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PUBMED FOR HANDHELDS

Journal Abstract Search

118 related items for PubMed ID: 8285473

  • 1.
    ; . PubMed ID:
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  • 3. Multiple lentigines syndrome in a Nigerian family.
    Kubeyinje EP, Onunu AN, Obasohan AO.
    Trop Geogr Med; 1993; 45(3):135-7. PubMed ID: 8362457
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  • 5. [Simpson-Golabi-Behmel syndrome. A new overgrowth syndrome with increased risk of tumor development].
    Weidle B, Orstavik KH.
    Tidsskr Nor Laegeforen; 1998 Apr 20; 118(10):1556-8. PubMed ID: 9615582
    [Abstract] [Full Text] [Related]

  • 6. Linkage studies of four fibrillar collagen genes in three pedigrees with Larsen-like syndrome.
    Bonaventure J, Lasselin C, Mellier J, Cohen-Solal L, Maroteaux P.
    J Med Genet; 1992 Jul 20; 29(7):465-70. PubMed ID: 1640425
    [Abstract] [Full Text] [Related]

  • 7. Leprechaunism (Donohue's syndrome): a case report.
    Tokatli A, Ozsoylu S, Ozme S.
    Turk J Pediatr; 1993 Jul 20; 35(4):319-22. PubMed ID: 8160285
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  • 8. [The lesions associated with leprechaunism (author's transl)].
    Lebreuil G, Pizzi M, Sebaoun M, Oddou JH.
    Arch Anat Cytol Pathol; 1980 Jul 20; 28(5):310-6. PubMed ID: 7447519
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  • 9. [The G syndrome: description of a case/and familial studies].
    Calandi C, Adami-Lami Conti C, Mannini A, Fantacci C, Nistri R, Giovannucci ML.
    Arch De Vecchi Anat Patol; 1980 Jul 20; 64(1):59-73. PubMed ID: 7027970
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  • 10. [Leprechaunism(Donohue syndrome)].
    Morooka K.
    Ryoikibetsu Shokogun Shirizu; 2000 Jul 20; (30 Pt 5):207-8. PubMed ID: 11057198
    [No Abstract] [Full Text] [Related]

  • 11. The MIller-Dieker syndrome.
    Jones KL, Gilbert EF, Kaveggia EG, Opitz JM.
    Pediatrics; 1980 Aug 20; 66(2):277-81. PubMed ID: 7402813
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  • 12. [Hereditary diseases with joint laxity].
    Steinmann B, Gitzelmann R.
    Orthopade; 1984 Jan 20; 13(1):9-18. PubMed ID: 6709362
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  • 13. Growth deficiency, facial dysmorphogenesis and brachydactyly: a new syndrome.
    Frias JL, Guttery EG, Felman AH.
    Birth Defects Orig Artic Ser; 1975 Jan 20; 11(2):30-3. PubMed ID: 1227535
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  • 14. Familial deficiency of growth hormone and spinal muscular atrophy.
    Leroy JG, Craen MM.
    Prog Clin Biol Res; 1985 Jan 20; 200():113-21. PubMed ID: 2867557
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  • 16. Report on two patients with Costello syndrome and sialuria.
    Di Rocco M, Gatti R, Gandullia P, Barabino A, Picco P, Borrone C.
    Am J Med Genet; 1993 Nov 15; 47(7):1135-40. PubMed ID: 8291534
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  • 19. A mentally retarded female with distinct facial dysmorphism, joint laxity, clinodactyly and abnormal dermatoglyphics.
    Franceschini P, Guala A, Besana D, Licata D, Di Cara G, Franceschini D.
    Genet Couns; 2002 Nov 15; 13(1):55-8. PubMed ID: 12017239
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  • 20. Hypertrichosis, pigmentary retinopathy, and facial anomalies: a new syndrome?
    Pivnick EK, Wilroy RS, Martens PR, Teather TC, Hashimoto K.
    Am J Med Genet; 1996 Apr 24; 62(4):386-90. PubMed ID: 8723069
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