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Expert Review of Molecular Diagnostics
|
June 29, 2011
Oligonucleotide microarrays in constitutional genetic diagnosis
Boris 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 phenotype
Bertrand Isidor, Sophie Guillard, Antoine Hamel, et al.
Annales De Genetique
|
September 1, 2004
Inherited ring chromosome 8 without loss of subtelomeric sequences
Cedric 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 growth
Cedric 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 patient
Cedric 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 Disorders
Marie 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 anomalies
Bertrand 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 syndrome
Franck Bourdeaut, Bertrand Isidor, Sandrine Ferrand, et al.
American Journal of Medical Genetics. Part A
|
April 29, 2018
Familial autosomal dominant severe ankyloglossia with tooth abnormalities
Anaëlle Lenormand, Roman Khonsari, Pierre Corre, et al.
Nucleic Acids Research
|
May 16, 2006
Single-cell chromosomal imbalances detection by array CGH
Cedric Le Caignec, Claudia Spits, Karen Sermon, et al.
Page
of 4
Search research articles
Search
Showing results (1-10 of 37) with videos related to
Sort By:
Page
of 4
Expert Review of Molecular Diagnostics
|
June 29, 2011
Oligonucleotide microarrays in constitutional genetic diagnosis
Boris 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 phenotype
Bertrand Isidor, Sophie Guillard, Antoine Hamel, et al.
Annales De Genetique
|
September 1, 2004
Inherited ring chromosome 8 without loss of subtelomeric sequences
Cedric 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 growth
Cedric 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 patient
Cedric 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 Disorders
Marie 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 anomalies
Bertrand 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 syndrome
Franck Bourdeaut, Bertrand Isidor, Sandrine Ferrand, et al.
American Journal of Medical Genetics. Part A
|
April 29, 2018
Familial autosomal dominant severe ankyloglossia with tooth abnormalities
Anaëlle Lenormand, Roman Khonsari, Pierre Corre, et al.
Nucleic Acids Research
|
May 16, 2006
Single-cell chromosomal imbalances detection by array CGH
Cedric Le Caignec, Claudia Spits, Karen Sermon, et al.
Page
of 4