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J Elion

Showing results (111-120 of 189) with videos related to

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Human Heredity|November 14, 1998
Heterogeneous ethnic distribution of the 844ins68 in the cystathionine beta-synthase geneR F Franco, J Elion, J Lavinha, et al.
Biochemical and Biophysical Research Communications|October 1, 1998
CFTR regions containing duodenum specific DNase I hypersensitive sites drive expression in intestinal crypt cells but not in fibroblastsI Dixméras, C Lapouméroulie, L P Tallec, et al.
British Journal of Haematology|December 3, 1999
The erythrocyte effects of haemoglobin O(ARAB)R L Nagel, R Krishnamoorthy, S Fattoum, et al.
Human Genetics|August 1, 1997
Polymorphism in exon 10 of the human coagulation factor V gene in a population at risk for sickle cell diseaseD Helley, C Besmond, R Ducrocq, et al.
Journal of Medical Screening|May 12, 1998
Compound heterozygosity Hb S/Hb Hope (beta 136 Gly-->Asp): a pitfall in the newborn screening for sickle cell diseaseR Ducrocq, A Bévier, A Leneveu, et al.
Science (New York, N.Y.)|November 5, 1997
Highly variable mutation rates in commensal and pathogenic Escherichia coliI Matic, M Radman, F Taddei, et al.
British Journal of Haematology|June 1, 1993
The spectrum of beta-thalassaemia in Algeria: possible origins of the molecular heterogeneity and a tentative diagnostic strategyC Bennani, R Tamouza, F Rouabhi, et al.
Diabetologia|March 1, 1990
HLA-DQB 1 codon 57 and genetic susceptibility to type 1 (insulin-dependent) diabetes mellitus in French childrenI Vallet-Colom, C Lévy-Marchal, D Zarrouk, et al.
European Journal of Human Genetics : EJHG|January 1, 1996
Distribution of CFTR mutations in cystic fibrosis patients of Tunisian origin: identification of two novel mutationsT Messaoud, C Verlingue, E Denamur, et al.
British Journal of Haematology|February 1, 1996
Deletion mapping indicates that MTS1 is the target of frequent deletions at chromosome 9p21 in paediatric acute lymphoblastic leukaemiasC Guidal-Giroux, B Gérard, H Cavé, et al.
Pageof 19

Showing results (111-120 of 189) with videos related to

Sort By:
Pageof 19
Human Heredity|November 14, 1998
Heterogeneous ethnic distribution of the 844ins68 in the cystathionine beta-synthase geneR F Franco, J Elion, J Lavinha, et al.
Biochemical and Biophysical Research Communications|October 1, 1998
CFTR regions containing duodenum specific DNase I hypersensitive sites drive expression in intestinal crypt cells but not in fibroblastsI Dixméras, C Lapouméroulie, L P Tallec, et al.
British Journal of Haematology|December 3, 1999
The erythrocyte effects of haemoglobin O(ARAB)R L Nagel, R Krishnamoorthy, S Fattoum, et al.
Human Genetics|August 1, 1997
Polymorphism in exon 10 of the human coagulation factor V gene in a population at risk for sickle cell diseaseD Helley, C Besmond, R Ducrocq, et al.
Journal of Medical Screening|May 12, 1998
Compound heterozygosity Hb S/Hb Hope (beta 136 Gly-->Asp): a pitfall in the newborn screening for sickle cell diseaseR Ducrocq, A Bévier, A Leneveu, et al.
Science (New York, N.Y.)|November 5, 1997
Highly variable mutation rates in commensal and pathogenic Escherichia coliI Matic, M Radman, F Taddei, et al.
British Journal of Haematology|June 1, 1993
The spectrum of beta-thalassaemia in Algeria: possible origins of the molecular heterogeneity and a tentative diagnostic strategyC Bennani, R Tamouza, F Rouabhi, et al.
Diabetologia|March 1, 1990
HLA-DQB 1 codon 57 and genetic susceptibility to type 1 (insulin-dependent) diabetes mellitus in French childrenI Vallet-Colom, C Lévy-Marchal, D Zarrouk, et al.
European Journal of Human Genetics : EJHG|January 1, 1996
Distribution of CFTR mutations in cystic fibrosis patients of Tunisian origin: identification of two novel mutationsT Messaoud, C Verlingue, E Denamur, et al.
British Journal of Haematology|February 1, 1996
Deletion mapping indicates that MTS1 is the target of frequent deletions at chromosome 9p21 in paediatric acute lymphoblastic leukaemiasC Guidal-Giroux, B Gérard, H Cavé, et al.
Pageof 19