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Journal Abstract Search

124 related items for PubMed ID: 5816883

  • 1. Cornelia de Lange syndrome in an adult male.
    Cherington M, Ott JE, Robinson A.
    Neurology; 1969 Sep; 19(9):879-84. PubMed ID: 5816883
    [No Abstract] [Full Text] [Related]

  • 2. The Dyggve-Melchior-Clausen syndrome in adult siblings.
    Bonafede RP, Beighton P.
    Clin Genet; 1978 Jul; 14(1):24-30. PubMed ID: 679519
    [Abstract] [Full Text] [Related]

  • 3. Oto-palato-digital syndrome: comparison of clinical and radiographic manifestations in males and females.
    Gall JC, Stern AM, Poznanski AK, Garn SM, Weinstein ED, Hayward JR.
    Am J Hum Genet; 1972 Jan; 24(1):24-36. PubMed ID: 5012690
    [No Abstract] [Full Text] [Related]

  • 4. Skeletal changes in the Cornelia de Lange syndrome.
    Lee FA, Kenny FM.
    Am J Roentgenol Radium Ther Nucl Med; 1967 May; 100(1):27-39. PubMed ID: 6023899
    [No Abstract] [Full Text] [Related]

  • 5. Ring 1 chromosome and dwarfism--a possible syndrome.
    Wolf CB, Peterson JA, LoGrippo GA, Weiss L.
    J Pediatr; 1967 Nov; 71(5):719-22. PubMed ID: 6054759
    [No Abstract] [Full Text] [Related]

  • 6. Additional small acrocentric chromosome: two cases.
    Nielsen J, Tsuboi T, Friedrich U, Mikkelsen M, Lund B, Steinicke O.
    J Ment Defic Res; 1969 Jun; 13(2):106-22. PubMed ID: 5794285
    [No Abstract] [Full Text] [Related]

  • 7. Familial bird-headed dwarfism (Seckel's syndrome).
    Sauk JJ, Litt R, Espiritu CE, Delaney JR.
    J Med Genet; 1973 Jun; 10(2):196-8. PubMed ID: 4714590
    [Abstract] [Full Text] [Related]

  • 8. Developmental abnormalities in a patient with karyotype 46,XX,bq+.
    Chakanovskis JE, Sutherland GR.
    J Med Genet; 1970 Jun; 7(2):180-4. PubMed ID: 5519607
    [No Abstract] [Full Text] [Related]

  • 9. Cockayne's syndrome. Roentgen findings.
    Riggs W, Seibert J.
    Am J Roentgenol Radium Ther Nucl Med; 1972 Nov; 116(3):623-33. PubMed ID: 4641186
    [No Abstract] [Full Text] [Related]

  • 10. A new growth deficiency syndrome.
    Myhre SA, Ruvalcaba RH, Graham CB.
    Clin Genet; 1981 Jul; 20(1):1-5. PubMed ID: 7296942
    [No Abstract] [Full Text] [Related]

  • 11. The radiologic assessment of short stature--dwarfism.
    Dorst JP, Scott CI, Hall JG.
    Radiol Clin North Am; 1972 Aug; 10(2):393-414. PubMed ID: 4262226
    [No Abstract] [Full Text] [Related]

  • 12. An inherited small extra chromosome: a mother with 46,XX,t(17;22)(pl;ql) and a son with 47,XY,+der(22)mat.
    Borgaonkar DS, McKusick VA, Farber PA.
    J Med Genet; 1973 Dec; 10(4):379-84. PubMed ID: 4129973
    [Abstract] [Full Text] [Related]

  • 13. X-linked Dyggve-Melchior-Clausen syndrome.
    Yunis E, Fontalvo J, Quintero L.
    Clin Genet; 1980 Oct; 18(4):284-90. PubMed ID: 7192195
    [Abstract] [Full Text] [Related]

  • 14. The Cornelia de Lange syndrome in Singapore.
    Boon WH.
    J Singapore Paediatr Soc; 1969 Apr; 11(1):25-37. PubMed ID: 5366336
    [No Abstract] [Full Text] [Related]

  • 15. An (11;21) translocation in four generations with chromosome 11 abnormalities in the offspring. A clinical, cytogenetical, and gene marker study.
    Jacobsen P, Hauge M, Henningsen K, Hobolth N, Mikkelsen M, Philip J.
    Hum Hered; 1973 Apr; 23(6):568-85. PubMed ID: 4134631
    [No Abstract] [Full Text] [Related]

  • 16. An extra small metacentric chromosome in a mentally retarded boy.
    Ishmael J, Laurence KM.
    J Med Genet; 1968 Dec; 5(4):335-40. PubMed ID: 5713650
    [No Abstract] [Full Text] [Related]

  • 17. [A case of dwarfism with oto-palato-digital involvement (author's transl)].
    Farriaux JP, Dubois O, Maroteaux P, Fontaine G.
    J Radiol Electrol Med Nucl; 1974 Feb; 55(2):137-42. PubMed ID: 4408413
    [No Abstract] [Full Text] [Related]

  • 18. Bilateral split hand and split foot malformation in a boy with a de novo interstitial deletion of 7q21.3.
    Roberts SH, Hughes HE, Davies SJ, Meredith AL.
    J Med Genet; 1991 Jul; 28(7):479-81. PubMed ID: 1895319
    [Abstract] [Full Text] [Related]

  • 19. Chromosome 15 abnormality in a mentally retarded adult.
    Kelly S, Almy R, Dagle A.
    J Med Genet; 1969 Dec; 6(4):438-41. PubMed ID: 5365954
    [No Abstract] [Full Text] [Related]

  • 20. 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]

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