Result Number | Material Type | Add to My Shelf Action | Record Details and Options |
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1 |
Material Type: Report
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Craniolacunia in A neonate; A clinical and CT scan illustrative case reportEdzie, Emmanuel Kobina Mesi ; Dzefi-Tettey, Klenam ; Gorleku, Philip Narteh ; Agyen-Mensah, Kwasi ; Kusodzi, Henry ; Quarshie, Frank ; Asemah, Abdul RamanClinical case reports, 2021, Vol.9 (7), p.e04501-e04501Texto completo disponível |
2 |
Material Type: Report
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Severe retinal complications in Knobloch Syndrome - Three siblings without clinically apparent occipital defects and a review of the literatureArepalli, Sruthi ; DeBenedictis, Meghan M. ; Yuan, Alex ; Traboulsi, Elias I.Ophthalmic Genetics, 2022, Vol.43 (3), p.362-370Taylor & FrancisTexto completo disponível |
3 |
Material Type: Report
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Whole genome sequencing in a Knobloch syndrome family confirms the molecular diagnosisPatel, Chetan Khantibai ; Broadgate, Suzanne ; Shalaby, Ahmed ; Yu, Jing ; Nemeth, Andrea H. ; Downes, Susan M ; Halford, StephanieOphthalmic Genetics, 2022, Vol.43 (2), p.201-209Taylor & FrancisTexto completo disponível |
4 |
Material Type: Report
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Myopia-The future progression of myopia: Seeing where we are goingMackey, David A.Ophthalmic Genetics, 2016, Vol.37 (4), p.361-365Taylor & FrancisTexto completo disponível |
5 |
Material Type: Report
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Clonality of neutrophilia associated with plasma cell neoplasms: report of a SETBP1 mutation and analysis of a single institution seriesStevens, Brett ; Maxson, Julia ; Tyner, Jeffrey ; Smith, Clayton A. ; Gutman, Jonathan A. ; Robinson, William ; Jordan, Craig T. ; Lee, Choon-Kee ; Swisshelm, Karen ; Tobin, Jennifer ; Wei, Qi ; Schowinsky, Jeffrey ; Rinella, Sean ; Lee, Hea Gie ; Pollyea, Daniel A.Leukemia & Lymphoma, 2016, Vol.57 (4), p.927-934Taylor & FrancisTexto completo disponível |