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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

288 related items for PubMed ID: 4402497

  • 21.
    ; . PubMed ID:
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  • 23. Smith-Lemli-Opitz syndrome: review and report of two affected siblings.
    Johnson VP.
    Z Kinderheilkd; 1975; 119(4):221-34. PubMed ID: 166525
    [Abstract] [Full Text] [Related]

  • 24. Silver-Russell syndrome with absence of digits and syndactylism of the fingers.
    Keppen LD, Rennert OM.
    Clin Genet; 1983 Dec; 24(6):453-5. PubMed ID: 6317237
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  • 25.
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  • 26. Skeletal anomalies in genetically determined congenital heart disease.
    Poznanski AK, Stern AM, Gall JC.
    Radiol Clin North Am; 1971 Dec; 9(3):435-58. PubMed ID: 5145748
    [No Abstract] [Full Text] [Related]

  • 27. Proteus syndrome.
    Samlaska CP, Levin SW, James WD, Benson PM, Walker JC, Perlik PC.
    Arch Dermatol; 1989 Aug; 125(8):1109-14. PubMed ID: 2667470
    [Abstract] [Full Text] [Related]

  • 28. The trisomy 8 syndrome: report of two further cases.
    Jacobsen P, Mikkelsen M, Rosleff F.
    Ann Genet; 1974 Jun; 17(2):87-94. PubMed ID: 4547945
    [No Abstract] [Full Text] [Related]

  • 29. Distal obstructive uropathy with polydactyly: a new syndrome?
    Halal F.
    Am J Med Genet; 1986 Aug; 24(4):753-7. PubMed ID: 3740105
    [No Abstract] [Full Text] [Related]

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

  • 31.
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  • 33. [High-grade numerical plus variant of the hand and foot].
    Schenk R, Jacquemain B.
    Z Orthop Ihre Grenzgeb; 1969 Jan; 105(4):515-27. PubMed ID: 4240747
    [No Abstract] [Full Text] [Related]

  • 34. 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; 53(1):101-5. PubMed ID: 4325377
    [No Abstract] [Full Text] [Related]

  • 35.
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  • 36. Yunis-Varon syndrome.
    Bhatia S, Holla RG.
    Indian Pediatr; 2005 Apr; 42(4):373-5. PubMed ID: 15876600
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  • 37. Acral dysostosis dyserythropoiesis syndrome.
    Le Merrer M, Girot R, Parent P, Cormier-Daire V, Maroteaux P.
    Eur J Pediatr; 1995 May; 154(5):384-8. PubMed ID: 7641772
    [Abstract] [Full Text] [Related]

  • 38. Autosomal recessive postaxial polydactyly: report of a family.
    Cantú JM, del Castillo V, Cortes R, Urrusti J.
    Birth Defects Orig Artic Ser; 1974 May; 10(5):19-22. PubMed ID: 4469981
    [No Abstract] [Full Text] [Related]

  • 39. Further delineation of the KBG syndrome.
    Devriendt K, Holvoet M, Fryns JP.
    Genet Couns; 1998 May; 9(3):191-4. PubMed ID: 9777340
    [Abstract] [Full Text] [Related]

  • 40. The otopalatodigital (OPD) syndrome: (conductive deafness, cleft palate and anomaly of digits).
    Nager GT, Char F.
    Birth Defects Orig Artic Ser; 1971 Jun; 7(7):273-4. PubMed ID: 5173224
    [No Abstract] [Full Text] [Related]

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