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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

111 related items for PubMed ID: 16001436

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  • 7. Coxa vara in chondrodysplasia: prognosis study of 35 hips in 19 children.
    Trigui M, Pannier S, Finidori G, Padovani JP, Glorion C.
    J Pediatr Orthop; 2008 Sep; 28(6):599-606. PubMed ID: 18724194
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  • 11. Frontonasal dysplasia associated with tetralogy of Fallot.
    De Moor MM, Baruch R, Human DG.
    J Med Genet; 1987 Feb; 24(2):107-9. PubMed ID: 3560167
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  • 13. Coxa vara in childhood: evaluation and management.
    Beals RK.
    J Am Acad Orthop Surg; 1998 Feb; 6(2):93-9. PubMed ID: 9682071
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  • 14. Bindewald syndrome: Tetralogy of Fallot, large ears, severe growth and mental retardation.
    Belengeanu V, Rozsnyai K, Farcaş S, Lacatuşu A.
    Am J Med Genet A; 2005 Feb 01; 132A(4):445-6. PubMed ID: 15578610
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  • 17. Infantile coxa vara.
    Pavlov H, Goldman AB, Freiberger RH.
    Radiology; 1980 Jun 01; 135(3):631-40. PubMed ID: 7384448
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  • 18. A case with Pyle type metaphyseal dysplasia: clinical, radiological and histological evaluation.
    Percin EF, Percin S, Koptagel E, Demirel H.
    Genet Couns; 2003 Jun 01; 14(4):387-93. PubMed ID: 14738111
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  • 19. Mutations in Fibronectin Cause a Subtype of Spondylometaphyseal Dysplasia with "Corner Fractures".
    Lee CS, Fu H, Baratang N, Rousseau J, Kumra H, Sutton VR, Niceta M, Ciolfi A, Yamamoto G, Bertola D, Marcelis CL, Lugtenberg D, Bartuli A, Kim C, Hoover-Fong J, Sobreira N, Pauli R, Bacino C, Krakow D, Parboosingh J, Yap P, Kariminejad A, McDonald MT, Aracena MI, Lausch E, Unger S, Superti-Furga A, Lu JT, Baylor-Hopkins Center for Mendelian GenomicsBaylor-Hopkins Center for Mendelian Genomics, Houston, TX 77030, USA., Cohn DH, Tartaglia M, Lee BH, Reinhardt DP, Campeau PM.
    Am J Hum Genet; 2017 Nov 02; 101(5):815-823. PubMed ID: 29100092
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  • 20. Unexpected findings in cervical spine in spondylometaphyseal dysplasia Sutcliff type FN1-related.
    Ramos-Mejía R, Heath KE, Modamio-Høybjør S, Huckstadt V, Calcagni J, Remondino R, Fano V.
    Am J Med Genet A; 2024 Mar 02; 194(3):e63469. PubMed ID: 37940834
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