, 1996
X/autosome translocation in three generations ascertained through an infant with trisomy 16p due to failure of spreading of X-inactivationW Preis, G Barbi, S Liptay, et al.
Human Molecular Genetics|July 1, 1995
Heterogeneity of DM kinase repeat expansion in different fetal tissues and further expansion during cell proliferation in vitro: evidence for a casual involvement of methyl-directed DNA mismatch repair in triplet repeat stabilityD Wöhrle, I Kennerknecht, M Wolf, et al.
Journal of Medical Genetics|September 19, 2000
The gene for branchio-oculo-facial syndrome does not colocalize to the EYA1-4 genesL S Correa-Cerro, I Kennerknecht, W Just, et al.
Prenatal Diagnosis|August 1, 1991
Uncommon chromosomal mosaicism in chorionic villiI Kennerknecht, G Barbi, M Djalali, et al.
American Journal of Medical Genetics|April 5, 2000
Mirror-symmetric duplicated chromosome 21q with minor proximal deletion, and with neocentromere in a child without the classical Down syndrome phenotypeG Barbi, I Kennerknecht, G Wöhr, et al.
Pageof 5

Showing results (21-30 of 44) with videos related to

Sort By:
Pageof 5
Prenatal Diagnosis|April 1, 1993
A prospective cytogenetic study of third-trimester placentae in small-for-date but otherwise normal newbornsI Kennerknecht, S Krämer, D Grab, et al.
Clinical Genetics|May 22, 2001
Recurrent mutations in the COL1A2 gene in patients with osteogenesis imperfectaT Trummer, R Brenner, W Just, et al.
Molecular and Cellular Biology|April 1, 1997
Characterization of a novel protein kinase C response element in the glucagon geneU Fürstenau, M Schwaninger, R Blume, et al.
The British Journal of Psychiatry : the Journal of Mental Science|January 1, 1994
DIDMOAD (Wolfram) syndromeM Kellner, F Strian, K Fassbender, et al.
Human Genetics|April 1, 1992
Genotype mosaicism in fragile X fetal tissuesD Wöhrle, M C Hirst, I Kennerknecht, et al.
American Journal of Medical Genetics|January 11, 1996
X/autosome translocation in three generations ascertained through an infant with trisomy 16p due to failure of spreading of X-inactivationW Preis, G Barbi, S Liptay, et al.
Human Molecular Genetics|July 1, 1995
Heterogeneity of DM kinase repeat expansion in different fetal tissues and further expansion during cell proliferation in vitro: evidence for a casual involvement of methyl-directed DNA mismatch repair in triplet repeat stabilityD Wöhrle, I Kennerknecht, M Wolf, et al.
Journal of Medical Genetics|September 19, 2000
The gene for branchio-oculo-facial syndrome does not colocalize to the EYA1-4 genesL S Correa-Cerro, I Kennerknecht, W Just, et al.
Prenatal Diagnosis|August 1, 1991
Uncommon chromosomal mosaicism in chorionic villiI Kennerknecht, G Barbi, M Djalali, et al.
American Journal of Medical Genetics|April 5, 2000
Mirror-symmetric duplicated chromosome 21q with minor proximal deletion, and with neocentromere in a child without the classical Down syndrome phenotypeG Barbi, I Kennerknecht, G Wöhr, et al.
Pageof 5