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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

140 related items for PubMed ID: 7468656

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  • 24. Autosomal dominant inheritance of tibial meromelia. Report of a kindred.
    Clark MW.
    J Bone Joint Surg Am; 1975 Mar; 57(2):262-4. PubMed ID: 1112852
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  • 27. Femoral hypoplasia-unusual facies syndrome with bifid hallux, absent tibia, and macrophallus: a report of a Bedouin baby.
    Sabry MA, Obenbergerova D, Al-Sawan R, Saleh QA, Farah S, Al-Awadi SA, Farag TI.
    J Med Genet; 1996 Feb; 33(2):165-7. PubMed ID: 8929957
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  • 29. Through-knee amputation for a patient with proximal femur focal deficiency and tibial hemimelia: surgical anatomy and clinical implications.
    Lloyd S, Rashid AH, Das S, Ibrahim S.
    Anat Sci Int; 2014 Mar; 89(2):122-5. PubMed ID: 24158808
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  • 32. Familial broad terminal phalanges with one individual showing additional anomalies.
    Pavone L, Sorge G, Pavone V, Rizzo R, Ruggieri M, Polizzi A, Opitz JM.
    Am J Med Genet; 1997 Aug 22; 71(3):271-4. PubMed ID: 9268094
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  • 33. Six generations of a family with multiple limb deficiencies.
    Helal A, Perry T, Ogden JA, Greene TL.
    J Pediatr Orthop; 1993 Aug 22; 13(2):210-3. PubMed ID: 8459013
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  • 34. Ulnar/fibular ray defect and brachydactyly in a family: a possible new autosomal dominant syndrome.
    Morava E, Czakó M, Kárteszi J, Cser B, Weissbecker K, Méhes K.
    Clin Dysmorphol; 2003 Jul 22; 12(3):161-5. PubMed ID: 14564152
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  • 36. Two sporadic cases of amelia/phocomelia with similar phenotype: rare and unusually symmetrical form of FFU dysostosis or separate entity?
    Kardon NB, Dana LP, FitzGerald JM, Opitz JM.
    Am J Med Genet Suppl; 1986 Jul 22; 2():239-45. PubMed ID: 3146295
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  • 39. Femur-fibula-ulna complex.
    Furness J, Henman P, Sturgiss S.
    Arch Dis Child Fetal Neonatal Ed; 2013 Nov 22; 98(6):F479. PubMed ID: 23645575
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