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Human Genetics
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February 1, 1986
A case of female hemophilia with a 46,XXr karyotype studied with X-chromosome DNA probes
S Gilgenkrantz, M E Briquel, J L Mandel, et al.
Cytogenetics and Cell Genetics
|
January 1, 1987
Report of the committee on the genetic constitution of the X and Y chromosomes
K E Davies, J L Mandel, J Weissenbach, et al.
Folia Microbiologica
|
January 1, 1979
Development of lymphatic and haemopoietic organs in germfree models
F Kovárù, R Stĕpánková, J Kruml, et al.
Human Molecular Genetics
|
November 1, 1992
Two hot spots of recombination in the DMD gene correlate with the deletion prone regions
C Oudet, A Hanauer, P Clemens, et al.
Cancer
|
November 7, 2000
Ovarian carcinoma diagnosis
B A Goff, L Mandel, H G Muntz, et al.
Cytogenetics and Cell Genetics
|
July 15, 2000
Assignment of NUFIP1 (nuclear FMRP interacting protein 1) gene to chromosome 13q14 and assignment of a pseudogene to chromosome 6q12
B Bardoni, S Giglio, A Schenck, et al.
Nucleic Acids Research
|
July 24, 1987
A PstI RFLP detected by probe cpX73 (DXS159) in Xq11-q12
B Arveiler, M H Hofker, A A Bergen, et al.
Genomics
|
August 1, 1991
Physical mapping of two loci (D9S5 and D9S15) tightly linked to Friedreich ataxia locus (FRDA) and identification of nearby CpG islands by pulse-field gel electrophoresis
R Fujita, A Hanauer, A Vincent, et al.
Advances in Experimental Medicine and Biology
|
June 14, 2001
Pathological mechanisms in polyglutamine expansion diseases
D Devys, G Yvert, A Lunkes, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
July 5, 2001
A highly conserved protein family interacting with the fragile X mental retardation protein (FMRP) and displaying selective interactions with FMRP-related proteins FXR1P and FXR2P
A Schenck, B Bardoni, A Moro, et al.
Page
of 46
Search research articles
Search
Showing results (201-210 of 451) with videos related to
Sort By:
Page
of 46
Human Genetics
|
February 1, 1986
A case of female hemophilia with a 46,XXr karyotype studied with X-chromosome DNA probes
S Gilgenkrantz, M E Briquel, J L Mandel, et al.
Cytogenetics and Cell Genetics
|
January 1, 1987
Report of the committee on the genetic constitution of the X and Y chromosomes
K E Davies, J L Mandel, J Weissenbach, et al.
Folia Microbiologica
|
January 1, 1979
Development of lymphatic and haemopoietic organs in germfree models
F Kovárù, R Stĕpánková, J Kruml, et al.
Human Molecular Genetics
|
November 1, 1992
Two hot spots of recombination in the DMD gene correlate with the deletion prone regions
C Oudet, A Hanauer, P Clemens, et al.
Cancer
|
November 7, 2000
Ovarian carcinoma diagnosis
B A Goff, L Mandel, H G Muntz, et al.
Cytogenetics and Cell Genetics
|
July 15, 2000
Assignment of NUFIP1 (nuclear FMRP interacting protein 1) gene to chromosome 13q14 and assignment of a pseudogene to chromosome 6q12
B Bardoni, S Giglio, A Schenck, et al.
Nucleic Acids Research
|
July 24, 1987
A PstI RFLP detected by probe cpX73 (DXS159) in Xq11-q12
B Arveiler, M H Hofker, A A Bergen, et al.
Genomics
|
August 1, 1991
Physical mapping of two loci (D9S5 and D9S15) tightly linked to Friedreich ataxia locus (FRDA) and identification of nearby CpG islands by pulse-field gel electrophoresis
R Fujita, A Hanauer, A Vincent, et al.
Advances in Experimental Medicine and Biology
|
June 14, 2001
Pathological mechanisms in polyglutamine expansion diseases
D Devys, G Yvert, A Lunkes, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
July 5, 2001
A highly conserved protein family interacting with the fragile X mental retardation protein (FMRP) and displaying selective interactions with FMRP-related proteins FXR1P and FXR2P
A Schenck, B Bardoni, A Moro, et al.
Page
of 46