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Journal Abstract Search

201 related items for PubMed ID: 33783941

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  • 9. Further delineation of the Van den Ende-Gupta syndrome.
    Ali R, Almureikhi M, Al-Musaifri F, Bhat V, Teebi A, Ben-Omran T.
    Am J Med Genet A; 2010 Dec; 152A(12):3095-100. PubMed ID: 21108395
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  • 10. van den Ende-Gupta syndrome of blepharophimosis, arachnodactyly, and congenital contractures.
    Guerra D, Sanchez O, Richieri-Costa A.
    Am J Med Genet A; 2005 Aug 01; 136A(4):377-80. PubMed ID: 15971261
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  • 11. Unmasking of a Recessive SCARF2 Mutation by a 22q11.12 de novo Deletion in a Patient with Van den Ende-Gupta Syndrome.
    Bedeschi MF, Colombo L, Mari F, Hofmann K, Rauch A, Gentilin B, Renieri A, Clerici D.
    Mol Syndromol; 2010 Aug 01; 1(5):239-245. PubMed ID: 22140376
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  • 13. Expanding the clinical spectrum and allelic heterogeneity in van den Ende-Gupta syndrome.
    Patel N, Salih MA, Alshammari MJ, Abdulwahhab F, Adly N, Alzahrani F, Elgamal EA, Elkhashab HY, Al-Qattan M, Alkuraya FS.
    Clin Genet; 2014 May 01; 85(5):492-4. PubMed ID: 23808541
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  • 14. Identification of a novel variant of SCARF2 in a Jordanian family with a van den Ende-Gupta Syndrome and literature review.
    Odeh O, Barqawi T, Rashid H, Almashhdi S, Shboul M.
    Clin Dysmorphol; 2022 Jul 01; 31(3):157-161. PubMed ID: 35256560
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  • 17. Exploring scavenger receptor class F member 2 and the importance of scavenger receptor family in prediagnostic diseases.
    Vo TT, Kong G, Kim C, Juang U, Gwon S, Jung W, Nguyen H, Kim SH, Park J.
    Toxicol Res; 2023 Jul 01; 39(3):341-353. PubMed ID: 37398563
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