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

154 related items for PubMed ID: 4430152

  • 1. 47, XY, t(9pplus;11qplus) in a mlae infant with multiple malformations.
    Dinno ND, Silvey GL, Weisskopf B.
    Clin Genet; 1974; 6(2):125-31. PubMed ID: 4430152
    [No Abstract] [Full Text] [Related]

  • 2.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 3. [Trisomy 10p as a result of familial 10/22 translocation].
    Zergollern L, Begovic D, Muzinić D.
    Acta Med Iugosl; 1980; 34(2):113-22. PubMed ID: 7405617
    [No Abstract] [Full Text] [Related]

  • 4.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 5. [Contribution and considerations on cranio-facial abnormalities caused by chromosomic aberrations in children].
    Infortuna M, Gattarello A, Corrado F.
    Pediatr Med Chir; 1984; 6(3):415-23. PubMed ID: 6533589
    [Abstract] [Full Text] [Related]

  • 6.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 7.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 8.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 9.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 10. [Partial C trisomy through translocation t(Cp-;Gp-)].
    Deminatti M, Maillard E, Gosselin B, Peltier JM, Bulteel MF, Dupuis C.
    Ann Genet; 1969 Mar; 12(1):36-45. PubMed ID: 5306710
    [No Abstract] [Full Text] [Related]

  • 11. An unusual clinical characterization of a male with distal partial trisomy 1q42.1 and monosomy 4q35.1 and review of the literature.
    Wang CB, Lin SP, Chen CP, Chen YJ, Lee CC.
    Genet Couns; 2006 Mar; 17(4):435-40. PubMed ID: 17375530
    [Abstract] [Full Text] [Related]

  • 12.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 13.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 14. Two cases of partial trisomy 10q syndrome due to a familial 10;20 translocation.
    Tüysüz B, Hacihanefioglu S, Silahtaroglu A, Yilmaz S, Deviren A, Cenani A.
    Genet Couns; 2000 Mar; 11(4):355-61. PubMed ID: 11140413
    [Abstract] [Full Text] [Related]

  • 15. [Partial trisomy (10pter leads to 10q21) and partial monosomy (21pter leads to 21q21) due to a reciprocal balanced familial translocation (10;21)(q21;q21) (author's transl)].
    Obry E, Piussan C, Risbourg B, Dutrillaux B.
    Ann Genet; 1980 Mar; 23(4):216-20. PubMed ID: 6971599
    [Abstract] [Full Text] [Related]

  • 16.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 17. Trisomy 9p resulting from maternal 9/21 translocation.
    Sŭbrt I, Blehová B, Pallová B.
    Hum Genet; 1976 May 19; 32(2):217-20. PubMed ID: 944684
    [Abstract] [Full Text] [Related]

  • 18.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 19. [Multiple chromosome aberrations in 3 generations of a family and Down's syndrome resulting from partial trisomy of chromosome 21 (q21--q22)].
    Butomo IV, Prozorova MV, Khitrikova LE.
    Tsitol Genet; 1984 May 19; 18(3):223-8. PubMed ID: 6235655
    [Abstract] [Full Text] [Related]

  • 20. Trisomy 10p, due to an unusual translocation.
    Orye E, Van Haesebrouck P, Van Coster R, Van Mele B.
    J Genet Hum; 1985 Jan 19; 33(1):63-6. PubMed ID: 3981144
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 8.