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Cedric Le Caignec

Showing results (1-10 of 37) with videos related to

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Expert Review of Molecular Diagnostics|June 29, 2011
Oligonucleotide microarrays in constitutional genetic diagnosisBoris Keren, Cedric Le Caignec
American Journal of Medical Genetics. Part A|July 17, 2007
Genochondromatosis type II: report of a new patient and further delineation of the phenotypeBertrand Isidor, Sophie Guillard, Antoine Hamel, et al.
Annales De Genetique|September 1, 2004
Inherited ring chromosome 8 without loss of subtelomeric sequencesCedric Le Caignec, Michelle Boceno, Sebastien Jacquemont, et al.
American Journal of Medical Genetics. Part A|October 16, 2007
Third case of paternal isodisomy for chromosome 7 with cystic fibrosis: a new patient presenting with normal growthCedric Le Caignec, Bertrand Isidor, Ulrika de Pontbriand, et al.
American Journal of Medical Genetics. Part A|October 16, 2007
Complete sex reversal in a WAGR syndrome patientCedric Le Caignec, Capucine Delnatte, Joris R Vermeesch, et al.
American Journal of Respiratory and Critical Care Medicine|June 13, 2019
Clinical, Histopathological, and Molecular Diagnostics in Lethal Lung Developmental DisordersMarie Vincent, Justyna A Karolak, Gail Deutsch, et al.
European Journal of Medical Genetics|February 20, 2008
Inherited 18q23 duplication in a fetus with multiple congenital anomaliesBertrand Isidor, Norbert Winer, Madeleine Joubert, et al.
American Journal of Medical Genetics. Part A|June 15, 2011
Homozygous PTEN deletion in neuroblastoma arising in a child with Cowden syndromeFranck Bourdeaut, Bertrand Isidor, Sandrine Ferrand, et al.
American Journal of Medical Genetics. Part A|April 29, 2018
Familial autosomal dominant severe ankyloglossia with tooth abnormalitiesAnaëlle Lenormand, Roman Khonsari, Pierre Corre, et al.
Nucleic Acids Research|May 16, 2006
Single-cell chromosomal imbalances detection by array CGHCedric Le Caignec, Claudia Spits, Karen Sermon, et al.
Pageof 4

Showing results (1-10 of 37) with videos related to

Sort By:
Pageof 4
Expert Review of Molecular Diagnostics|June 29, 2011
Oligonucleotide microarrays in constitutional genetic diagnosisBoris Keren, Cedric Le Caignec
American Journal of Medical Genetics. Part A|July 17, 2007
Genochondromatosis type II: report of a new patient and further delineation of the phenotypeBertrand Isidor, Sophie Guillard, Antoine Hamel, et al.
Annales De Genetique|September 1, 2004
Inherited ring chromosome 8 without loss of subtelomeric sequencesCedric Le Caignec, Michelle Boceno, Sebastien Jacquemont, et al.
American Journal of Medical Genetics. Part A|October 16, 2007
Third case of paternal isodisomy for chromosome 7 with cystic fibrosis: a new patient presenting with normal growthCedric Le Caignec, Bertrand Isidor, Ulrika de Pontbriand, et al.
American Journal of Medical Genetics. Part A|October 16, 2007
Complete sex reversal in a WAGR syndrome patientCedric Le Caignec, Capucine Delnatte, Joris R Vermeesch, et al.
American Journal of Respiratory and Critical Care Medicine|June 13, 2019
Clinical, Histopathological, and Molecular Diagnostics in Lethal Lung Developmental DisordersMarie Vincent, Justyna A Karolak, Gail Deutsch, et al.
European Journal of Medical Genetics|February 20, 2008
Inherited 18q23 duplication in a fetus with multiple congenital anomaliesBertrand Isidor, Norbert Winer, Madeleine Joubert, et al.
American Journal of Medical Genetics. Part A|June 15, 2011
Homozygous PTEN deletion in neuroblastoma arising in a child with Cowden syndromeFranck Bourdeaut, Bertrand Isidor, Sandrine Ferrand, et al.
American Journal of Medical Genetics. Part A|April 29, 2018
Familial autosomal dominant severe ankyloglossia with tooth abnormalitiesAnaëlle Lenormand, Roman Khonsari, Pierre Corre, et al.
Nucleic Acids Research|May 16, 2006
Single-cell chromosomal imbalances detection by array CGHCedric Le Caignec, Claudia Spits, Karen Sermon, et al.
Pageof 4