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Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
January 14, 1999
[Persistent hyperinsulinemic hypoglycemia in the newborn and infants]
P de Lonlay-Debeney, J C Fournet, D Martin, et al.
Nucleic Acids Research
|
January 1, 1997
Marfan Database (second edition): software and database for the analysis of mutations in the human FBN1 gene
G Collod-Béroud, C Béroud, L Adès, et al.
European Journal of Human Genetics : EJHG
|
August 22, 2000
Autosomal dominant type IIa hypercholesterolemia: evaluation of the respective contributions of LDLR and APOB gene defects as well as a third major group of defects
B Saint-Jore, M Varret, C Dachet, et al.
Journal De La Societe De Biologie
|
December 7, 2000
[Prevention of renal carcinoma: the nutri-genetic approach]
C Junien, J M Dupret, C Gallou, et al.
Placenta
|
July 10, 2010
Placental BDNF/TrkB signaling system is modulated by fetal growth disturbances in rat and human
S Mayeur, M Silhol, E Moitrot, et al.
The Journal of Clinical Investigation
|
August 15, 1997
Somatic deletion of the imprinted 11p15 region in sporadic persistent hyperinsulinemic hypoglycemia of infancy is specific of focal adenomatous hyperplasia and endorses partial pancreatectomy
P de Lonlay, J C Fournet, J Rahier, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
November 1, 1982
Human type I procollagen genes are located on different chromosomes
C Huerre, C Junien, D Weil, et al.
Nucleic Acids Research
|
February 21, 1998
LDLR Database (second edition): new additions to the database and the software, and results of the first molecular analysis
M Varret, J P Rabés, R Thiart, et al.
Endocrine Reviews
|
October 26, 2010
Child health, developmental plasticity, and epigenetic programming
Z Hochberg, R Feil, M Constancia, et al.
Nucleic Acids Research
|
February 21, 1998
Marfan Database (third edition): new mutations and new routines for the software
G Collod-Béroud, C Béroud, L Ades, et al.
Page
of 29
Search research articles
Search
Showing results (271-280 of 284) with videos related to
Sort By:
Page
of 29
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
January 14, 1999
[Persistent hyperinsulinemic hypoglycemia in the newborn and infants]
P de Lonlay-Debeney, J C Fournet, D Martin, et al.
Nucleic Acids Research
|
January 1, 1997
Marfan Database (second edition): software and database for the analysis of mutations in the human FBN1 gene
G Collod-Béroud, C Béroud, L Adès, et al.
European Journal of Human Genetics : EJHG
|
August 22, 2000
Autosomal dominant type IIa hypercholesterolemia: evaluation of the respective contributions of LDLR and APOB gene defects as well as a third major group of defects
B Saint-Jore, M Varret, C Dachet, et al.
Journal De La Societe De Biologie
|
December 7, 2000
[Prevention of renal carcinoma: the nutri-genetic approach]
C Junien, J M Dupret, C Gallou, et al.
Placenta
|
July 10, 2010
Placental BDNF/TrkB signaling system is modulated by fetal growth disturbances in rat and human
S Mayeur, M Silhol, E Moitrot, et al.
The Journal of Clinical Investigation
|
August 15, 1997
Somatic deletion of the imprinted 11p15 region in sporadic persistent hyperinsulinemic hypoglycemia of infancy is specific of focal adenomatous hyperplasia and endorses partial pancreatectomy
P de Lonlay, J C Fournet, J Rahier, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
November 1, 1982
Human type I procollagen genes are located on different chromosomes
C Huerre, C Junien, D Weil, et al.
Nucleic Acids Research
|
February 21, 1998
LDLR Database (second edition): new additions to the database and the software, and results of the first molecular analysis
M Varret, J P Rabés, R Thiart, et al.
Endocrine Reviews
|
October 26, 2010
Child health, developmental plasticity, and epigenetic programming
Z Hochberg, R Feil, M Constancia, et al.
Nucleic Acids Research
|
February 21, 1998
Marfan Database (third edition): new mutations and new routines for the software
G Collod-Béroud, C Béroud, L Ades, et al.
Page
of 29