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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

75 related items for PubMed ID: 517478

  • 1. Cranioectodermal dysplasia.
    Gellis S, Feingold M, Dubner D.
    Am J Dis Child; 1979 Dec; 133(12):1275-6. PubMed ID: 517478
    [No Abstract] [Full Text] [Related]

  • 2. Undiagnosed syndrome of psychomotor retardation, low birthweight dwarfism, skeletal, dental, dermal and genital anomalies.
    Elliott DE.
    Birth Defects Orig Artic Ser; 1975 Dec; 11(2):364-7. PubMed ID: 1241660
    [No Abstract] [Full Text] [Related]

  • 3. Proceedings: Craniocarpotarsal dysplasia with partial mandibular agenesis--an embryologic rarity or unusual gene expression?
    Sanger RG.
    Birth Defects Orig Artic Ser; 1976 Dec; 12(5):331-2. PubMed ID: 953240
    [No Abstract] [Full Text] [Related]

  • 4. Tricho-dento-osseous syndrome: heterogeneity or clinical variability.
    Shapiro SD, Quattromani FL, Jorgenson RJ, Young RS.
    Am J Med Genet; 1983 Oct; 16(2):225-36. PubMed ID: 6650567
    [Abstract] [Full Text] [Related]

  • 5. [The Silver-Russell syndrome].
    Bene M, Moga L.
    Rev Pediatr Obstet Ginecol Pediatr; 1980 Oct; 29(3):255-63. PubMed ID: 6781034
    [No Abstract] [Full Text] [Related]

  • 6. Frontometaphyseal dysplasia: a progressive disease of bone and connective tissue.
    Danks DM, Mayne V.
    Birth Defects Orig Artic Ser; 1974 Oct; 10(12):57-60. PubMed ID: 4282264
    [No Abstract] [Full Text] [Related]

  • 7. The KBG syndrome-a syndrome of short stature, characteristic facies, mental retardation, macrodontia and skeletal anomalies.
    Herrmann J, Pallister PD, Tiddy W, Opitz JM.
    Birth Defects Orig Artic Ser; 1975 Oct; 11(5):7-18. PubMed ID: 1218237
    [No Abstract] [Full Text] [Related]

  • 8. Otolaryngological disorders in craniometaphyseal dysplasia.
    Kietzer G, Paparella MM.
    Laryngoscope; 1969 May; 79(5):921-41. PubMed ID: 5770043
    [No Abstract] [Full Text] [Related]

  • 9. [Cohen syndrome: report of two cases in female twins].
    Arcas Martínez J, García Peñas JJ, Ramos Lizana J, Díaz González C, Pascual Castroviejo I.
    An Esp Pediatr; 1991 Jan; 34(1):83-5. PubMed ID: 2018266
    [No Abstract] [Full Text] [Related]

  • 10. [Congenital atrichia associated with keratin cysts - Variant of partial ectodermal dysplasia].
    Czarnecki N, Stingl G.
    Z Hautkr; 1980 Feb 15; 55(4):210-7. PubMed ID: 7405339
    [Abstract] [Full Text] [Related]

  • 11. Teschler-Nicola/Killian syndrome: a sporadic case in an 11-year-old male.
    Hall BD.
    J Clin Dysmorphol; 1983 Feb 15; 1(3):14-7. PubMed ID: 6584555
    [No Abstract] [Full Text] [Related]

  • 12. [Sex-linked inheritance in fronto-metaphyseal dysplasia].
    Balestrazzi P.
    J Genet Hum; 1985 Dec 15; 33(5):419-25. PubMed ID: 4093771
    [Abstract] [Full Text] [Related]

  • 13. Abnormal hair, craniofacial dysmorphism, and severe mental retardation - a new syndrome?
    Killian W, Zonana J, Schroer RJ.
    J Clin Dysmorphol; 1983 Dec 15; 1(3):6-13. PubMed ID: 6584560
    [No Abstract] [Full Text] [Related]

  • 14. [Skeletal anomalies of the hand, skull, and spine in a group of 15 children with Turner's syndrome].
    Kuklík M, Klán Z, Holík F.
    Cesk Pediatr; 1980 Oct 15; 35(10):529-31. PubMed ID: 7438264
    [No Abstract] [Full Text] [Related]

  • 15. [The Roberts-SC phocomelia syndrome. Apropos of a case without cytogenetic changes and review of the literature].
    López-Herce J, Rodríguez Sánchez C, Duelo M, Fontoura M, González M, Gracia R, Oliver A, Peralta A.
    An Esp Pediatr; 1985 Dec 15; 23(8):588-92. PubMed ID: 3006564
    [No Abstract] [Full Text] [Related]

  • 16. Generalized osseous abnormalities in the Marshall syndrome.
    O'Donnell JJ, Sirkin S, Hall BD.
    Birth Defects Orig Artic Ser; 1976 Dec 15; 12(5):299-314. PubMed ID: 953235
    [No Abstract] [Full Text] [Related]

  • 17. Syndrome identification case report 90: multiple craniofacial and skeletal defects.
    Mastroiacovo P, De Rosa G, Satta MA, Colavita N, Priolo F, Pasargiklian E.
    J Clin Dysmorphol; 1983 Dec 15; 1(1):13-5. PubMed ID: 6580383
    [No Abstract] [Full Text] [Related]

  • 18. A syndrome of hemimaxillary enlargement, asymmetry of the face, tooth abnormalities, and skin findings (HATS).
    Welsch MJ, Stein SL.
    Pediatr Dermatol; 2004 Dec 15; 21(4):448-51. PubMed ID: 15283787
    [Abstract] [Full Text] [Related]

  • 19. Clinical features of tricho-dento-osseous syndrome and presentation of three new cases: an addition to clinical heterogeneity.
    Islam M, Lurie AG, Reichenberger E.
    Oral Surg Oral Med Oral Pathol Oral Radiol Endod; 2005 Dec 15; 100(6):736-42. PubMed ID: 16301156
    [Abstract] [Full Text] [Related]

  • 20. New syndrome of skeletal, dental and hair anomalies.
    Sensenbrenner JA, Dorst JP, Owens RP.
    Birth Defects Orig Artic Ser; 1975 Dec 15; 11(2):372-9. PubMed ID: 1227553
    [Abstract] [Full Text] [Related]

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