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Human Genetics
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January 1, 1985
A new MspI restriction fragment length polymorphism in the hemophilia B locus
G Camerino, I Oberlé, D Drayna, et al.
Human Genetics
|
April 1, 1989
A new polymorphic marker very closely linked to DXS52 in the q28 region of the human X chromosome
A Vincent, C Kretz, I Oberlé, et al.
Biochimica Et Biophysica Acta
|
June 20, 1990
Avian kidney mitochondrial hemeprotein P-4501 alpha: isolation, characterization and NADPH-ferredoxin reductase-dependent activity
M L Mandel, S J Swartz, J G Ghazarian
Radiobiologia, Radiotherapia
|
January 1, 1980
[Results of combined therapy of malignant renal tumours (author's transl)]
S Mau, K H Riessbeck, L Mandel, et al.
Nature Genetics
|
May 1, 1993
Origin of the expansion mutation in myotonic dystrophy
G Imbert, C Kretz, K Johnson, et al.
Nucleic Acids Research
|
May 25, 1984
A DNA fragment from the human X chromosome short arm which detects a partially homologous sequence on the Y chromosomes long arm
M Koenig, G Camerino, R Heilig, et al.
Human Genetics
|
February 1, 1990
New informative polymorphism at the DXS304 locus, a close distal marker for the fragile X locus
F Rousseau, A Vincent, I Oberlé, et al.
Nucleic Acids Research
|
July 24, 1982
The ovalbumin gene family: complete sequence and structure of the Y gene
R Heilig, R Muraskowsky, C Kloepfer, et al.
Nucleic Acids Research
|
July 11, 1988
A PstI RFLP for the human retinoic acid receptor in 17q21
B Arveiler, M Petkovich, J L Mandel, et al.
Journal of Medical Genetics
|
December 1, 1991
Selection in blood cells from female carriers of the fragile X syndrome: inverse correlation between age and proportion of active X chromosomes carrying the full mutation
F Rousseau, D Heitz, I Oberlé, et al.
Page
of 46
Search research articles
Search
Showing results (161-170 of 451) with videos related to
Sort By:
Page
of 46
Human Genetics
|
January 1, 1985
A new MspI restriction fragment length polymorphism in the hemophilia B locus
G Camerino, I Oberlé, D Drayna, et al.
Human Genetics
|
April 1, 1989
A new polymorphic marker very closely linked to DXS52 in the q28 region of the human X chromosome
A Vincent, C Kretz, I Oberlé, et al.
Biochimica Et Biophysica Acta
|
June 20, 1990
Avian kidney mitochondrial hemeprotein P-4501 alpha: isolation, characterization and NADPH-ferredoxin reductase-dependent activity
M L Mandel, S J Swartz, J G Ghazarian
Radiobiologia, Radiotherapia
|
January 1, 1980
[Results of combined therapy of malignant renal tumours (author's transl)]
S Mau, K H Riessbeck, L Mandel, et al.
Nature Genetics
|
May 1, 1993
Origin of the expansion mutation in myotonic dystrophy
G Imbert, C Kretz, K Johnson, et al.
Nucleic Acids Research
|
May 25, 1984
A DNA fragment from the human X chromosome short arm which detects a partially homologous sequence on the Y chromosomes long arm
M Koenig, G Camerino, R Heilig, et al.
Human Genetics
|
February 1, 1990
New informative polymorphism at the DXS304 locus, a close distal marker for the fragile X locus
F Rousseau, A Vincent, I Oberlé, et al.
Nucleic Acids Research
|
July 24, 1982
The ovalbumin gene family: complete sequence and structure of the Y gene
R Heilig, R Muraskowsky, C Kloepfer, et al.
Nucleic Acids Research
|
July 11, 1988
A PstI RFLP for the human retinoic acid receptor in 17q21
B Arveiler, M Petkovich, J L Mandel, et al.
Journal of Medical Genetics
|
December 1, 1991
Selection in blood cells from female carriers of the fragile X syndrome: inverse correlation between age and proportion of active X chromosomes carrying the full mutation
F Rousseau, D Heitz, I Oberlé, et al.
Page
of 46