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PUBMED FOR HANDHELDS

Journal Abstract Search


147 related items for PubMed ID: 3442298

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  • 2. Facial dysmorphology, roentgenographic measurements, and clinical genetics.
    Saksena SS, Bader P, Bixler D.
    J Craniofac Genet Dev Biol; 1989; 9(1):29-43. PubMed ID: 2794000
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  • 5. Anthropometric craniofacial pattern profiles in Down syndrome.
    Allanson JE, O'Hara P, Farkas LG, Nair RC.
    Am J Med Genet; 1993 Oct 01; 47(5):748-52. PubMed ID: 8267006
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  • 6. Craniofacial anthropometric pattern profile in hypohidrotic ectodermal dysplasia--application in detection of gene carriers.
    Skrinjarić I, Skrinjarić K, Vranić DN, Majstorović M, Glavina D.
    Coll Antropol; 2003 Dec 01; 27(2):753-9. PubMed ID: 14746168
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  • 10. Craniofacial anomalies, abnormal hair, camptodactyly, and caudal appendage (Teebi-Shaltout syndrome): clinical and autopsy findings.
    Froster UG, Rehder H, Höhn W, Oberheuser F.
    Am J Med Genet; 1993 Oct 01; 47(5):717-22. PubMed ID: 8267003
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  • 11. Familial occurrence of renal and Müllerian duct hypoplasia, craniofacial anomalies, severe growth and developmental delay.
    Davee MA, Moore CA, Bull MJ, Hodes ME.
    Am J Med Genet; 1992 Oct 01; 44(3):293-6. PubMed ID: 1283287
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  • 15. Teebi hypertelorism syndrome: report of a third family.
    Toriello HV, Delp K.
    Clin Dysmorphol; 1994 Oct 01; 3(4):335-9. PubMed ID: 7894738
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  • 16. Previously undescribed syndrome of craniofacial, hand anomalies, and sensorineural deafness.
    Sommer A, Young-Wee T, Frye T.
    Am J Med Genet; 1983 May 01; 15(1):71-7. PubMed ID: 6859126
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  • 17. Maxillonasal dysplasia (Binder's syndrome). A study of craniofacial morphology, associated malformations and familial relations.
    Olow-Nordenram M.
    Swed Dent J Suppl; 1987 May 01; 47():1-38. PubMed ID: 3499673
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