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Journal Abstract Search

180 related items for PubMed ID: 4725911

  • 1. The 4p-syndrome, with a report of two new cases.
    Fryns JP, Eggermont E, Verresen H, Van den Berghe H.
    Humangenetik; 1973; 19(1):99-109. PubMed ID: 4725911
    [No Abstract] [Full Text] [Related]

  • 2. 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]

  • 3. Ring-G chromosome, a new G-deletion syndrome?
    Weleber RG, Hecht F, Giblett ER.
    Am J Dis Child; 1968 Apr; 115(4):489-93. PubMed ID: 4296014
    [No Abstract] [Full Text] [Related]

  • 4. Partial deletion of the short arm of chromosome no. 4(4p-): clinical studies in five unrelated patients.
    Miller OJ, Breg WR, Warburton D, Miller DA, DeCapoa A, Allderdice PW, Davis J, Klinger HP, McGilvray E, Allen FH.
    J Pediatr; 1970 Nov; 77(5):792-801. PubMed ID: 5504070
    [No Abstract] [Full Text] [Related]

  • 5. A girl with Wolf-Hirschorn syndrome and mosaicism 46,XX-46,XX,4p-.
    Judge CG, Garson OM, Pitt DB, Sutherland GR.
    J Ment Defic Res; 1974 Mar; 18(0):79-85. PubMed ID: 4423845
    [No Abstract] [Full Text] [Related]

  • 6. [Trisomy 4p due to recombination aneusomy of an inversion 4 (p 14, q 35)].
    Rethoré MO, Dutrillaux B, Job JC, Lejeune J.
    Ann Genet; 1974 Jun; 17(2):109-14. PubMed ID: 4547937
    [No Abstract] [Full Text] [Related]

  • 7. Paternal transmission of a B-D translocation, t(4p-; 14p + or 15p+), resulting in a partial 4p trisomy.
    Gouw WL, Anders GJ, ten Kate LP, de Groot CJ.
    Humangenetik; 1972 Jun; 16(3):251-9. PubMed ID: 5082106
    [No Abstract] [Full Text] [Related]

  • 8. Prenatal recognition of 4p- syndrome.
    Blunt S, Berry AC, Seller MJ, Williams CA.
    J Med Genet; 1977 Jun; 14(3):232-3. PubMed ID: 881719
    [Abstract] [Full Text] [Related]

  • 9. The 4p- syndrome. A clinically recognizable chromosomal deletion syndrome.
    Guthrie RD, Aase JM, Asper AC, Smith DW.
    Am J Dis Child; 1971 Nov; 122(5):421-5. PubMed ID: 5129531
    [No Abstract] [Full Text] [Related]

  • 10. 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 Nov; 23(6):568-85. PubMed ID: 4134631
    [No Abstract] [Full Text] [Related]

  • 11. Microcephaly, mental retardation and hypertelorism in chromosome deletion studies.
    Miller JQ.
    Neurology; 1973 Nov; 23(11):1141-6. PubMed ID: 4795737
    [No Abstract] [Full Text] [Related]

  • 12. Human chromosomal deletion: two patients with the 4p- syndrome.
    Arias D, Passarge E, Engle MA, German J.
    J Pediatr; 1970 Jan; 76(1):82-8. PubMed ID: 5410164
    [No Abstract] [Full Text] [Related]

  • 13. [Trisomy 4p].
    Rethoré MO, Dutrillaux B, Giovannelli G, Forabosco A, Dallapiccola B, Lejeune J.
    Ann Genet; 1974 Jun; 17(2):125-8. PubMed ID: 4547940
    [No Abstract] [Full Text] [Related]

  • 14. Trisomy for the short arms of chromosome 9 in two generations, with balanced translocations t(15pplus;9qminus) in three generations.
    Podruch PE, Weisskopf B.
    J Pediatr; 1974 Jul; 85(1):92-5. PubMed ID: 4855265
    [No Abstract] [Full Text] [Related]

  • 15. Ring chromosome 10:46,XX,r(10)(p15 leads to q26).
    Tsukino R, Tsuda N, Dezawa T, Ishii T, Koike M.
    J Med Genet; 1980 Apr; 17(2):148-50. PubMed ID: 7381872
    [Abstract] [Full Text] [Related]

  • 16. Malformative syndrome with ring chromosome 13.
    Fryns JP, Deoover J, Van den Berghe H.
    Humangenetik; 1974 Apr; 24(3):235-40. PubMed ID: 4140834
    [No Abstract] [Full Text] [Related]

  • 17. Case report. Familial 4-22 translocation with partial trisomy for the short arm of chromosome 4 in two sibs.
    Sartori A, Tenconi R, Baccichetti C, Pujatti G.
    Acta Paediatr Scand; 1974 Jul; 63(4):631-5. PubMed ID: 4850900
    [No Abstract] [Full Text] [Related]

  • 18. [Familial translocation t(4;22) (p11;p12) and trisomy 4p in 2 sisters].
    Giovannelli G, Forabosco A, Dutrillaux B.
    Ann Genet; 1974 Jun; 17(2):119-24. PubMed ID: 4547939
    [No Abstract] [Full Text] [Related]

  • 19. Wolf-Hirschhorn syndrome associated with an unusual abnormality of chromosome no. 4.
    Wilson MG, Towner JW, Negus LD.
    J Med Genet; 1970 Jun; 7(2):164-70. PubMed ID: 5519605
    [No Abstract] [Full Text] [Related]

  • 20. Familial Wolf's syndrome with a hidden 4p deletion by translocation of an 8p segment. Unbalanced inheritance from a maternal translocation (4;8)(p15.3;p22). Case report, review and risk estimates.
    Stengel-Rutkowski S, Warkotsch A, Schimanek P, Stene J.
    Clin Genet; 1984 Jun; 25(6):500-21. PubMed ID: 6539659
    [Abstract] [Full Text] [Related]

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