These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

107 related items for PubMed ID: 5924747

  • 1. Trisomy No. 17-18. Report of two cases.
    Paerregaard P, Mikkelsen M, Froland A, Andersen H.
    Acta Pathol Microbiol Scand; 1966; 67(4):479-87. PubMed ID: 5924747
    [No Abstract] [Full Text] [Related]

  • 2. A newborn with multiple congenital anomalies. Trisomy 18.
    Charrow J.
    Pediatr Ann; 2007 May; 36(5):263-4. PubMed ID: 17515160
    [No Abstract] [Full Text] [Related]

  • 3. Mosaicism for trisomy 17-18 and trisomy 13-15 in man.
    Baikie AG, Garson OM, Birrell RG.
    Nature; 1965 Sep 25; 207(5004):1419-20. PubMed ID: 4957386
    [No Abstract] [Full Text] [Related]

  • 4. [Ullrich-Feichtiger's syndrome].
    Kunze J.
    Arch Kinderheilkd; 1969 Jul 25; 179(2):182-6. PubMed ID: 5802844
    [No Abstract] [Full Text] [Related]

  • 5. [Preliminary observations on 2 cases of trisomy 17-18].
    Giuffrè L, Liuzzo B.
    Minerva Pediatr; 1967 Nov 24; 19(47):2105-6. PubMed ID: 5606105
    [No Abstract] [Full Text] [Related]

  • 6. [Multiple congenital malformations in a Congolese child apparently due to trisomy 13-15].
    Ngandu-Kabeya HG, Ngwanza I, Kisula U.
    Ann Soc Belges Med Trop Parasitol Mycol; 1969 Nov 24; 49(4):341-51. PubMed ID: 4314801
    [No Abstract] [Full Text] [Related]

  • 7. [Considerations on a case of trisomy 13-15 (D 1)].
    Burdea M, Rusu I, Harmanschi A, Negrescu D, Creangă V.
    Pediatria (Bucur); 1969 Nov 24; 18(1):45-50. PubMed ID: 5780920
    [No Abstract] [Full Text] [Related]

  • 8. [THE MALFORMATIVE SYNDROME OF CHROMOSOME 18 TRISOMY].
    NIGRO N, FRANCESCHINI P, VOLANTE G.
    Minerva Pediatr; 1964 Apr 21; 16():471-80. PubMed ID: 14158345
    [No Abstract] [Full Text] [Related]

  • 9. Trisomy 18 with karyotype 47,XX,-18,+i psu dic(18p).
    Romain DR, Dagger P, Columbano-Green LM, Smythe RH, Parfitt RG.
    J Med Genet; 1992 Jul 21; 29(7):513. PubMed ID: 1640437
    [No Abstract] [Full Text] [Related]

  • 10. Trisomy 22 in a liveborn infant with multiple congenital anomalies.
    McPherson E, Stetka DG.
    Am J Med Genet; 1990 May 21; 36(1):11-4. PubMed ID: 2333899
    [Abstract] [Full Text] [Related]

  • 11. New chromosomal syndromes.
    Lewandowski RC, Yunis JJ.
    Am J Dis Child; 1975 Apr 21; 129(4):515-29. PubMed ID: 124130
    [No Abstract] [Full Text] [Related]

  • 12. Trisomy 18.
    James AE, Belcourt CL, Atkins L, Janower ML.
    Radiology; 1969 Jan 21; 92(1):37-43. PubMed ID: 4236175
    [No Abstract] [Full Text] [Related]

  • 13. Case report of a prenatal diagnosis of trisomy 13.
    Hisanaga S, Shimokawa H, Matsuo T, Nomiyama M, Nakano H.
    Nihon Sanka Fujinka Gakkai Zasshi; 1984 Mar 21; 36(3):456-8. PubMed ID: 6715930
    [No Abstract] [Full Text] [Related]

  • 14. A new translocation syndrome (3/B).
    Walzer S, Favara B, Ming PM, Gerald PS.
    N Engl J Med; 1966 Aug 11; 275(6):290-8. PubMed ID: 4957370
    [No Abstract] [Full Text] [Related]

  • 15. Familial transmission of a presumptive D/E (13-15/17-18) short arm translocation.
    Cohen MM, Lockwood MA.
    Pediatr Res; 1967 Mar 11; 1(2):104-9. PubMed ID: 6029809
    [No Abstract] [Full Text] [Related]

  • 16. Three non-mongoloid patients of similar phenotype with an extra G-like chromosome.
    Gustavson KH, Hitrec V, Santesson B.
    Clin Genet; 1972 Mar 11; 3(2):135-46. PubMed ID: 5054315
    [No Abstract] [Full Text] [Related]

  • 17.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 18. [Trisomy 18 with unusual clinical and chromosome features].
    Bruni L, Tozzi MC, Colloridi F, Lucchini R, Vitolo R, Ferri M.
    Pediatr Med Chir; 1995 Mar 11; 17(1):85-7. PubMed ID: 7739936
    [Abstract] [Full Text] [Related]

  • 19. Delayed ontogenesis in human trisomy syndromes.
    Hall B.
    Hereditas; 1965 Mar 11; 52(3):334-44. PubMed ID: 4220490
    [No Abstract] [Full Text] [Related]

  • 20. Trisomy 3 (p23-pter) resulting from maternal translocation, t (3 ; 4)(p23 ; q35).
    Schinzel A, Hanson JW, Pagon RA, Hoehn H, Smith DW.
    Ann Genet; 1978 Sep 11; 21(3):168-71. PubMed ID: 315193
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 6.