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Gene
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July 18, 1997
Human growth hormone receptor: cloning and expression of the full-length complementary DNA after site-directed inactivation of a cryptic bacterial promoter
E Bieth, C Cahoreau, S Cholin, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
March 10, 2001
[CFTR gene analyis in 207 patients with cystic fibrosis in southwest France: high frequency of N1303K and 1811+1.6bA>G mutations]
S Federici, A Iron, M P Reboul, et al.
Biology of the Neonate
|
June 9, 1998
Growth hormone, insulin-like growth factor-I and insulin-like growth factor binding protein-3 are regulated differently in small-for-gestational-age and appropriate-for-gestational-age neonates
A Cance-Rouzaud, S Laborie, E Bieth, et al.
Neurology
|
July 1, 2009
Re: CDKL5 mutations in boys with severe encephalopathy and early-onset intractable epilepsy
Y Fichou, E Bieth, N Bahi-Buisson, et al.
Growth Hormone & IGF Research : Official Journal of the Growth Hormone Research Society and the International IGF Research Society
|
September 13, 2000
Heterozygous mutation in the WSXWS equivalaent motif of the growth hormone receptor in a child with poor response to growth hormone therapy
M T Tauber, V Porra, F Dastot, et al.
American Journal of Medical Genetics. Part A
|
July 21, 2004
Molecular characterization of a cryptic 2q37 deletion in a patient with Albright hereditary osteodystrophy-like phenotype
N Chassaing, P De Mas, M Tauber, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
March 17, 2020
Genetic counseling for cystic fibrosis: A basic model with new challenges
E Bieth, J Nectoux, A Girardet, et al.
Journal of Medical Genetics
|
April 16, 2002
Molecular characterisation of a ring chromosome 22 in a patient with severe language delay: a contribution to the refinement of the subtelomeric 22q deletion syndrome
P De Mas, N Chassaing, Y Chaix, et al.
Biochimie
|
January 1, 1996
Expression of a recombinant human growth hormone binding protein in baculovirus/insect cell system
S Cholin, E Bieth, C Molinas, et al.
Hormone Research
|
March 17, 2001
Evaluation of cutaneous modifications in seventy-seven growth hormone-deficient children
F Conte, S Diridollou, B Jouret, et al.
Page
of 4
Search research articles
Search
Showing results (11-20 of 36) with videos related to
Sort By:
Page
of 4
Gene
|
July 18, 1997
Human growth hormone receptor: cloning and expression of the full-length complementary DNA after site-directed inactivation of a cryptic bacterial promoter
E Bieth, C Cahoreau, S Cholin, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
March 10, 2001
[CFTR gene analyis in 207 patients with cystic fibrosis in southwest France: high frequency of N1303K and 1811+1.6bA>G mutations]
S Federici, A Iron, M P Reboul, et al.
Biology of the Neonate
|
June 9, 1998
Growth hormone, insulin-like growth factor-I and insulin-like growth factor binding protein-3 are regulated differently in small-for-gestational-age and appropriate-for-gestational-age neonates
A Cance-Rouzaud, S Laborie, E Bieth, et al.
Neurology
|
July 1, 2009
Re: CDKL5 mutations in boys with severe encephalopathy and early-onset intractable epilepsy
Y Fichou, E Bieth, N Bahi-Buisson, et al.
Growth Hormone & IGF Research : Official Journal of the Growth Hormone Research Society and the International IGF Research Society
|
September 13, 2000
Heterozygous mutation in the WSXWS equivalaent motif of the growth hormone receptor in a child with poor response to growth hormone therapy
M T Tauber, V Porra, F Dastot, et al.
American Journal of Medical Genetics. Part A
|
July 21, 2004
Molecular characterization of a cryptic 2q37 deletion in a patient with Albright hereditary osteodystrophy-like phenotype
N Chassaing, P De Mas, M Tauber, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
March 17, 2020
Genetic counseling for cystic fibrosis: A basic model with new challenges
E Bieth, J Nectoux, A Girardet, et al.
Journal of Medical Genetics
|
April 16, 2002
Molecular characterisation of a ring chromosome 22 in a patient with severe language delay: a contribution to the refinement of the subtelomeric 22q deletion syndrome
P De Mas, N Chassaing, Y Chaix, et al.
Biochimie
|
January 1, 1996
Expression of a recombinant human growth hormone binding protein in baculovirus/insect cell system
S Cholin, E Bieth, C Molinas, et al.
Hormone Research
|
March 17, 2001
Evaluation of cutaneous modifications in seventy-seven growth hormone-deficient children
F Conte, S Diridollou, B Jouret, et al.
Page
of 4