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J Godet

Showing results (61-70 of 71) with videos related to

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American Journal of Hematology|April 1, 1988
Asymptomatic association of hemoglobin Dunn (alpha 6[A4]Asp----Asn) and hemoglobin O-Arab (beta 121[GH4]Glu----Lys) in a Moroccan manF Baklouti, A Francina, E Dorléac, et al.
Human Genetics|October 1, 1990
Evidence that expression of Sp alpha I/65 hereditary elliptocytosis is compounded by a genetic factor that is linked to the homologous alpha-spectrin alleleD Guetarni, A F Roux, N Alloisio, et al.
Journal of Medical Genetics|May 12, 2000
A novel C202F mutation in the connexin26 gene (GJB2) associated with autosomal dominant isolated hearing lossL Morlé, M Bozon, N Alloisio, et al.
European Journal of Human Genetics : EJHG|April 10, 1999
Mutation in the zonadhesin-like domain of alpha-tectorin associated with autosomal dominant non-syndromic hearing lossN Alloisio, L Morlé, M Bozon, et al.
Blood|August 1, 1989
Spectrin Tunis (Sp alpha I/78), an elliptocytogenic variant, is due to the CGG----TGG codon change (Arg----Trp) at position 35 of the alpha I domainL Morlé, F Morlé, A F Roux, et al.
American Journal of Human Genetics|October 18, 2000
A locus for autosomal dominant colobomatous microphthalmia maps to chromosome 15q12-q15L Morlé, M Bozon, J C Zech, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|May 20, 1999
Wagner vitreoretinal degeneration with genetic linkage refinement on chromosome 5q13-q14J C Zech, L Morlé, P Vincent, et al.
Clinical Genetics|April 27, 2011
Hippocampal dysgenesis and variable neuropsychiatric phenotypes in patients with Bardet-Biedl syndrome underline complex CNS impact of primary ciliaV Bennouna-Greene, S Kremer, C Stoetzel, et al.
Journal of Investigational Allergology & Clinical Immunology|November 15, 2022
Sputum Inflammatory Patterns Are Associated With Distinct Clinical Characteristics in Patients with Occupational Asthma Independently of the Causal AgentN Migueres, O Vandenplas, J Walusiak-Skorupa, et al.
ESMO Open|April 30, 2021
Discordance between immunochemistry of mismatch repair proteins and molecular testing of microsatellite instability in colorectal cancerA Guyot D'Asnières De Salins, G Tachon, R Cohen, et al.
Pageof 8

Showing results (61-70 of 71) with videos related to

Sort By:
Pageof 8
American Journal of Hematology|April 1, 1988
Asymptomatic association of hemoglobin Dunn (alpha 6[A4]Asp----Asn) and hemoglobin O-Arab (beta 121[GH4]Glu----Lys) in a Moroccan manF Baklouti, A Francina, E Dorléac, et al.
Human Genetics|October 1, 1990
Evidence that expression of Sp alpha I/65 hereditary elliptocytosis is compounded by a genetic factor that is linked to the homologous alpha-spectrin alleleD Guetarni, A F Roux, N Alloisio, et al.
Journal of Medical Genetics|May 12, 2000
A novel C202F mutation in the connexin26 gene (GJB2) associated with autosomal dominant isolated hearing lossL Morlé, M Bozon, N Alloisio, et al.
European Journal of Human Genetics : EJHG|April 10, 1999
Mutation in the zonadhesin-like domain of alpha-tectorin associated with autosomal dominant non-syndromic hearing lossN Alloisio, L Morlé, M Bozon, et al.
Blood|August 1, 1989
Spectrin Tunis (Sp alpha I/78), an elliptocytogenic variant, is due to the CGG----TGG codon change (Arg----Trp) at position 35 of the alpha I domainL Morlé, F Morlé, A F Roux, et al.
American Journal of Human Genetics|October 18, 2000
A locus for autosomal dominant colobomatous microphthalmia maps to chromosome 15q12-q15L Morlé, M Bozon, J C Zech, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|May 20, 1999
Wagner vitreoretinal degeneration with genetic linkage refinement on chromosome 5q13-q14J C Zech, L Morlé, P Vincent, et al.
Clinical Genetics|April 27, 2011
Hippocampal dysgenesis and variable neuropsychiatric phenotypes in patients with Bardet-Biedl syndrome underline complex CNS impact of primary ciliaV Bennouna-Greene, S Kremer, C Stoetzel, et al.
Journal of Investigational Allergology & Clinical Immunology|November 15, 2022
Sputum Inflammatory Patterns Are Associated With Distinct Clinical Characteristics in Patients with Occupational Asthma Independently of the Causal AgentN Migueres, O Vandenplas, J Walusiak-Skorupa, et al.
ESMO Open|April 30, 2021
Discordance between immunochemistry of mismatch repair proteins and molecular testing of microsatellite instability in colorectal cancerA Guyot D'Asnières De Salins, G Tachon, R Cohen, et al.
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