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Journal De Genetique Humaine
|
September 1, 1981
[Practical and psychological difficulties of a consanguinity study. Apropos of a family with a 2q +, 6q-translocation]
R Mettey, A Hoppeler, T Fizazi, et al.
Annales De Pediatrie
|
June 1, 1985
[Severe rheumatoid purpura. Histology of digestive manifestations and therapeutic trial using plasma exchange]
G Masson, R Mettey, P Doeuvre, et al.
Clinical Biochemistry
|
December 1, 1992
Congenital hypomagnesemia: alternatives to tissue biopsies for monitoring body magnesium status
O Guillard, R Mettey, J C Lecron, et al.
Archives Francaises De Pediatrie
|
April 1, 1990
[Neonatal primary hyperparathyroidism, parathyroid adenoma, chromosomal deletion: an approach to localizing the gene?]
R Mettey, M P Peyre, J Battin, et al.
Journal De Genetique Humaine
|
August 1, 1987
[Hydrocephalus and the Goldenhar syndrome]
R Mettey, G Masson, M P Peyre, et al.
Magnesium Research
|
December 1, 1990
Severe selective magnesium malabsorption: tests of tolerance of oral magnesium supplements
R Mettey, O Guillard, P Merle, et al.
Pediatrie
|
January 1, 1989
[Congenital pseudohypoaldosteronism: apropos of 6 cases]
C Cessans, M Berthier, D Bonneau, et al.
Annales De Radiologie
|
December 1, 1984
[Spontaneously regressive anuria in a newborn infant. Value of echography]
R Mettey, D Barret, G Duclos, et al.
Journal of Internal Medicine
|
June 21, 2002
Unexpected toxicity induced by magnesium orotate treatment in congenital hypomagnesemia
O Guillard, A Piriou, B Fauconneau, et al.
Clinical Genetics
|
March 1, 1992
Monosomy 6q: report on four new cases
C Valtat, D Galliano, R Mettey, et al.
Page
of 4
Search research articles
Search
Showing results (11-20 of 33) with videos related to
Sort By:
Page
of 4
Journal De Genetique Humaine
|
September 1, 1981
[Practical and psychological difficulties of a consanguinity study. Apropos of a family with a 2q +, 6q-translocation]
R Mettey, A Hoppeler, T Fizazi, et al.
Annales De Pediatrie
|
June 1, 1985
[Severe rheumatoid purpura. Histology of digestive manifestations and therapeutic trial using plasma exchange]
G Masson, R Mettey, P Doeuvre, et al.
Clinical Biochemistry
|
December 1, 1992
Congenital hypomagnesemia: alternatives to tissue biopsies for monitoring body magnesium status
O Guillard, R Mettey, J C Lecron, et al.
Archives Francaises De Pediatrie
|
April 1, 1990
[Neonatal primary hyperparathyroidism, parathyroid adenoma, chromosomal deletion: an approach to localizing the gene?]
R Mettey, M P Peyre, J Battin, et al.
Journal De Genetique Humaine
|
August 1, 1987
[Hydrocephalus and the Goldenhar syndrome]
R Mettey, G Masson, M P Peyre, et al.
Magnesium Research
|
December 1, 1990
Severe selective magnesium malabsorption: tests of tolerance of oral magnesium supplements
R Mettey, O Guillard, P Merle, et al.
Pediatrie
|
January 1, 1989
[Congenital pseudohypoaldosteronism: apropos of 6 cases]
C Cessans, M Berthier, D Bonneau, et al.
Annales De Radiologie
|
December 1, 1984
[Spontaneously regressive anuria in a newborn infant. Value of echography]
R Mettey, D Barret, G Duclos, et al.
Journal of Internal Medicine
|
June 21, 2002
Unexpected toxicity induced by magnesium orotate treatment in congenital hypomagnesemia
O Guillard, A Piriou, B Fauconneau, et al.
Clinical Genetics
|
March 1, 1992
Monosomy 6q: report on four new cases
C Valtat, D Galliano, R Mettey, et al.
Page
of 4