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PUBMED FOR HANDHELDS

Journal Abstract Search


132 related items for PubMed ID: 35150935

  • 1. 3M syndrome: A Tunisian seven-cases series.
    Khachnaoui-Zaafrane K, Ouertani I, Zanati A, Kandara H, Maazoul F, Mrad R.
    Eur J Med Genet; 2022 Mar; 65(3):104448. PubMed ID: 35150935
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  • 2. Natural history of facial and skeletal features from neonatal period to adulthood in a 3M syndrome cohort with biallelic CUL7 or OBSL1 variants.
    Tüysüz B, Alp Ünkar Z, Turan H, Gezdirici A, Uludağ Alkaya D, Kasap B, Yeşil G, Vural M, Ercan O.
    Eur J Med Genet; 2021 Dec; 64(12):104346. PubMed ID: 34597859
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  • 3. Exploring the spectrum of 3-M syndrome, a primordial short stature disorder of disrupted ubiquitination.
    Clayton PE, Hanson D, Magee L, Murray PG, Saunders E, Abu-Amero SN, Moore GE, Black GC.
    Clin Endocrinol (Oxf); 2012 Sep; 77(3):335-42. PubMed ID: 22624670
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  • 4. A rare cause of syndromic short stature: 3M syndrome in three families.
    Isik E, Arican D, Atik T, Ooi JE, Darcan S, Ozen S, Simsek Kiper PO, Utine E, Cogulu O, Ozkinay F.
    Am J Med Genet A; 2021 Feb; 185(2):461-468. PubMed ID: 33258289
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  • 6. The 3M syndrome.
    Huber C, Munnich A, Cormier-Daire V.
    Best Pract Res Clin Endocrinol Metab; 2011 Feb; 25(1):143-51. PubMed ID: 21396581
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  • 9. Prenatal diagnosis and preimplantation genetics testing of 3M syndrome in a Chinese family with novel biallelic variants of CUL7.
    Wang X, He Y, Wang X, Kong X, Lin Y, Yao Y, Huang Y.
    Mol Genet Genomic Med; 2024 Jan; 12(1):e2284. PubMed ID: 37877343
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  • 14. Pre- and post-natal growth in two sisters with 3-M syndrome.
    Lugli L, Bertucci E, Mazza V, Elmakky A, Ferrari F, Neuhaus C, Percesepe A.
    Eur J Med Genet; 2016 Apr; 59(4):232-6. PubMed ID: 26850509
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  • 15. Novel mutation in Cul7 gene in a family diagnosed with 3M syndrome.
    Shaikh S, Shettigar SKG, Kumar S, Kantharia S, Kurva J, Cherian S.
    J Genet; 2019 Mar; 98():. PubMed ID: 30945686
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  • 18. The genetics of 3-M syndrome: unravelling a potential new regulatory growth pathway.
    Hanson D, Murray PG, Black GC, Clayton PE.
    Horm Res Paediatr; 2011 Mar; 76(6):369-78. PubMed ID: 22156540
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