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Index « MedMesh.i » - entrée « Comparative Genomic Hybridization »
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Comorbidity < Comparative Genomic Hybridization < Compartment Syndromes  Facettes :

List of bibliographic references

Number of relevant bibliographic references: 4.
Ident.Authors (with country if any)Title
000A66 (2016) Jessie Mcclelland [Australie] ; Bronwyn Burgess [Australie] ; Patricia Crock [Australie] ; Himanshu Goel [Australie]Sotos syndrome: An unusual presentation with intrauterine growth restriction, generalized lymphedema, and intention tremor.
001556 (2014) Ellyze Van Asbeck [États-Unis] ; Arivudainambi Ramalingam ; Chris Dvorak ; Tian-Jian Chen ; Eva MoravaDuplication at Xq28 involving IKBKG is associated with progressive macrocephaly, recurrent infections, ectodermal dysplasia, benign tumors, and neuropathy.
001700 (2014) Sara M. Sarasua ; Luigi Boccuto ; Julia L. Sharp ; Alka Dwivedi ; Chin-Fu Chen ; Jonathan D. Rollins ; R Curtis Rogers ; Katy Phelan ; Barbara R. DupontClinical and genomic evaluation of 201 patients with Phelan-McDermid syndrome.
002244 (2012) Antoine Italiano [États-Unis] ; Rachael Thomas ; Matthew Breen ; Lei Zhang ; Aimee M. Crago ; Samuel Singer ; Raya Khanin ; Robert G. Maki ; Aleksandra Mihailovic ; Markus Hafner ; Tom Tuschl ; Cristina R. AntonescuThe miR-17-92 cluster and its target THBS1 are differentially expressed in angiosarcomas dependent on MYC amplification.

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