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J Feingold

Showing results (241-250 of 307) with videos related to

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Annals of Neurology|June 21, 2001
Evidence for digenic inheritance in a family with both febrile convulsions and temporal lobe epilepsy implicating chromosomes 18qter and 1q25-q31S Baulac, F Picard, A Herman, et al.
Archives of General Psychiatry|January 22, 1998
Association between the tryptophan hydroxylase gene and manic-depressive illnessF Bellivier, M Leboyer, P Courtet, et al.
Human Genetics|September 1, 1990
Frequency of the cystic fibrosis delta F508 mutation in a large sample of the French populationM Vidaud, C Ferec, O Attree, et al.
Neuroscience Letters|December 1, 1998
Serotonin transporter gene polymorphisms in patients with unipolar or bipolar depressionF Bellivier, C Henry, A Szöke, et al.
Journal of Medical Genetics|January 5, 2002
Trinucleotide repeat contraction: a pitfall in prenatal diagnosis of myotonic dystrophyJ Amiel, V Raclin, J M Jouannic, et al.
Annals of Human Genetics|January 1, 1973
Linkage studies of enzyme markers in man-mouse somatic cell hybridsC Billardon, Nguyen-Van-Cong, J Y Picard, et al.
Tissue Antigens|February 1, 1982
HLA and 21 hydroxylase deficiency (congenital and late onset adrenal hyperplasia) in the French populationP Couillin, R Rappaport, F Kuttenn, et al.
American Journal of Human Genetics|December 1, 1988
Clinical and molecular heterogeneity of phenylalanine hydroxylase deficiencies in FranceF Rey, M Berthelon, C Caillaud, et al.
American Journal of Medical Genetics|December 18, 1995
Lack of association between alcohol-dependence and D3 dopamine receptor gene in three independent samplesP Gorwood, M P Martres, J Adès, et al.
Human Genetics|January 26, 2002
Phenotypic variability at the TGF-beta1 locus in Camurati-Engelmann diseaseB Campos-Xavier, J M Saraiva, R Savarirayan, et al.
Pageof 31

Showing results (241-250 of 307) with videos related to

Sort By:
Pageof 31
Annals of Neurology|June 21, 2001
Evidence for digenic inheritance in a family with both febrile convulsions and temporal lobe epilepsy implicating chromosomes 18qter and 1q25-q31S Baulac, F Picard, A Herman, et al.
Archives of General Psychiatry|January 22, 1998
Association between the tryptophan hydroxylase gene and manic-depressive illnessF Bellivier, M Leboyer, P Courtet, et al.
Human Genetics|September 1, 1990
Frequency of the cystic fibrosis delta F508 mutation in a large sample of the French populationM Vidaud, C Ferec, O Attree, et al.
Neuroscience Letters|December 1, 1998
Serotonin transporter gene polymorphisms in patients with unipolar or bipolar depressionF Bellivier, C Henry, A Szöke, et al.
Journal of Medical Genetics|January 5, 2002
Trinucleotide repeat contraction: a pitfall in prenatal diagnosis of myotonic dystrophyJ Amiel, V Raclin, J M Jouannic, et al.
Annals of Human Genetics|January 1, 1973
Linkage studies of enzyme markers in man-mouse somatic cell hybridsC Billardon, Nguyen-Van-Cong, J Y Picard, et al.
Tissue Antigens|February 1, 1982
HLA and 21 hydroxylase deficiency (congenital and late onset adrenal hyperplasia) in the French populationP Couillin, R Rappaport, F Kuttenn, et al.
American Journal of Human Genetics|December 1, 1988
Clinical and molecular heterogeneity of phenylalanine hydroxylase deficiencies in FranceF Rey, M Berthelon, C Caillaud, et al.
American Journal of Medical Genetics|December 18, 1995
Lack of association between alcohol-dependence and D3 dopamine receptor gene in three independent samplesP Gorwood, M P Martres, J Adès, et al.
Human Genetics|January 26, 2002
Phenotypic variability at the TGF-beta1 locus in Camurati-Engelmann diseaseB Campos-Xavier, J M Saraiva, R Savarirayan, et al.
Pageof 31