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Phenotypical characterization of 13q deletion syndrome: Report of two cases
Patients with 13q deletion syndrome are characterized with different phenotypical features depending on the size and location of the deleted region on chromosome 13. These patients fall into three groups: In Group 1, deleted region is in the proximal and does not extend into q32; in Group 2, deleted...
Tallennettuna:
| Julkaisussa: | Indian J Hum Genet |
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| Päätekijät: | , , , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
Medknow Publications & Media Pvt Ltd
2014
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4228577/ https://ncbi.nlm.nih.gov/pubmed/25400354 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/0971-6866.142912 |
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