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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

544 related items for PubMed ID: 4469994

  • 21.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 22. Tetra-oligodactyly with bilateral aplasia and hypoplasia of long bones of upper and lower limbs: a variable manifestation of the syndrome of ectrodactyly with tibial aplasia.
    Sener RN, Sayli BS, Isikan UE, Ormeci AR, Unsal M, Tigdemir M.
    Pediatr Radiol; 1990; 21(1):57-61. PubMed ID: 2287543
    [Abstract] [Full Text] [Related]

  • 23. [Acrodolichie].
    BRUGSCH T, MOLLER H.
    Z Gesamte Inn Med; 1954 Jun 01; 9(11):521-5. PubMed ID: 13206137
    [No Abstract] [Full Text] [Related]

  • 24. Orthopaedic examination of the newborn.
    Fixsen JA.
    Nurs Mirror Midwives J; 1974 Oct 31; 139(18):57-60. PubMed ID: 4497211
    [No Abstract] [Full Text] [Related]

  • 25. Spondyloepiphyseal dysplasia congenita.
    Spranger JW, Langer LO.
    Radiology; 1970 Feb 31; 94(2):313-22. PubMed ID: 5412797
    [No Abstract] [Full Text] [Related]

  • 26. [A dominant syndrome associated with polysyndactyly, spatule thumb, facial abnormalities, and mental retardation. (A particular form of Noack's acrocephalosyndactylia)].
    Gnamey D, Farriaux JP.
    J Genet Hum; 1971 Dec 31; 19(4):299-316. PubMed ID: 5152131
    [No Abstract] [Full Text] [Related]

  • 27. A generalized disorders of the connective tissues with progeria, choanal atresia, symphalangism, hypoplasia of dentine and craniodiaphyseal hypostosis.
    Lenz WD, Majewski F.
    Birth Defects Orig Artic Ser; 1974 Dec 31; 10(12):133-6. PubMed ID: 4376705
    [No Abstract] [Full Text] [Related]

  • 28. Spondylometaphyseal dysplasia: a variant form.
    Felman AH, Frias JL, Rennert OM.
    Radiology; 1974 Nov 31; 113(2):409-15. PubMed ID: 4419008
    [No Abstract] [Full Text] [Related]

  • 29. Radiological findings in the DOOR syndrome.
    Thomas PS, Nevin NC.
    Ann Radiol (Paris); 1982 Jan 31; 25(1):54-8. PubMed ID: 7065610
    [No Abstract] [Full Text] [Related]

  • 30. Hereditary brachydactyly.
    Hoefnagel D, Gerald PS.
    Ann Hum Genet; 1966 May 31; 29(4):377-82. PubMed ID: 5961825
    [No Abstract] [Full Text] [Related]

  • 31. The REEDS syndrome.
    Reed WB, Brown AC, Sugarman GI, Schlesinger L.
    Birth Defects Orig Artic Ser; 1974 May 31; 10(5):61-73. PubMed ID: 4220009
    [No Abstract] [Full Text] [Related]

  • 32. [Association of deformities of the head and extremities. Apropos of 15 cases].
    Brunais B, Flageul G, Grignon JL.
    Rev Stomatol Chir Maxillofac; 1982 May 31; 83(1):36-8. PubMed ID: 6950486
    [No Abstract] [Full Text] [Related]

  • 33. [Localized and correlated skeletal abnormalities. A selection].
    Swoboda W.
    Fortschr Geb Rontgenstrahlen Nuklearmed Erganzungsbd; 1969 May 31; 78():98-120. PubMed ID: 4393890
    [No Abstract] [Full Text] [Related]

  • 34. Otopalatodigital syndrome: radiologic findings in the hand and foot.
    Poznanski AK, Macpherson RI, Dijkman DJ, Gorlin RJ, Gall JC, Stern AM, Garn SM, Nagy JM.
    Birth Defects Orig Artic Ser; 1974 May 31; 10(5):125-39. PubMed ID: 4469976
    [No Abstract] [Full Text] [Related]

  • 35. [Reductional anomalies of the limbs].
    Walbaum R.
    LARC Med; 1982 Dec 31; 2(11):968-77. PubMed ID: 6761523
    [No Abstract] [Full Text] [Related]

  • 36. Brachydactyly type E in two sibs with increased bone density and mental retardation. A new autosomal recessive syndrome?
    Stoll C, Alembik Y.
    Genet Couns; 2004 Dec 31; 15(4):421-8. PubMed ID: 15658617
    [Abstract] [Full Text] [Related]

  • 37. Brachydactyly with absence of middle phalanges and hypoplastic nails. A new hereditary syndrome.
    Cuevas-Sosa A, García-Segur F.
    J Bone Joint Surg Br; 1971 Feb 31; 53(1):101-5. PubMed ID: 4325377
    [No Abstract] [Full Text] [Related]

  • 38. Fused eyelids, airway anomalies, ovarian cysts, and digital abnormalities in siblings: a new autosomal recessive syndrome or a variant of Fraser syndrome?
    Mena W, Krassikoff N, Philips JB.
    Am J Med Genet; 1991 Sep 01; 40(3):377-82. PubMed ID: 1951446
    [Abstract] [Full Text] [Related]

  • 39. A distinct autosomal dominant craniosynostosis-brachydactyly syndrome.
    Glass IA, Chapman S, Hockley AD.
    Clin Dysmorphol; 1994 Jul 01; 3(3):215-23. PubMed ID: 7981856
    [Abstract] [Full Text] [Related]

  • 40. Brachydactyly and polydactyly with dermal ridge dissociation and ridge hypoplasia.
    Crawfurd MD, Saldaña-Garcia P.
    J Med Genet; 1979 Oct 01; 16(5):402-5. PubMed ID: 513089
    [Abstract] [Full Text] [Related]

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