Search research articles
Contact Us
Filters
Showing results (191-200 of 202) with videos related to
Page
of 21
Sort By:
Human Genetics
|
March 1, 1989
Study of a family with a fragile site of the X chromosome at Xq27-28 without mental retardation
M A Voelckel, N Philip, C Piquet, et al.
Genomics
|
November 1, 1989
CpG dinucleotides are mutation hot spots in phenylketonuria
V Abadie, S Lyonnet, N Maurin, et al.
Chirurgie Pediatrique
|
January 1, 1981
[Deformities of the lumbosacral spine and their visceral complications (myelomeningoceles excepted). Symposium of the French Society for Pediatric Surgery, 21-22 May 1981]
M Carcassonne, M Bergoin, M Choux, et al.
American Journal of Human Genetics
|
March 1, 1990
Slot blot method for the quantification of DNA sequences and mapping of chromosome rearrangements: application to chromosome 21
J L Blouin, Z Rahmani, Z Chettouh, et al.
Medecine Tropicale : Revue Du Corps De Sante Colonial
|
January 13, 2012
[Study of treatment adherence by patients living with HIV in 2009 at the outpatient care and treatment center of Brazzaville, Congo]
N Faure, M Diafouka, P Nzounza, et al.
Human Genetics
|
January 1, 1985
Linkage studies of X-linked mental retardation: high frequency of recombination in the telomeric region of the human X chromosome (fragile site/linkage/recombination/X chromosome)
K E Davies, M G Mattei, J F Mattei, et al.
European Journal of Human Genetics : EJHG
|
April 10, 1999
Phenotype-genotype correlation in 20 deletion and 20 non-deletion Angelman syndrome patients
A Moncla, P Malzac, M A Voelckel, et al.
Sante (Montrouge, France)
|
February 4, 2009
[Ten years of commitment to persons living with HIV-AIDS: evaluation of the management in three ambulatory treatment centers of the French Red Cross in Africa]
C Mouala, Y Madec, G Adam, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
August 1, 1989
Critical role of the D21S55 region on chromosome 21 in the pathogenesis of Down syndrome
Z Rahmani, J L Blouin, N Creau-Goldberg, et al.
Oncogene
|
January 1, 1990
Chromosomal localization of the three members of the jun proto-oncogene family in mouse and man
M G Mattei, D Simon-Chazottes, S Hirai, et al.
Page
of 21
Search research articles
Search
Showing results (191-200 of 202) with videos related to
Sort By:
Page
of 21
Human Genetics
|
March 1, 1989
Study of a family with a fragile site of the X chromosome at Xq27-28 without mental retardation
M A Voelckel, N Philip, C Piquet, et al.
Genomics
|
November 1, 1989
CpG dinucleotides are mutation hot spots in phenylketonuria
V Abadie, S Lyonnet, N Maurin, et al.
Chirurgie Pediatrique
|
January 1, 1981
[Deformities of the lumbosacral spine and their visceral complications (myelomeningoceles excepted). Symposium of the French Society for Pediatric Surgery, 21-22 May 1981]
M Carcassonne, M Bergoin, M Choux, et al.
American Journal of Human Genetics
|
March 1, 1990
Slot blot method for the quantification of DNA sequences and mapping of chromosome rearrangements: application to chromosome 21
J L Blouin, Z Rahmani, Z Chettouh, et al.
Medecine Tropicale : Revue Du Corps De Sante Colonial
|
January 13, 2012
[Study of treatment adherence by patients living with HIV in 2009 at the outpatient care and treatment center of Brazzaville, Congo]
N Faure, M Diafouka, P Nzounza, et al.
Human Genetics
|
January 1, 1985
Linkage studies of X-linked mental retardation: high frequency of recombination in the telomeric region of the human X chromosome (fragile site/linkage/recombination/X chromosome)
K E Davies, M G Mattei, J F Mattei, et al.
European Journal of Human Genetics : EJHG
|
April 10, 1999
Phenotype-genotype correlation in 20 deletion and 20 non-deletion Angelman syndrome patients
A Moncla, P Malzac, M A Voelckel, et al.
Sante (Montrouge, France)
|
February 4, 2009
[Ten years of commitment to persons living with HIV-AIDS: evaluation of the management in three ambulatory treatment centers of the French Red Cross in Africa]
C Mouala, Y Madec, G Adam, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
August 1, 1989
Critical role of the D21S55 region on chromosome 21 in the pathogenesis of Down syndrome
Z Rahmani, J L Blouin, N Creau-Goldberg, et al.
Oncogene
|
January 1, 1990
Chromosomal localization of the three members of the jun proto-oncogene family in mouse and man
M G Mattei, D Simon-Chazottes, S Hirai, et al.
Page
of 21