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Journal Abstract Search

265 related items for PubMed ID: 998829

  • 1. Frontometaphyseal dysplasia: evidence for autosomal dominant inheritance.
    Kassner EG, Haller JO, Reddy VH, Mitarotundo A, Katz I.
    AJR Am J Roentgenol; 1976 Dec; 127(6):927-33. PubMed ID: 998829
    [Abstract] [Full Text] [Related]

  • 2. Frontometaphyseal Dysplasia. Evidence for dominant inheritance.
    Weiss L, Reynolds WA, Szymanowski RT.
    Am J Dis Child; 1976 Mar; 130(3):259-61. PubMed ID: 1258835
    [Abstract] [Full Text] [Related]

  • 3. Frontometaphyseal dysplasia: neonatal radiographic diagnosis.
    Glass RB, Rosenbaum KN.
    Am J Med Genet; 1995 May 22; 57(1):1-5. PubMed ID: 7645585
    [Abstract] [Full Text] [Related]

  • 4. Clinical and genetic heterogeneity in frontometaphyseal dysplasia: severe progressive scoliosis in two families.
    Morava E, Illés T, Weisenbach J, Kárteszi J, Kosztolányi G.
    Am J Med Genet A; 2003 Jan 30; 116A(3):272-7. PubMed ID: 12503106
    [Abstract] [Full Text] [Related]

  • 5. Radiology of the autosomal dominant form of craniometaphyseal dysplasia.
    Spiro PC, Hamersma H, Beighton P.
    S Afr Med J; 1975 May 17; 49(21):839-42. PubMed ID: 1135718
    [Abstract] [Full Text] [Related]

  • 6. [Gorlin-Cohen syndrome (frontometaphyseal dysplasia)].
    Kleinsorge H, Böttger E.
    Rofo; 1977 Nov 17; 127(5):451-8. PubMed ID: 144680
    [Abstract] [Full Text] [Related]

  • 7. Familial frontometaphyseal dysplasia- evidence for dominant inheritance.
    Weiss L, Reynolds WA, Szymanowski RT.
    Birth Defects Orig Artic Ser; 1975 Nov 17; 11(5):55-6. PubMed ID: 1218235
    [No Abstract] [Full Text] [Related]

  • 8. [Sex-linked inheritance in fronto-metaphyseal dysplasia].
    Balestrazzi P.
    J Genet Hum; 1985 Dec 17; 33(5):419-25. PubMed ID: 4093771
    [Abstract] [Full Text] [Related]

  • 9. Radiographic findings in Shprintzen-Goldberg syndrome.
    Nishimura G, Nagai T.
    Pediatr Radiol; 1996 Nov 17; 26(11):775-8. PubMed ID: 8929375
    [Abstract] [Full Text] [Related]

  • 10. A new skeletal dysplasia syndrome with dwarfism, craniofacial anomalies, and unique radiographic findings.
    Jones KL, Jones KL, Miller K.
    Am J Med Genet; 1986 Mar 17; 23(3):751-7. PubMed ID: 2420178
    [Abstract] [Full Text] [Related]

  • 11. Frontometaphyseal dysplasia: autosomal dominant or X-linked?
    Beighton P, Hamersma H.
    J Med Genet; 1980 Feb 17; 17(1):53-6. PubMed ID: 7189217
    [Abstract] [Full Text] [Related]

  • 12. Frontometaphyseal dysplasia with congenital urinary tract malformations.
    Kanemura T, Orii T, Ohtani M.
    Clin Genet; 1979 Dec 17; 16(6):399-404. PubMed ID: 527247
    [Abstract] [Full Text] [Related]

  • 13. Radiological changes of frontometaphyseal dysplasia in the neonate.
    Nishimura G, Takano H, Aihara T, Ohashi H, Fukushima Y, Satoh M.
    Pediatr Radiol; 1995 Nov 17; 25 Suppl 1():S143-6. PubMed ID: 8577509
    [Abstract] [Full Text] [Related]

  • 14. [Cranial metaphysial dysplasia (Jackson) (author's transl)].
    Wemmer U, Böttger E.
    Rofo; 1978 Jan 17; 128(1):66-9. PubMed ID: 146664
    [Abstract] [Full Text] [Related]

  • 15. [Doughnut lesions of the cranial vault: an hereditary bone dysplasia].
    Aubé L, Vallières M, Lemay M.
    Can Assoc Radiol J; 1988 Sep 17; 39(3):204-8. PubMed ID: 2971055
    [Abstract] [Full Text] [Related]

  • 16. Frontometaphyseal dysplasia.
    Holt JF, Thompson GR, Arenberg IK.
    Radiol Clin North Am; 1972 Aug 17; 10(2):225-43. PubMed ID: 5044403
    [No Abstract] [Full Text] [Related]

  • 17. Frontometaphyseal dysplasia 1 in a patient from Sri Lanka.
    Dissanayake R, Senanayake MP, Fernando J, Robertson SP, Dissanayake VHW, Sirisena ND.
    Am J Med Genet A; 2021 Apr 17; 185(4):1317-1320. PubMed ID: 33372358
    [Abstract] [Full Text] [Related]

  • 18. Skeletal dysplasia syndrome with progeroid appearance, characteristic facial and limb anomalies, multiple synostoses, and distinct skeletal changes: a variant example of the Lenz-Majewski syndrome.
    Chrzanowska KH, Fryns JP, Krajewska-Walasek M, Van den Berghe H, Wisniewski L.
    Am J Med Genet; 1989 Apr 17; 32(4):470-4. PubMed ID: 2773987
    [Abstract] [Full Text] [Related]

  • 19. Craniometaphyseal dysplasia--variability of expression within a large family.
    Beighton P, Hamersma H, Horan F.
    Clin Genet; 1979 Mar 17; 15(3):252-8. PubMed ID: 421364
    [Abstract] [Full Text] [Related]

  • 20. Frontometaphyseal dysplasia: symptoms and possible mode of inheritance.
    Jend-Rossmann I, Jend HH, Ringe JD, Gundlach KK.
    J Oral Maxillofac Surg; 1984 Nov 17; 42(11):743-8. PubMed ID: 6593448
    [Abstract] [Full Text] [Related]

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