Microarray Analysis of 8p23.1 Deletion in New Patients with Atypical Phenotypical Traits

We describe two patients carrying deletions of chromosome 8p23.1 with a commonly critical region identified by means of oligonucleotide array comparative genomic hybridization (array CGH). They didn't present congenital heart defects or behavioral problems. Only one patient presented with intel...

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Bibliografiset tiedot
Julkaisussa:J Pediatr Genet
Päätekijät: Khelifa, Hela Ben, Kammoun, Molka, Hannachi, Hanene, Soyah, Najla, Hammami, Saber, Elghezal, Hatem, Sanlaville, Damien, Saad, Ali, Mougou-Zerelli, Soumaya
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: Georg Thieme Verlag KG 2015
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC4906530/
https://ncbi.nlm.nih.gov/pubmed/27617130
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1055/s-0035-1565269
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