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PUBMED FOR HANDHELDS

Journal Abstract Search


178 related items for PubMed ID: 4220009

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  • 23. The EEC syndrome. Report of six patients.
    Pashayan HM, Pruzansky S, Solomon L.
    Birth Defects Orig Artic Ser; 1974; 10(7):105-27. PubMed ID: 4425508
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  • 27. Ectrodactyly, ectodermal dysplasia, and clefting syndrome.
    Kaiser-Kupfer M.
    Am J Ophthalmol; 1973 Dec; 76(6):992-8. PubMed ID: 4759861
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  • 33. Oral manifestations of systemic genetic disorders. 3.
    Gorlin RJ, Sedano HO.
    Postgrad Med; 1971 Mar; 49(3):155-8. PubMed ID: 4993998
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  • 34. Hereditary childhood hearing loss and integumentary system disease.
    Konigsmark BW.
    J Pediatr; 1972 Jun; 80(6):909-19. PubMed ID: 5026034
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  • 36. Tricho-rhino-phalangeal syndrome type III.
    Kajii T, Fernandez Gonzalez I, Matsuura S.
    Am J Med Genet; 1994 Feb 01; 49(3):349-50. PubMed ID: 8209900
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  • 37. [A dominant syndrome associated with polysyndactyly, spatule thumb, facial abnormalities, and mental retardation. (A particular form of Noack's acrocephalosyndactylia)].
    Gnamey D, Farriaux JP.
    J Genet Hum; 1971 Dec 01; 19(4):299-316. PubMed ID: 5152131
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  • 39. N--variable expressivity in craniocarpotarsal dysplasia.
    Wilson CD, Pearce WG.
    Birth Defects Orig Artic Ser; 1974 Dec 01; 10(5):243-8. PubMed ID: 4220007
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