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 B Petersen

Showing results (81-90 of 140) with videos related to

Pageof 14
Sort By:
American Journal of Medical Genetics. Part A|November 15, 2006
A report of pure 7p duplication syndrome and review of the literatureE Papadopoulou, S Sifakis, C Sarri, et al.
Genomics|March 1, 1991
A genetic linkage map of 27 markers on human chromosome 21M B Petersen, S A Slaugenhaupt, J G Lewis, et al.
Human Genetics|September 1, 1993
Cytogenetic, FISH and DNA studies in 11 individuals from a family with two siblings with dup(21q) Down syndromeO Bartsch, U König, M B Petersen, et al.
Genomics|November 1, 1991
Linkage mapping of highly informative DNA polymorphisms within the human interferon-alpha receptor gene on chromosome 21M G McInnis, G Lutfalla, S Slaugenhaupt, et al.
Clinical Genetics|August 1, 1993
Application of molecular and cytogenetic techniques to the detection of a de novo unbalanced t(11q;21q) in a patient previously diagnosed as having monosomy 21B Hertz, C A Brandt, M B Petersen, et al.
Clinical Genetics|July 1, 1997
A patient with Edwards syndrome caused by a rare pseudodicentric chromosome 18 of paternal originC H Gravholt, M Bugge, H Strømkjaer, et al.
Journal of Medical Genetics|July 1, 1997
A case of apparent trisomy 21 without the Down's syndrome phenotypeD Avramopoulos, I Kennerknecht, G Barbi, et al.
Clinical Genetics|January 24, 1998
Apolipoprotein E polymorphism in the Greek populationE Sklavounou, E Economou-Petersen, G Karadima, et al.
Genomics|November 1, 1992
Dinucleotide repeat (GT)n markers on chromosome 21A C Warren, M G McInnis, J Blaschak, et al.
Human Mutation|July 20, 2001
Detection of mutations in the COL4A5 gene by SSCP in X-linked Alport syndromeJ M Hertz, I Juncker, U Persson, et al.
Pageof 14

Showing results (81-90 of 140) with videos related to

Sort By:
Pageof 14
American Journal of Medical Genetics. Part A|November 15, 2006
A report of pure 7p duplication syndrome and review of the literatureE Papadopoulou, S Sifakis, C Sarri, et al.
Genomics|March 1, 1991
A genetic linkage map of 27 markers on human chromosome 21M B Petersen, S A Slaugenhaupt, J G Lewis, et al.
Human Genetics|September 1, 1993
Cytogenetic, FISH and DNA studies in 11 individuals from a family with two siblings with dup(21q) Down syndromeO Bartsch, U König, M B Petersen, et al.
Genomics|November 1, 1991
Linkage mapping of highly informative DNA polymorphisms within the human interferon-alpha receptor gene on chromosome 21M G McInnis, G Lutfalla, S Slaugenhaupt, et al.
Clinical Genetics|August 1, 1993
Application of molecular and cytogenetic techniques to the detection of a de novo unbalanced t(11q;21q) in a patient previously diagnosed as having monosomy 21B Hertz, C A Brandt, M B Petersen, et al.
Clinical Genetics|July 1, 1997
A patient with Edwards syndrome caused by a rare pseudodicentric chromosome 18 of paternal originC H Gravholt, M Bugge, H Strømkjaer, et al.
Journal of Medical Genetics|July 1, 1997
A case of apparent trisomy 21 without the Down's syndrome phenotypeD Avramopoulos, I Kennerknecht, G Barbi, et al.
Clinical Genetics|January 24, 1998
Apolipoprotein E polymorphism in the Greek populationE Sklavounou, E Economou-Petersen, G Karadima, et al.
Genomics|November 1, 1992
Dinucleotide repeat (GT)n markers on chromosome 21A C Warren, M G McInnis, J Blaschak, et al.
Human Mutation|July 20, 2001
Detection of mutations in the COL4A5 gene by SSCP in X-linked Alport syndromeJ M Hertz, I Juncker, U Persson, et al.
Pageof 14