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Journal Abstract Search

142 related items for PubMed ID: 3220717

  • 1. A unique association of Marfan syndrome with craniofacial hypoplasia, oligophrenia and severe microphthalmia.
    Capocchi G, Fausti R, Zamponini M, Caputo N, Rossi A.
    Ital J Neurol Sci; 1988 Aug; 9(4):397-400. PubMed ID: 3220717
    [Abstract] [Full Text] [Related]

  • 2. Craniofacial aspects of the Marfan syndrome.
    Poole AE.
    Birth Defects Orig Artic Ser; 1989 Aug; 25(4):73-81. PubMed ID: 2697384
    [No Abstract] [Full Text] [Related]

  • 3. The Greig polysyndactyly-craniofacial dysmorphism syndrome.
    Fryns JP, Coeck W, van den Berghe H.
    Eur J Pediatr; 1977 Nov 04; 126(4):283-7. PubMed ID: 201464
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  • 4. Radiographic findings in Shprintzen-Goldberg syndrome.
    Nishimura G, Nagai T.
    Pediatr Radiol; 1996 Nov 04; 26(11):775-8. PubMed ID: 8929375
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  • 5. Cranio-facial dysmorphism with digital abnormalities, oligophrenia and neurological disturbances--a variant of the Freeman-Sheldon syndrome?
    Predescu V, Christodorescu D, Sîrbu C, Ionescu R.
    Neurol Psychiatr (Bucur); 1975 Nov 04; 13(2):127-32. PubMed ID: 810879
    [No Abstract] [Full Text] [Related]

  • 6. The marfan skull.
    Beals RK, Mason L.
    Radiology; 1981 Sep 04; 140(3):723-5. PubMed ID: 7280241
    [Abstract] [Full Text] [Related]

  • 7. [The dentomaxillofacial characteristics of the Prader-Labhart-Willi syndrome. A clinical case report].
    Bassarelli V, Baccetti T, Bassarelli T, Franchi L.
    Minerva Stomatol; 1991 Dec 04; 40(12):811-9. PubMed ID: 1815131
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  • 10. The radiology of Coffin-Lowry syndrome.
    Padley S, Hodgson SV, Sherwood T.
    Br J Radiol; 1990 Jan 04; 63(745):72-5. PubMed ID: 2306591
    [No Abstract] [Full Text] [Related]

  • 11. Vascular pathogenesis of unilateral craniofacial defects.
    Robinson LK, Hoyme HE, Edwards DK, Jones KL.
    J Pediatr; 1987 Aug 04; 111(2):236-9. PubMed ID: 3612395
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  • 13. A new X linked syndrome with mental retardation and craniofacial dysmorphism?
    Hyde-Forster I, McCarthy G, Berry AC.
    J Med Genet; 1992 Oct 04; 29(10):736-8. PubMed ID: 1433236
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  • 17. Mental retardation, macrocephaly, short stature and craniofacial dysmorphism in three sisters. A new entity among the mental retardation-macrocephaly syndromes?
    Fryns JP, Dereymaeker AM, Haegeman J, van den Berghe H.
    Clin Genet; 1988 Apr 04; 33(4):293-8. PubMed ID: 3359686
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  • 18. How wide is the clinical spectrum of the acrocallosal syndrome? Report of a mild case.
    Turolla L, Clementi M, Tenconi R.
    J Med Genet; 1990 Aug 04; 27(8):516-8. PubMed ID: 2103730
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  • 19. Mental retardation, craniofacial dysmorphism, hypogonadism, diabetes mellitus and epilepsy in four siblings. A "new" mental retardation syndrome.
    Fryns JP, Vogels A, van den Berghe H.
    Clin Genet; 1990 Feb 04; 37(2):111-6. PubMed ID: 2107046
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  • 20. Mental retardation, distinct craniofacial dysmorphism, and central nervous system malformation: confirmation of a syndrome.
    Devriendt K, D'Espallier L, Fryns JP.
    J Med Genet; 1996 Mar 04; 33(3):224-6. PubMed ID: 8728696
    [Abstract] [Full Text] [Related]

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