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Annales D'Endocrinologie
|
July 1, 2005
[The Paris experience in preimplantation genetic diagnosis: evaluation after the first births]
N Frydman, S Romana, P Ray, et al.
Human Genetics
|
August 14, 2001
Partial maternal heterodisomy of chromosome 17q25 in a case of severe mental retardation
M Rio, C Ozilou, V Cormier-Daire, et al.
Organic Letters
|
January 27, 2006
Synthesis of 3,6-diaminophthalimides for ureidophthalimide-based foldamers
Renatus W Sinkeldam, Michel H C J van Houtem, Guy Koeckelberghs, et al.
Hepatology (Baltimore, Md.)
|
August 29, 2000
JAGGED1 gene expression during human embryogenesis elucidates the wide phenotypic spectrum of Alagille syndrome
C Crosnier, T Attié-Bitach, F Encha-Razavi, et al.
American Journal of Medical Genetics
|
April 15, 2000
Apparent Sotos syndrome (cerebral gigantism) in a child with trisomy 20p11.2-p12.1 mosaicism
L Faivre, G Viot, M Prieur, et al.
American Journal of Medical Genetics
|
December 26, 2001
Chromosome 10p11.2-p12.2 duplication: report of a patient and review of the literature
A Mégarbané, P Gosset, N Souraty, et al.
Mechanisms of Development
|
April 27, 2000
Regional and cellular specificity of the expression of TPRD, the tetratricopeptide Down syndrome gene, during human embryonic development
M Rachidi, C Lopes, S Gassanova, et al.
The Journal of Organic Chemistry
|
September 6, 1996
Hydrogen-Bonded Complexes of Diaminopyridines and Diaminotriazines: Opposite Effect of Acylation on Complex Stabilities
Felix H. Beijer, Rint P. Sijbesma, Jef A. J. M. Vekemans, et al.
American Journal of Human Genetics
|
April 17, 1999
Recurrent Williams-Beuren syndrome in a sibship suggestive of maternal germ-line mosaicism
A Kara-Mostefa, O Raoul, S Lyonnet, et al.
American Journal of Medical Genetics
|
March 13, 1995
Upper limb malformations in DiGeorge syndrome
V Cormier-Daire, L Iserin, D Théophile, et al.
Page
of 29
Search research articles
Search
Showing results (181-190 of 289) with videos related to
Sort By:
Page
of 29
Annales D'Endocrinologie
|
July 1, 2005
[The Paris experience in preimplantation genetic diagnosis: evaluation after the first births]
N Frydman, S Romana, P Ray, et al.
Human Genetics
|
August 14, 2001
Partial maternal heterodisomy of chromosome 17q25 in a case of severe mental retardation
M Rio, C Ozilou, V Cormier-Daire, et al.
Organic Letters
|
January 27, 2006
Synthesis of 3,6-diaminophthalimides for ureidophthalimide-based foldamers
Renatus W Sinkeldam, Michel H C J van Houtem, Guy Koeckelberghs, et al.
Hepatology (Baltimore, Md.)
|
August 29, 2000
JAGGED1 gene expression during human embryogenesis elucidates the wide phenotypic spectrum of Alagille syndrome
C Crosnier, T Attié-Bitach, F Encha-Razavi, et al.
American Journal of Medical Genetics
|
April 15, 2000
Apparent Sotos syndrome (cerebral gigantism) in a child with trisomy 20p11.2-p12.1 mosaicism
L Faivre, G Viot, M Prieur, et al.
American Journal of Medical Genetics
|
December 26, 2001
Chromosome 10p11.2-p12.2 duplication: report of a patient and review of the literature
A Mégarbané, P Gosset, N Souraty, et al.
Mechanisms of Development
|
April 27, 2000
Regional and cellular specificity of the expression of TPRD, the tetratricopeptide Down syndrome gene, during human embryonic development
M Rachidi, C Lopes, S Gassanova, et al.
The Journal of Organic Chemistry
|
September 6, 1996
Hydrogen-Bonded Complexes of Diaminopyridines and Diaminotriazines: Opposite Effect of Acylation on Complex Stabilities
Felix H. Beijer, Rint P. Sijbesma, Jef A. J. M. Vekemans, et al.
American Journal of Human Genetics
|
April 17, 1999
Recurrent Williams-Beuren syndrome in a sibship suggestive of maternal germ-line mosaicism
A Kara-Mostefa, O Raoul, S Lyonnet, et al.
American Journal of Medical Genetics
|
March 13, 1995
Upper limb malformations in DiGeorge syndrome
V Cormier-Daire, L Iserin, D Théophile, et al.
Page
of 29