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Human Molecular Genetics
|
August 1, 1992
Dinucleotide repeat polymorphism at the D21S65 locus
J Goto, F Tassone, S Demczuk, et al.
Human Molecular Genetics
|
October 1, 1993
Isolation of a zinc finger gene consistently deleted in DiGeorge syndrome
M Aubry, S Demczuk, C Desmaze, et al.
Polish Journal of Pathology : Official Journal of the Polish Society of Pathologists
|
August 15, 2014
Selected immunohistochemical features of conventional renal cell carcinomas coexpressing P53 and MDM2
M Hejnold, G Dyduch, M Białas, et al.
Genomics
|
September 1, 1993
Isolation and mapping of 45 NotI linking clones to chromosome 22
M Sanson, F Zhang, S Demczuk, et al.
Annales De Genetique
|
January 1, 1994
Molecular cytogenetic analysis of a series of 23 DiGeorge syndrome patients by fluorescence in situ hybridization
S Demczuk, C Desmaze, M Aikem, et al.
Biochemistry International
|
March 1, 1987
Limited effects of recombinant human and murine interleukin 1 and tumour necrosis factor on production of acute phase proteins by cultured rat hepatocytes
A Koj, A Kurdowska, D Magielska-Zero, et al.
Journal of Medical Genetics
|
March 21, 1998
Prenatal diagnosis by FISH of a 22q11 deletion in two families
M F Portnoï, N Joyé, M Gonzales, et al.
Human Molecular Genetics
|
April 1, 1995
Cloning of a balanced translocation breakpoint in the DiGeorge syndrome critical region and isolation of a novel potential adhesion receptor gene in its vicinity
S Demczuk, R Aledo, J Zucman, et al.
Human Genetics
|
February 1, 1996
Familial non-syndromic conotruncal defects are not associated with a 22q11 microdeletion
S Debrus, G Berger, A de Meeus, et al.
American Journal of Human Genetics
|
December 1, 1993
Physical mapping by FISH of the DiGeorge critical region (DGCR): involvement of the region in familial cases
C Desmaze, M Prieur, F Amblard, et al.
Page
of 4
Search research articles
Search
Showing results (21-30 of 34) with videos related to
Sort By:
Page
of 4
Human Molecular Genetics
|
August 1, 1992
Dinucleotide repeat polymorphism at the D21S65 locus
J Goto, F Tassone, S Demczuk, et al.
Human Molecular Genetics
|
October 1, 1993
Isolation of a zinc finger gene consistently deleted in DiGeorge syndrome
M Aubry, S Demczuk, C Desmaze, et al.
Polish Journal of Pathology : Official Journal of the Polish Society of Pathologists
|
August 15, 2014
Selected immunohistochemical features of conventional renal cell carcinomas coexpressing P53 and MDM2
M Hejnold, G Dyduch, M Białas, et al.
Genomics
|
September 1, 1993
Isolation and mapping of 45 NotI linking clones to chromosome 22
M Sanson, F Zhang, S Demczuk, et al.
Annales De Genetique
|
January 1, 1994
Molecular cytogenetic analysis of a series of 23 DiGeorge syndrome patients by fluorescence in situ hybridization
S Demczuk, C Desmaze, M Aikem, et al.
Biochemistry International
|
March 1, 1987
Limited effects of recombinant human and murine interleukin 1 and tumour necrosis factor on production of acute phase proteins by cultured rat hepatocytes
A Koj, A Kurdowska, D Magielska-Zero, et al.
Journal of Medical Genetics
|
March 21, 1998
Prenatal diagnosis by FISH of a 22q11 deletion in two families
M F Portnoï, N Joyé, M Gonzales, et al.
Human Molecular Genetics
|
April 1, 1995
Cloning of a balanced translocation breakpoint in the DiGeorge syndrome critical region and isolation of a novel potential adhesion receptor gene in its vicinity
S Demczuk, R Aledo, J Zucman, et al.
Human Genetics
|
February 1, 1996
Familial non-syndromic conotruncal defects are not associated with a 22q11 microdeletion
S Debrus, G Berger, A de Meeus, et al.
American Journal of Human Genetics
|
December 1, 1993
Physical mapping by FISH of the DiGeorge critical region (DGCR): involvement of the region in familial cases
C Desmaze, M Prieur, F Amblard, et al.
Page
of 4