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J Lafourcade

Showing results (11-20 of 25) with videos related to

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Annales De Genetique|September 1, 1976
[45, X/47, XY, +13 mosaicism in a 19-year-old girl]M Prieur, B Dutrillaux, J Lafourcade, et al.
Annales De Genetique|January 1, 1982
[X chromosome fragility and effects of trimethoprim]J Lejeune, N Legrand, J Lafourcade, et al.
Annales De Genetique|June 1, 1976
[The r(22) syndrome, Apropos of 4 new cases]M O Rethore, B Noël, J Couturier, et al.
Annales De Genetique|March 1, 1972
[Familial segregation of a t(5p-;13q+). Complementary analysis from specimens preserved in liquid nitrogen]S Carpentier, B Dutrillaux, J Lafourcade, et al.
La Semaine Des Hopitaux : Organe Fonde Par L'Association D'Enseignement Medical Des Hopitaux De Paris|July 7, 1983
[17p trisomy]M O Rethoré, F Renault, J Lafourcade, et al.
Annales De Genetique|March 1, 1970
[Free 21 trisomy in mother and daughter]M O Rethoré, J Lafourcade, M Prieur, et al.
Neuro-Chirurgie|January 1, 1989
[Successful separation in 1974 of craniopagus twins united at the vertex. Indications, technics, follow-up after 14 years]B Pertuiset, J Lafourcade, P Viars, et al.
The Journal of Pediatrics|February 1, 1981
Homocystinuria caused by 5,10-methylenetetrahydrofolate reductase deficiency: a case in an infant responding to methionine, folinic acid, pyridoxine, and vitamin B12 therapyJ P Harpey, D S Rosenblatt, B A Cooper, et al.
Annales De Pediatrie|December 1, 1977
[Primary fibroelastosis of the endocardium. Genetic advice]C Roy, S Duriez, M Prieur, et al.
Archives Francaises De Pediatrie|February 1, 1970
[Systemic lupus erythematosus. Transmission of clinical manifestations and biological factors from the mother to the newborn]J Cruveiller, J P Harpey, P Veron, et al.
Pageof 3

Showing results (11-20 of 25) with videos related to

Sort By:
Pageof 3
Annales De Genetique|September 1, 1976
[45, X/47, XY, +13 mosaicism in a 19-year-old girl]M Prieur, B Dutrillaux, J Lafourcade, et al.
Annales De Genetique|January 1, 1982
[X chromosome fragility and effects of trimethoprim]J Lejeune, N Legrand, J Lafourcade, et al.
Annales De Genetique|June 1, 1976
[The r(22) syndrome, Apropos of 4 new cases]M O Rethore, B Noël, J Couturier, et al.
Annales De Genetique|March 1, 1972
[Familial segregation of a t(5p-;13q+). Complementary analysis from specimens preserved in liquid nitrogen]S Carpentier, B Dutrillaux, J Lafourcade, et al.
La Semaine Des Hopitaux : Organe Fonde Par L'Association D'Enseignement Medical Des Hopitaux De Paris|July 7, 1983
[17p trisomy]M O Rethoré, F Renault, J Lafourcade, et al.
Annales De Genetique|March 1, 1970
[Free 21 trisomy in mother and daughter]M O Rethoré, J Lafourcade, M Prieur, et al.
Neuro-Chirurgie|January 1, 1989
[Successful separation in 1974 of craniopagus twins united at the vertex. Indications, technics, follow-up after 14 years]B Pertuiset, J Lafourcade, P Viars, et al.
The Journal of Pediatrics|February 1, 1981
Homocystinuria caused by 5,10-methylenetetrahydrofolate reductase deficiency: a case in an infant responding to methionine, folinic acid, pyridoxine, and vitamin B12 therapyJ P Harpey, D S Rosenblatt, B A Cooper, et al.
Annales De Pediatrie|December 1, 1977
[Primary fibroelastosis of the endocardium. Genetic advice]C Roy, S Duriez, M Prieur, et al.
Archives Francaises De Pediatrie|February 1, 1970
[Systemic lupus erythematosus. Transmission of clinical manifestations and biological factors from the mother to the newborn]J Cruveiller, J P Harpey, P Veron, et al.
Pageof 3