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New insights into the pathogenesis of Beckwith-Wiedemann an..:
Demars, Julie
;
Rossignol, Sylvie
;
Netchine, Irène
...
info:eu-repo/semantics/altIdentifier/doi/10.1002/humu.21558. , 2011
Link:
https://inserm.hal.science/inserm-00610827
RT Journal T1
New insights into the pathogenesis of Beckwith-Wiedemann and Silver-Russell syndromes: contribution of small copy number variations to 11p15 imprinting defects
UL https://suche.suub.uni-bremen.de/peid=base-ftunivrennes1hal:oai:HAL:inserm-00610827v1&Exemplar=1&LAN=DE A1 Demars, Julie A1 Rossignol, Sylvie A1 Netchine, Irène A1 Syin Lee, Kai A1 Shmela, Mansur A1 Faivre, Laurence A1 Weill, Jacques A1 Odent, Sylvie A1 Azzi, Salah A1 Callier, Patrick A1 Lucas, Josette A1 Dubourg, Christèle A1 Andrieux, Joris A1 Le Bouc, Yves A1 El-Osta, Assam A1 Gicquel, Christine PB HAL CCSD; Wiley YR 2011 K1 fetal growth K1 genomic imprinting K1 copy number variation K1 11p15 region K1 Silver-Russell syndrome K1 Beckwith-Wiedemann syndrome K1 MESH: Base Sequence K1 MESH: Male K1 MESH: Pedigree K1 MESH: Polymorphism K1 Single Nucleotide K1 MESH: Silver-Russell Syndrome K1 MESH: Adult K1 MESH: Beckwith-Wiedemann Syndrome K1 MESH: Chromosomes K1 Human K1 Pair 11 K1 MESH: Comparative Genomic Hybridization K1 MESH: DNA Copy Number Variations K1 MESH: DNA Methylation K1 MESH: Female K1 MESH: Genomic Imprinting K1 MESH: Humans K1 [SDV.GEN]Life Sciences [q-bio]/Genetics K1 [SDV.BDD]Life Sciences [q-bio]/Development Biology JF info:eu-repo/semantics/altIdentifier/doi/10.1002/humu.21558 LK http://dx.doi.org/https://inserm.hal.science/inserm-00610827 DO https://inserm.hal.science/inserm-00610827 SF ELIB - SuUB Bremen
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