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J Feingold

Showing results (221-230 of 307) with videos related to

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Tropical Medicine & International Health : TM & IH|September 28, 1999
Genetic epidemiology of host predisposition microfilaraemia in human loiasisA Garcia, L Abel, M Cot, et al.
Genetic Counseling (Geneva, Switzerland)|January 1, 1996
Implications of prenatal diagnosis of sickle cell diseaseM de Montalembert, M Guilloud-Bataille, A Ducros, et al.
Journal of the Neurological Sciences|March 1, 1995
Diagnosis of "sporadic" Huntington's diseaseA Dürr, C Dodé, V Hahn, et al.
Journal De Genetique Humaine|November 1, 1976
[The genetics of congenital glaucoma: a study of 231 cases]M L Briard, J Feingold, J Kaplan, et al.
Biological Psychiatry|March 15, 1991
Cytogenetic studies of familial schizophrenicsP Gorwood, M Leboyer, D Hillaire, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|March 7, 1998
Are cognitive changes the first symptoms of Huntington's disease? A study of gene carriersV Hahn-Barma, B Deweer, A Dürr, et al.
Annals of Human Biology|July 1, 1991
Population genetics of abnormal haemoglobins in Burkina Faso, west AfricaR Devoucoux, C Hurpin, D Baudon, et al.
Gastroenterologie Clinique Et Biologique|February 1, 1979
[Diabetogenous factors in chronic pancreatitis (author's transl)]N N Lyra de Lacerda, J Feingold, P Bernades, et al.
American Journal of Ophthalmology|March 25, 1998
The epsilon4 allele of the apolipoprotein E gene as a potential protective factor for exudative age-related macular degenerationE H Souied, P Benlian, P Amouyel, et al.
Clinical Genetics|December 8, 1998
Detection of more than 91% cystic fibrosis mutations in a sample of the population from Reunion Island and identification of two novel mutations (A309G, S1255L) and one novel polymorphism (L49L)F Cartault, J Steffann, D Vidaud, et al.
Pageof 31

Showing results (221-230 of 307) with videos related to

Sort By:
Pageof 31
Tropical Medicine & International Health : TM & IH|September 28, 1999
Genetic epidemiology of host predisposition microfilaraemia in human loiasisA Garcia, L Abel, M Cot, et al.
Genetic Counseling (Geneva, Switzerland)|January 1, 1996
Implications of prenatal diagnosis of sickle cell diseaseM de Montalembert, M Guilloud-Bataille, A Ducros, et al.
Journal of the Neurological Sciences|March 1, 1995
Diagnosis of "sporadic" Huntington's diseaseA Dürr, C Dodé, V Hahn, et al.
Journal De Genetique Humaine|November 1, 1976
[The genetics of congenital glaucoma: a study of 231 cases]M L Briard, J Feingold, J Kaplan, et al.
Biological Psychiatry|March 15, 1991
Cytogenetic studies of familial schizophrenicsP Gorwood, M Leboyer, D Hillaire, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|March 7, 1998
Are cognitive changes the first symptoms of Huntington's disease? A study of gene carriersV Hahn-Barma, B Deweer, A Dürr, et al.
Annals of Human Biology|July 1, 1991
Population genetics of abnormal haemoglobins in Burkina Faso, west AfricaR Devoucoux, C Hurpin, D Baudon, et al.
Gastroenterologie Clinique Et Biologique|February 1, 1979
[Diabetogenous factors in chronic pancreatitis (author's transl)]N N Lyra de Lacerda, J Feingold, P Bernades, et al.
American Journal of Ophthalmology|March 25, 1998
The epsilon4 allele of the apolipoprotein E gene as a potential protective factor for exudative age-related macular degenerationE H Souied, P Benlian, P Amouyel, et al.
Clinical Genetics|December 8, 1998
Detection of more than 91% cystic fibrosis mutations in a sample of the population from Reunion Island and identification of two novel mutations (A309G, S1255L) and one novel polymorphism (L49L)F Cartault, J Steffann, D Vidaud, et al.
Pageof 31