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

166 related items for PubMed ID: 6723106

  • 21. [Trisomy of the distal 15q region due to familial balanced translocation t(15;16)(q24;p13) and unusual mosaicism in the mother of the proband].
    Nazarenko SA, Nazarenko LP, Baranova VA.
    Tsitol Genet; 1987; 21(6):434-7. PubMed ID: 3445362
    [Abstract] [Full Text] [Related]

  • 22. Trisomy 6q22 leads to 6qter due to maternal 6;21 translocation. Case report review of the literature.
    Taysi K, Chao WT, Monaghan N, Monaco MP.
    Ann Genet; 1983; 26(4):243-6. PubMed ID: 6364954
    [Abstract] [Full Text] [Related]

  • 23. Five generations of t(4;8)(q35;q13) leading to a case of partial 8q trisomy with consideration of potential pregnancy outcomes from translocation carriers.
    Young RS, Hansen KL, Khodr GS.
    Clin Genet; 1984 Jun; 25(6):522-7. PubMed ID: 6733948
    [Abstract] [Full Text] [Related]

  • 24.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 25.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 26.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 27. Cri du chat-syndrome in combination with partial trisomy 9 p.
    Sigmund J, Frisch H, Heinz-Erian P, Rhomberg K, Wegner RD.
    Padiatr Padol; 1986 Jun; 21(1):61-7. PubMed ID: 3960564
    [Abstract] [Full Text] [Related]

  • 28. [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 Jun; 18(3):223-8. PubMed ID: 6235655
    [Abstract] [Full Text] [Related]

  • 29. Trisomy 18q: 46,XX,13q+,t(13;18)(q32;q11) in a newborn associated with multiple congenital anomalies due to paternal reciprocal translocation, 46,XY,-13,+der(13),t(13;18)(q32;q11).
    Murthy DS, Patel ZM, Ambani LM.
    Clin Genet; 1980 Oct; 18(4):233-8. PubMed ID: 7438504
    [Abstract] [Full Text] [Related]

  • 30.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 31. 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 Oct; 11(4):355-61. PubMed ID: 11140413
    [Abstract] [Full Text] [Related]

  • 32.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 33.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 34.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 35.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 36. Partial monosomy and partial trisomy for different segments of chromosome 13 in several individuals of the same family.
    Wilroy RS, Summitt RL, Martens P, Gooch WM, Hood C, Wiser W.
    Birth Defects Orig Artic Ser; 1976 Oct; 12(5):161-7. PubMed ID: 953218
    [No Abstract] [Full Text] [Related]

  • 37.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 38.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 39. Partial and complete trisomy 9: delineation of a trisomy 9 syndrome.
    Sutherland GR, Carter RF, Morris LL.
    Hum Genet; 1976 May 19; 32(2):133-40. PubMed ID: 1270071
    [Abstract] [Full Text] [Related]

  • 40. Partial 18 trisomy (with 47 chromosomes) resulting from a familial maternal translocation.
    Fried K, Bar-Yochai A, Rosenblatt M, Mundel G.
    J Med Genet; 1978 Feb 19; 15(1):76-8. PubMed ID: 633321
    [Abstract] [Full Text] [Related]

    Page: [Previous] [Next] [New Search]
    of 9.