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Journal of Medical Genetics
|
March 10, 2001
A new case of exomphalos, short limbs, and macrogonadism syndrome
G Viot, E Pannier, L Faivre, et al.
American Journal of Medical Genetics. Part A
|
August 2, 2005
Microcephaly is not mandatory for the diagnosis of mosaic variegated aneuploidy syndrome
P Callier, L Faivre, V Cusin, et al.
Prenatal Diagnosis
|
November 25, 1998
Prenatal diagnosis of an 8p23.1 deletion in a fetus with a diaphragmatic hernia and review of the literature
L Faivre, N Morichon-Delvallez, G Viot, et al.
American Journal of Medical Genetics. Part A
|
December 12, 2002
Mild phenotype in a 15-year-old boy with Pallister-Killian syndrome
D Genevieve, V Cormier-Daire, D Sanlaville, et al.
Helvetica Chimica Acta
|
January 1, 1970
[C-glycosides. 3. 1,3-dipolar cycloaddition on nitrile and nitrilimine oxides]
J M Tronchet, A Jottearand, N Le Hong, et al.
Transplantation Proceedings
|
June 19, 2001
FK 506 dose in transplantation: from theory to practice
L Faivre, S Saoudi, A Astier, et al.
Current Research in Translational Medicine
|
October 22, 2016
<sup>18</sup>F-FDG labelling of hematopoietic stem cells: Dynamic study of bone marrow homing by PET-CT imaging and impact on cell functionality
L Faivre, M Chaussard, L Vercellino, et al.
Journal of Medical Genetics
|
June 19, 2002
Towards a suggestive facial dysmorphism in adenylosuccinate lyase deficiency?
M Holder-Espinasse, S Marie, G Bourrouillou, et al.
Prenatal Diagnosis
|
March 12, 1999
Prenatal detection of a 1p36 deletion in a fetus with multiple malformations and a review of the literature
L Faivre, N Morichon-Delvallez, G Viot, et al.
American Journal of Medical Genetics
|
March 10, 2001
Mazabraud syndrome in two patients: clinical overlap with McCune-Albright syndrome
L Faivre, A Nivelon-Chevallier, M L Kottler, et al.
Page
of 14
Search research articles
Search
Showing results (31-40 of 131) with videos related to
Sort By:
Page
of 14
Journal of Medical Genetics
|
March 10, 2001
A new case of exomphalos, short limbs, and macrogonadism syndrome
G Viot, E Pannier, L Faivre, et al.
American Journal of Medical Genetics. Part A
|
August 2, 2005
Microcephaly is not mandatory for the diagnosis of mosaic variegated aneuploidy syndrome
P Callier, L Faivre, V Cusin, et al.
Prenatal Diagnosis
|
November 25, 1998
Prenatal diagnosis of an 8p23.1 deletion in a fetus with a diaphragmatic hernia and review of the literature
L Faivre, N Morichon-Delvallez, G Viot, et al.
American Journal of Medical Genetics. Part A
|
December 12, 2002
Mild phenotype in a 15-year-old boy with Pallister-Killian syndrome
D Genevieve, V Cormier-Daire, D Sanlaville, et al.
Helvetica Chimica Acta
|
January 1, 1970
[C-glycosides. 3. 1,3-dipolar cycloaddition on nitrile and nitrilimine oxides]
J M Tronchet, A Jottearand, N Le Hong, et al.
Transplantation Proceedings
|
June 19, 2001
FK 506 dose in transplantation: from theory to practice
L Faivre, S Saoudi, A Astier, et al.
Current Research in Translational Medicine
|
October 22, 2016
<sup>18</sup>F-FDG labelling of hematopoietic stem cells: Dynamic study of bone marrow homing by PET-CT imaging and impact on cell functionality
L Faivre, M Chaussard, L Vercellino, et al.
Journal of Medical Genetics
|
June 19, 2002
Towards a suggestive facial dysmorphism in adenylosuccinate lyase deficiency?
M Holder-Espinasse, S Marie, G Bourrouillou, et al.
Prenatal Diagnosis
|
March 12, 1999
Prenatal detection of a 1p36 deletion in a fetus with multiple malformations and a review of the literature
L Faivre, N Morichon-Delvallez, G Viot, et al.
American Journal of Medical Genetics
|
March 10, 2001
Mazabraud syndrome in two patients: clinical overlap with McCune-Albright syndrome
L Faivre, A Nivelon-Chevallier, M L Kottler, et al.
Page
of 14