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Journal De Genetique Humaine
|
June 1, 1985
[Effect of metoclopramide in a subject at risk for Huntington's chorea]
A Nivelon-Chevallier, M Giroud, J L Fabre, et al.
Neuro-Chirurgie
|
January 1, 1982
[Intracranial aneurysm and polycystic kidneys]
A Thierry, J L Sautreaux, G Rifle, et al.
Journal De Genetique Humaine
|
May 1, 1987
[Second prenatal diagnosis in a familial form of male pseudohermaphroditism caused by 17 keto-reductase deficiency: prediction confirmed by a normal third male infant]
J L Nivelon, M G Forest, A Nivelon-Chevallier, et al.
Journal De Gynecologie, Obstetrique Et Biologie De La Reproduction
|
January 1, 1980
[Congenital malformations. 1,238 cases of malformed infants in a 25-year (1950 to 1974) continuous series of 49,665 deliveries. Epidemiological and statistical study]
P Bugnon, A Nivelon-Chevallier, A Mavel, et al.
Journal De Genetique Humaine
|
November 1, 1982
[Polydactyly]
B Le Marec, H Bracq, C Lambotte, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM
|
January 25, 2002
Association of Marfan's syndrome and Turner's syndrome
C Thauvin-Robinet, J V De Monléon, A Nivelon-Chevallier, et al.
Journal De Genetique Humaine
|
January 1, 1988
[Translocation (X; Y) and genetic counseling]
F Mugneret, I Sidaner, A Nivelon-Chevallier, et al.
Neurology
|
May 9, 2001
A major locus for several phenotypes of myoclonus--dystonia on chromosome 7q
M Vidailhet, J Tassin, F Durif, et al.
Annales De Dermatologie Et De Venereologie
|
January 1, 1995
[Congenital pachyonychia, neurofibromatosis and sensory-motor polyneuropathy]
A F Bensa, S Dalac, F Beer, et al.
Journal De Genetique Humaine
|
May 1, 1987
[An XX male newborn infant. A genetic and endocrinologic study]
J L Nivelon, E Seboun, M Fellous, et al.
Page
of 5
Search research articles
Search
Showing results (11-20 of 48) with videos related to
Sort By:
Page
of 5
Journal De Genetique Humaine
|
June 1, 1985
[Effect of metoclopramide in a subject at risk for Huntington's chorea]
A Nivelon-Chevallier, M Giroud, J L Fabre, et al.
Neuro-Chirurgie
|
January 1, 1982
[Intracranial aneurysm and polycystic kidneys]
A Thierry, J L Sautreaux, G Rifle, et al.
Journal De Genetique Humaine
|
May 1, 1987
[Second prenatal diagnosis in a familial form of male pseudohermaphroditism caused by 17 keto-reductase deficiency: prediction confirmed by a normal third male infant]
J L Nivelon, M G Forest, A Nivelon-Chevallier, et al.
Journal De Gynecologie, Obstetrique Et Biologie De La Reproduction
|
January 1, 1980
[Congenital malformations. 1,238 cases of malformed infants in a 25-year (1950 to 1974) continuous series of 49,665 deliveries. Epidemiological and statistical study]
P Bugnon, A Nivelon-Chevallier, A Mavel, et al.
Journal De Genetique Humaine
|
November 1, 1982
[Polydactyly]
B Le Marec, H Bracq, C Lambotte, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM
|
January 25, 2002
Association of Marfan's syndrome and Turner's syndrome
C Thauvin-Robinet, J V De Monléon, A Nivelon-Chevallier, et al.
Journal De Genetique Humaine
|
January 1, 1988
[Translocation (X; Y) and genetic counseling]
F Mugneret, I Sidaner, A Nivelon-Chevallier, et al.
Neurology
|
May 9, 2001
A major locus for several phenotypes of myoclonus--dystonia on chromosome 7q
M Vidailhet, J Tassin, F Durif, et al.
Annales De Dermatologie Et De Venereologie
|
January 1, 1995
[Congenital pachyonychia, neurofibromatosis and sensory-motor polyneuropathy]
A F Bensa, S Dalac, F Beer, et al.
Journal De Genetique Humaine
|
May 1, 1987
[An XX male newborn infant. A genetic and endocrinologic study]
J L Nivelon, E Seboun, M Fellous, et al.
Page
of 5