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A Delahaye

Showing results (11-20 of 18) with videos related to

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Journal of Medical Genetics|September 25, 2008
2q23.1 microdeletion identified by array comparative genomic hybridisation: an emerging phenotype with Angelman-like features?S Jaillard, C Dubourg, M Gérard-Blanluet, et al.
Blood|July 27, 2001
Myelopoiesis in the zebrafish, Danio rerioC M Bennett, J P Kanki, J Rhodes, et al.
Clinical Genetics|May 18, 2018
NR4A2 haploinsufficiency is associated with intellectual disability and autism spectrum disorderJ Lévy, S Grotto, C Mignot, et al.
Clinical Genetics|July 31, 2007
Familial CHARGE syndrome because of CHD7 mutation: clinical intra- and interfamilial variabilityA Delahaye, Y Sznajer, S Lyonnet, et al.
International Journal of Cardiology|December 3, 2014
One-year outcome following biological or mechanical valve replacement for infective endocarditisF Delahaye, V H Chu, J Altclas, et al.
Clinical Genetics|July 5, 2011
What can we learn from old microdeletion syndromes using array-CGH screening?A L Mosca-Boidron, S Bouquillon, L Faivre, et al.
Clinical Genetics|December 25, 2015
A series of 38 novel germline and somatic mutations of NIPBL in Cornelia de Lange syndromeM Nizon, M Henry, C Michot, et al.
Clinical Genetics|September 17, 2013
Molecular findings and clinical data in a cohort of 150 patients with anophthalmia/microphthalmiaN Chassaing, A Causse, A Vigouroux, et al.
Pageof 2

Showing results (11-20 of 18) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 18 results.
Journal of Medical Genetics|September 25, 2008
2q23.1 microdeletion identified by array comparative genomic hybridisation: an emerging phenotype with Angelman-like features?S Jaillard, C Dubourg, M Gérard-Blanluet, et al.
Blood|July 27, 2001
Myelopoiesis in the zebrafish, Danio rerioC M Bennett, J P Kanki, J Rhodes, et al.
Clinical Genetics|May 18, 2018
NR4A2 haploinsufficiency is associated with intellectual disability and autism spectrum disorderJ Lévy, S Grotto, C Mignot, et al.
Clinical Genetics|July 31, 2007
Familial CHARGE syndrome because of CHD7 mutation: clinical intra- and interfamilial variabilityA Delahaye, Y Sznajer, S Lyonnet, et al.
International Journal of Cardiology|December 3, 2014
One-year outcome following biological or mechanical valve replacement for infective endocarditisF Delahaye, V H Chu, J Altclas, et al.
Clinical Genetics|July 5, 2011
What can we learn from old microdeletion syndromes using array-CGH screening?A L Mosca-Boidron, S Bouquillon, L Faivre, et al.
Clinical Genetics|December 25, 2015
A series of 38 novel germline and somatic mutations of NIPBL in Cornelia de Lange syndromeM Nizon, M Henry, C Michot, et al.
Clinical Genetics|September 17, 2013
Molecular findings and clinical data in a cohort of 150 patients with anophthalmia/microphthalmiaN Chassaing, A Causse, A Vigouroux, et al.
Pageof 2