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A C Tabet

Showing results (1-10 of 12) with videos related to

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Annales De Genetique|November 6, 2001
Heteromorphism 18ph+ : with or without reproductive consequences?A C Tabet, J M Dupont, A Lebbar, et al.
Prenatal Diagnosis|September 24, 2004
Prenatal diagnosis and characterization of an analphoid marker chromosome 16A C Tabet, P Gosset, H Elghezal, et al.
European Journal of Medical Genetics|May 21, 2009
Chromosome 22q13.3 deletion syndrome with a de novo interstitial 22q13.3 cryptic deletion disrupting SHANK3A Delahaye, A Toutain, A Aboura, et al.
Prenatal Diagnosis|September 6, 2001
Cytogenetic analysis of trophoblasts by comparative genomic hybridization in embryo-fetal development anomaliesA C Tabet, A Aboura, M C Dauge, et al.
Clinical Genetics|March 7, 2018
EFNB2 haploinsufficiency causes a syndromic neurodevelopmental disorderJ Lévy, D Haye, N Marziliano, et al.
Clinical Genetics|May 11, 2011
3D position of pericentromeric heterochromatin within the nucleus of a patient with ICF syndromeC Dupont, F Guimiot, L Perrin, et al.
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.
Clinical Genetics|February 17, 2018
INTU-related oral-facial-digital syndrome type VI: A confirmatory reportA-L Bruel, J Levy, N Elenga, 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.
Prenatal Diagnosis|February 3, 2007
Semilobar holoprosencephaly prenatal diagnosis: an unexpected complex rearrangement in a de novo apparently balanced reciprocal translocation on karyotypeS Kanafani, A Aboura, E Pipiras, et al.
Pageof 2

Showing results (1-10 of 12) with videos related to

Sort By:
Pageof 2
Annales De Genetique|November 6, 2001
Heteromorphism 18ph+ : with or without reproductive consequences?A C Tabet, J M Dupont, A Lebbar, et al.
Prenatal Diagnosis|September 24, 2004
Prenatal diagnosis and characterization of an analphoid marker chromosome 16A C Tabet, P Gosset, H Elghezal, et al.
European Journal of Medical Genetics|May 21, 2009
Chromosome 22q13.3 deletion syndrome with a de novo interstitial 22q13.3 cryptic deletion disrupting SHANK3A Delahaye, A Toutain, A Aboura, et al.
Prenatal Diagnosis|September 6, 2001
Cytogenetic analysis of trophoblasts by comparative genomic hybridization in embryo-fetal development anomaliesA C Tabet, A Aboura, M C Dauge, et al.
Clinical Genetics|March 7, 2018
EFNB2 haploinsufficiency causes a syndromic neurodevelopmental disorderJ Lévy, D Haye, N Marziliano, et al.
Clinical Genetics|May 11, 2011
3D position of pericentromeric heterochromatin within the nucleus of a patient with ICF syndromeC Dupont, F Guimiot, L Perrin, et al.
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.
Clinical Genetics|February 17, 2018
INTU-related oral-facial-digital syndrome type VI: A confirmatory reportA-L Bruel, J Levy, N Elenga, 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.
Prenatal Diagnosis|February 3, 2007
Semilobar holoprosencephaly prenatal diagnosis: an unexpected complex rearrangement in a de novo apparently balanced reciprocal translocation on karyotypeS Kanafani, A Aboura, E Pipiras, et al.
Pageof 2