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Prenatal Diagnosis
|
June 1, 1992
Peculiar haematological features of fetuses with triploidy
P Boulot, B Bachelard, G Lefort, et al.
Annales De Pathologie
|
December 29, 1998
[Application of the PRINS technique for chromosome examination in fetal cells present in maternal blood]
B Orsetti, G Lefort, P Boulot, et al.
Genetic Counseling (Geneva, Switzerland)
|
January 1, 1991
Epidemiology of diaphragmatic hernia in Languedoc-Roussillon
P Sarda, P Devaux, G Lefort, et al.
Clinical Genetics
|
January 1, 1992
Interstitial deletion of chromosome 1 del (1) (q32 q42): case report and review of the literature
P Sarda, G Lefort, S Taviaux, et al.
Cytogenetic and Genome Research
|
September 7, 2006
Multicolor PRINS and multicolor PNA
F Pellestor, P Paulasova, B Andréo, et al.
Annales De Genetique
|
January 1, 1992
Multiple congenital anomalies due to partial 2p13----2pter duplication resulting from an unbalanced X;2 translocation
P Sarda, G Lefort, P Devaux, et al.
Prenatal Diagnosis
|
November 25, 1998
Fetal cells in maternal blood: the use of primed in situ (PRINS) labelling technique for fetal cell detection and sex assessment
B Orsetti, G Lefort, P Boulot, et al.
Pathologie-Biologie
|
May 1, 1981
[Radioimmunological assay for antithyroglobulin antibodies, with the use of staphylococcal protein A as separating agents (author's transl)]
G Lefort, M J Lanet, D Ducassou, et al.
Chirurgie Pediatrique
|
January 1, 1980
[Right congenital diaphragmatic hernia with systemic artery (author's transl)]
H Mourad, G Lefort, Y Jacob, et al.
Journal of Nuclear Medicine : Official Publication, Society of Nuclear Medicine
|
September 1, 1988
Thallium-201 imaging in the follow-up of differentiated thyroid carcinoma
A J Brendel, M Guyot, R Jeandot, et al.
Page
of 12
Search research articles
Search
Showing results (31-40 of 114) with videos related to
Sort By:
Page
of 12
Prenatal Diagnosis
|
June 1, 1992
Peculiar haematological features of fetuses with triploidy
P Boulot, B Bachelard, G Lefort, et al.
Annales De Pathologie
|
December 29, 1998
[Application of the PRINS technique for chromosome examination in fetal cells present in maternal blood]
B Orsetti, G Lefort, P Boulot, et al.
Genetic Counseling (Geneva, Switzerland)
|
January 1, 1991
Epidemiology of diaphragmatic hernia in Languedoc-Roussillon
P Sarda, P Devaux, G Lefort, et al.
Clinical Genetics
|
January 1, 1992
Interstitial deletion of chromosome 1 del (1) (q32 q42): case report and review of the literature
P Sarda, G Lefort, S Taviaux, et al.
Cytogenetic and Genome Research
|
September 7, 2006
Multicolor PRINS and multicolor PNA
F Pellestor, P Paulasova, B Andréo, et al.
Annales De Genetique
|
January 1, 1992
Multiple congenital anomalies due to partial 2p13----2pter duplication resulting from an unbalanced X;2 translocation
P Sarda, G Lefort, P Devaux, et al.
Prenatal Diagnosis
|
November 25, 1998
Fetal cells in maternal blood: the use of primed in situ (PRINS) labelling technique for fetal cell detection and sex assessment
B Orsetti, G Lefort, P Boulot, et al.
Pathologie-Biologie
|
May 1, 1981
[Radioimmunological assay for antithyroglobulin antibodies, with the use of staphylococcal protein A as separating agents (author's transl)]
G Lefort, M J Lanet, D Ducassou, et al.
Chirurgie Pediatrique
|
January 1, 1980
[Right congenital diaphragmatic hernia with systemic artery (author's transl)]
H Mourad, G Lefort, Y Jacob, et al.
Journal of Nuclear Medicine : Official Publication, Society of Nuclear Medicine
|
September 1, 1988
Thallium-201 imaging in the follow-up of differentiated thyroid carcinoma
A J Brendel, M Guyot, R Jeandot, et al.
Page
of 12