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European Journal of Human Genetics : EJHG
|
January 15, 1999
Genetic linkage of Meleda disease to chromosome 8qter
J Fischer, B Bouadjar, R Heilig, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
October 1, 1990
Isolated dystrophin molecules as seen by electron microscopy
F Pons, N Augier, R Heilig, et al.
American Journal of Medical Genetics
|
May 1, 1988
Improved DNA markers for efficient analysis of fragile X families
R Heilig, I Oberlé, B Arveiler, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia
|
January 19, 2012
Natural history of platelet antibody formation against αIIbβ3 in a French cohort of Glanzmann thrombasthenia patients
M Fiore, N Firah, X Pillois, et al.
Nature
|
July 9, 1987
Localization of the region homologous to the Duchenne muscular dystrophy locus on the mouse X chromosome
R Heilig, C Lemaire, J L Mandel, et al.
Nucleic Acids Research
|
June 11, 1983
Isolation and characterization of cDNA clones for human skeletal muscle alpha actin
A Hanauer, M Levin, R Heilig, et al.
Zeitschrift Fur Naturforschung. C, Journal of Biosciences
|
May 1, 1991
Slit scan flow cytometry of isolated chromosomes following fluorescence hybridization: an approach of online screening for specific chromosomes and chromosome translocations
M Hausmann, G Dudin, J A Aten, et al.
American Journal of Human Genetics
|
April 1, 1990
Physical and genetic mapping of polymorphic loci in Xq28 (DXS15, DXS52, and DXS134): analysis of a cosmid clone and a yeast artificial chromosome
R Feil, G Palmieri, M d'Urso, et al.
The EMBO Journal
|
August 1, 1984
Actin-like sequences are present on human X and Y chromosomes
R Heilig, A Hanauer, K H Grzeschik, et al.
American Journal of Human Genetics
|
March 11, 2000
Characterization of the NPHP1 locus: mutational mechanism involved in deletions in familial juvenile nephronophthisis
S Saunier, J Calado, F Benessy, et al.
Page
of 7
Search research articles
Search
Showing results (31-40 of 67) with videos related to
Sort By:
Page
of 7
European Journal of Human Genetics : EJHG
|
January 15, 1999
Genetic linkage of Meleda disease to chromosome 8qter
J Fischer, B Bouadjar, R Heilig, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
October 1, 1990
Isolated dystrophin molecules as seen by electron microscopy
F Pons, N Augier, R Heilig, et al.
American Journal of Medical Genetics
|
May 1, 1988
Improved DNA markers for efficient analysis of fragile X families
R Heilig, I Oberlé, B Arveiler, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia
|
January 19, 2012
Natural history of platelet antibody formation against αIIbβ3 in a French cohort of Glanzmann thrombasthenia patients
M Fiore, N Firah, X Pillois, et al.
Nature
|
July 9, 1987
Localization of the region homologous to the Duchenne muscular dystrophy locus on the mouse X chromosome
R Heilig, C Lemaire, J L Mandel, et al.
Nucleic Acids Research
|
June 11, 1983
Isolation and characterization of cDNA clones for human skeletal muscle alpha actin
A Hanauer, M Levin, R Heilig, et al.
Zeitschrift Fur Naturforschung. C, Journal of Biosciences
|
May 1, 1991
Slit scan flow cytometry of isolated chromosomes following fluorescence hybridization: an approach of online screening for specific chromosomes and chromosome translocations
M Hausmann, G Dudin, J A Aten, et al.
American Journal of Human Genetics
|
April 1, 1990
Physical and genetic mapping of polymorphic loci in Xq28 (DXS15, DXS52, and DXS134): analysis of a cosmid clone and a yeast artificial chromosome
R Feil, G Palmieri, M d'Urso, et al.
The EMBO Journal
|
August 1, 1984
Actin-like sequences are present on human X and Y chromosomes
R Heilig, A Hanauer, K H Grzeschik, et al.
American Journal of Human Genetics
|
March 11, 2000
Characterization of the NPHP1 locus: mutational mechanism involved in deletions in familial juvenile nephronophthisis
S Saunier, J Calado, F Benessy, et al.
Page
of 7