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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 [Abstract] [Full Text] [Related]
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 [Abstract] [Full Text] [Related]
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 [Abstract] [Full Text] [Related]
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 [Abstract] [Full Text] [Related]
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 [Abstract] [Full Text] [Related]
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 [Abstract] [Full Text] [Related]
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 [Abstract] [Full Text] [Related]