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Cédric Le Caignec

Showing results (1-10 of 99) with videos related to

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Medecine Sciences : M/S|July 2, 2011
[Human diseases and NOTCH receptors]Cédric Le Caignec
Revue Medicale Suisse|July 2, 2026
Cédric Le Caignec, Marc Abramowicz
Genome Biology|February 17, 2009
Copy number variation goes clinicalCédric Le Caignec, Richard Redon
Revue Medicale Suisse|July 2, 2026
[Genetic medicine illustrated by three key syndromes]Ailsa Craig, Cédric Le Caignec, Christel Tran
Prenatal Diagnosis|July 26, 2006
Two independent rare events--a mutation in the RUNX2 gene and a de novo balanced translocation--in a fetus with cleidocranial dysplasia: pitfall in prenatal diagnosisCédric Le Caignec, Norbert Winer, Henri-Jean Philippe, et al.
American Journal of Medical Genetics. Part A|May 7, 2011
Multiple capillary skin malformations, epilepsy, microcephaly, mental retardation, hypoplasia of the distal phalanges: report of a new case and further delineation of a new syndromeBertrand Isidor, Sébastien Barbarot, Claire Bénéteau, et al.
American Journal of Medical Genetics. Part A|December 17, 2009
Deletion of the CUL4B gene in a boy with mental retardation, minor facial anomalies, short stature, hypogonadism, and ataxiaBertrand Isidor, Olivier Pichon, Sabine Baron, et al.
European Journal of Medical Genetics|June 1, 2018
Oro-dental phenotype in patients with RUNX2 duplicationLaure Merametdjian, Tony Prud'Homme, Cédric Le Caignec, et al.
European Journal of Medical Genetics|November 26, 2018
A de novo 2q37.2 deletion encompassing AGAP1 and SH3BP4 in a patient with autism and intellectual disabilityMathilde Pacault, Mathilde Nizon, Olivier Pichon, et al.
European Journal of Medical Genetics|September 24, 2005
Interstitial 6q deletion: clinical and array CGH characterisation of a new patientCédric Le Caignec, Ann Swillen, Elvire Van Asche, et al.
Pageof 10

Showing results (1-10 of 99) with videos related to

Sort By:
Pageof 10
Medecine Sciences : M/S|July 2, 2011
[Human diseases and NOTCH receptors]Cédric Le Caignec
Revue Medicale Suisse|July 2, 2026
Cédric Le Caignec, Marc Abramowicz
Genome Biology|February 17, 2009
Copy number variation goes clinicalCédric Le Caignec, Richard Redon
Revue Medicale Suisse|July 2, 2026
[Genetic medicine illustrated by three key syndromes]Ailsa Craig, Cédric Le Caignec, Christel Tran
Prenatal Diagnosis|July 26, 2006
Two independent rare events--a mutation in the RUNX2 gene and a de novo balanced translocation--in a fetus with cleidocranial dysplasia: pitfall in prenatal diagnosisCédric Le Caignec, Norbert Winer, Henri-Jean Philippe, et al.
American Journal of Medical Genetics. Part A|May 7, 2011
Multiple capillary skin malformations, epilepsy, microcephaly, mental retardation, hypoplasia of the distal phalanges: report of a new case and further delineation of a new syndromeBertrand Isidor, Sébastien Barbarot, Claire Bénéteau, et al.
American Journal of Medical Genetics. Part A|December 17, 2009
Deletion of the CUL4B gene in a boy with mental retardation, minor facial anomalies, short stature, hypogonadism, and ataxiaBertrand Isidor, Olivier Pichon, Sabine Baron, et al.
European Journal of Medical Genetics|June 1, 2018
Oro-dental phenotype in patients with RUNX2 duplicationLaure Merametdjian, Tony Prud'Homme, Cédric Le Caignec, et al.
European Journal of Medical Genetics|November 26, 2018
A de novo 2q37.2 deletion encompassing AGAP1 and SH3BP4 in a patient with autism and intellectual disabilityMathilde Pacault, Mathilde Nizon, Olivier Pichon, et al.
European Journal of Medical Genetics|September 24, 2005
Interstitial 6q deletion: clinical and array CGH characterisation of a new patientCédric Le Caignec, Ann Swillen, Elvire Van Asche, et al.
Pageof 10