BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

103 related articles for article (PubMed ID: 3746843)

  • 21. Chromosome abnormalities associated with recurrent abortion.
    Imai A; Tamaya T
    Res Commun Mol Pathol Pharmacol; 1996 Dec; 94(3):323-6. PubMed ID: 9029678
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Unusual chromosome 9 polymorphism and reproductive failure.
    Fryns JP; Kleczkowska A; Londers L; van den Berghe H
    Ann Genet; 1985; 28(1):49-51. PubMed ID: 3874589
    [TBL] [Abstract][Full Text] [Related]  

  • 23. [Structural chromosomal rearrangements in couples with repeated miscarriages. Experience in Louvain].
    Fryns JP; Kleczkowska A; Kubien E; van den Berghe H
    J Genet Hum; 1988 Jan; 36(1-2):59-61. PubMed ID: 3379379
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Cytogenetic aspects of habitual abortion. 2. Observation of satellite association in couples with history of habitual abortion.
    Koike K
    Nagoya Med J; 1970 Nov; 16(2):72-9. PubMed ID: 5496710
    [No Abstract]   [Full Text] [Related]  

  • 25. [A rare case of a chromosome 15:15 translocation carrier causing habitual abortion].
    Hu HY
    Zhonghua Fu Chan Ke Za Zhi; 1982 Oct; 17(4):193-5. PubMed ID: 7151529
    [No Abstract]   [Full Text] [Related]  

  • 26. Chromosome aberrations in the parents in the case of repeated spontaneous abortions.
    Kulazhenko VP; Lazyuk GI; Levchenko NN; Savenko LA; Usoev SS; Kotovich LG; Zhukova TV; Podleshchuk LV
    Sov Genet; 1974 Jul; 8(7):921-8. PubMed ID: 4422175
    [No Abstract]   [Full Text] [Related]  

  • 27. Cytogenetics of habitual abortion.
    Stenchever MA; Jarvis JA; Macintyre MN
    Obstet Gynecol; 1968 Oct; 32(4):548-55. PubMed ID: 5742467
    [No Abstract]   [Full Text] [Related]  

  • 28. Cytogenetics of habitual abortion. A review.
    Khudr G
    Obstet Gynecol Surv; 1974 May; 29(5):290-310. PubMed ID: 4615284
    [No Abstract]   [Full Text] [Related]  

  • 29. Cytogenetics of recurrent abortion or unsuccessful pregnancy.
    De la Chapelle A; Schröder J; Kokkonen J
    Int J Fertil; 1973; 18(4):215-9. PubMed ID: 4130032
    [No Abstract]   [Full Text] [Related]  

  • 30. [Correlation of the clinical phenotype with a pericentric inversion of chromosome 9].
    Scarinci R; Anichini C; Vivarelli R; Berardi R; Pucci L; Rosaia L; Tomaccini D
    Boll Soc Ital Biol Sper; 1992 Mar; 68(3):175-81. PubMed ID: 1389073
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Inheritance of pericentric inversion in chromosome 7 through the three progenies and a newborn with congenital hydronephrosis diagnosed prenatally by fetal urine sampling.
    Demirhan O; Ozcan K; Taştemir D; Demir C; Tunç E; Solğun HA; Güzel AI
    Fertil Steril; 2008 Jan; 89(1):228.e1-6. PubMed ID: 17880960
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Mitotic disturbances associated with inversion 9qh. A case report.
    Murthy SK; Prabhakara K
    Ann Genet; 1990; 33(3):169-72. PubMed ID: 2149631
    [TBL] [Abstract][Full Text] [Related]  

  • 33. [Analysis of chromosome karyotypes in 210 couples with repeated spontaneous abortions].
    Fan XG
    Zhonghua Fu Chan Ke Za Zhi; 1986 Sep; 21(5):287-90, 318. PubMed ID: 3816399
    [No Abstract]   [Full Text] [Related]  

  • 34. [Mother with D/D translocation in genetic counseling].
    Stepien J; Raczkiewicz B
    Ginekol Pol; 1977 Mar; 48(3):285-8. PubMed ID: 558134
    [No Abstract]   [Full Text] [Related]  

  • 35. A prospective, cytogenetic study of recurrent abortion.
    Wilson JA
    J Med Genet; 1969 Mar; 6(1):5-13. PubMed ID: 5771225
    [No Abstract]   [Full Text] [Related]  

  • 36. [Example of the significance of cytogenetic examinations in habitual abortions].
    Knörr K; Knörr-Gärtner H; Uebele-Kallhardt B
    Geburtshilfe Frauenheilkd; 1969 Sep; 29(9):792-800. PubMed ID: 5344459
    [No Abstract]   [Full Text] [Related]  

  • 37. Familial paracentric inversion of chromosome 15 (q15q24).
    Del Porto G; D'Alessandro E; De Matteis C; D'Innocenzo R; Baldi M; Pachi A; Cappa F
    J Med Genet; 1984 Dec; 21(6):451-3. PubMed ID: 6512834
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Paternal pericentric inversion of chromosome 4 as a cause of recurrent pregnancy loss.
    Wolf GC; Mao J; Izquierdo L; Joffe G
    J Med Genet; 1994 Feb; 31(2):153-5. PubMed ID: 8182725
    [TBL] [Abstract][Full Text] [Related]  

  • 39. [The role of chromosomes in the aetiology of human abortion].
    Kotzé GM; Retief AE
    S Afr Med J; 1978 Sep; 54(14):562-6. PubMed ID: 734601
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Familial dicentric translocation t(13;18)(p13;p11.2) ascertained by recurrent miscarriages.
    Daniel A; Perel ID; Clarke AJ; Saville T
    J Med Genet; 1979 Feb; 16(1):73-5. PubMed ID: 469891
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 6.