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Journal Abstract Search

171 related items for PubMed ID: 21396581

  • 1. 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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  • 2. Maternal uniparental isodisomy and heterodisomy on chromosome 6 encompassing a CUL7 gene mutation causing 3M syndrome.
    Sasaki K, Okamoto N, Kosaki K, Yorifuji T, Shimokawa O, Mishima H, Yoshiura KI, Harada N.
    Clin Genet; 2011 Nov; 80(5):478-83. PubMed ID: 21166787
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  • 6. Further expanding the mutational spectrum and investigation of genotype-phenotype correlation in 3M syndrome.
    Simsek-Kiper PO, Taskiran E, Kosukcu C, Arslan UE, Cormier-Daire V, Gonc N, Ozon A, Alikasifoglu A, Kandemir N, Utine GE, Alanay Y, Alikasifoglu M, Boduroglu K.
    Am J Med Genet A; 2019 Jul; 179(7):1157-1172. PubMed ID: 30980518
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  • 7. 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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  • 10. 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 Apr; 76(6):369-78. PubMed ID: 22156540
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  • 14. 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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  • 18. 3M syndrome: an easily recognizable yet underdiagnosed cause of proportionate short stature.
    Al-Dosari MS, Al-Shammari M, Shaheen R, Faqeih E, Alghofely MA, Boukai A, Alkuraya FS.
    J Pediatr; 2012 Jul; 161(1):139-45.e1. PubMed ID: 22325252
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