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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

185 related items for PubMed ID: 6212507

  • 41. Reconstructive surgery of major congenital skeletal deformities of the limbs.
    Sharrard WJ.
    Dev Med Child Neurol; 1969 Apr; 11(2):153-61. PubMed ID: 5787714
    [No Abstract] [Full Text] [Related]

  • 42. Metaphyseal dysostosis, conductive hearing loss and mental retardation: a recessively inherited syndrome.
    Rimoin DL, McAlister WH.
    Birth Defects Orig Artic Ser; 1971 Mar; 07(4):116-22. PubMed ID: 5173335
    [Abstract] [Full Text] [Related]

  • 43. Dwarfism with congenital bowing of long bones.
    Folman Y, Liberty S.
    Isr J Med Sci; 1989 Jan; 25(1):49-51. PubMed ID: 2925362
    [No Abstract] [Full Text] [Related]

  • 44. Dyschondrosteosis. A Mexican family with two affected males.
    Lisker R, Gamboa I, Hernández J.
    Clin Genet; 1972 Jan; 3(3):154-7. PubMed ID: 5054807
    [No Abstract] [Full Text] [Related]

  • 45. [The Leri-Weill syndrome. Illustration of a case].
    Chiappo GF, Mignone F, Zannino L.
    Minerva Pediatr; 1973 Sep 15; 25(31):1315-26. PubMed ID: 4766776
    [No Abstract] [Full Text] [Related]

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  • 49. Anauxetic dysplasia: A rare clinical entity.
    Akgün-Doğan Ö, Şimsek-Kiper PÖ, Utine GE, Boduroğlu K.
    Turk J Pediatr; 2018 Sep 15; 60(1):89-93. PubMed ID: 30102486
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  • 51. Dyschondrosteose. Mesomelic dwarfism of Lwei and Weill.
    Felman AH, Kirkpatrick JA.
    Am J Dis Child; 1970 Oct 15; 120(4):329-31. PubMed ID: 5493830
    [No Abstract] [Full Text] [Related]

  • 52. Mesomelic dysplasia with absence of fibulae and hexadactyly: Nievergelt syndrome or new syndrome?
    Petrella R, Ludman MD, Rabinowitz JG, Gilbert F, Hirschhorn K.
    Am J Med Genet; 1990 Sep 15; 37(1):10-4. PubMed ID: 2240023
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  • 59. [A case of metatropic dwarfism (author's transl)].
    Pinto R, De Bellis U, Cicale F.
    Radiol Med; 1976 Jan 15; 62(1):49-55. PubMed ID: 1005788
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  • 60. A distinct lethal neonatal chondrodysplasia with snail-like pelvis: Schneckenbecken dysplasia.
    Borochowitz Z, Jones KL, Silbey R, Adomian G, Lachman R, Rimoin DL.
    Am J Med Genet; 1986 Sep 15; 25(1):47-59. PubMed ID: 3799723
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