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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

115 related articles for article (PubMed ID: 4117155)

  • 1. Monosomy 21 in spontaneous abortus.
    Ohama K; Kajii T
    Humangenetik; 1972; 16(3):267-70. PubMed ID: 4117155
    [No Abstract]   [Full Text] [Related]  

  • 2. Trisomy 14 in spontaneous abortus.
    Kajii T; Oama K; Ferrier A
    Humangenetik; 1972; 15(3):265-7. PubMed ID: 4117151
    [No Abstract]   [Full Text] [Related]  

  • 3. Monosomy of chromosome No. 22. A case report.
    DeCicco F; Steele MW; Pan S; Park SC
    J Pediatr; 1973 Nov; 83(5):836-8. PubMed ID: 4126387
    [No Abstract]   [Full Text] [Related]  

  • 4. Monosomy of a G chromosome in spontaneous abortions.
    Larson SL; Aaro LA; Titus JL
    Am J Obstet Gynecol; 1970 Feb; 106(4):622-3. PubMed ID: 5412858
    [No Abstract]   [Full Text] [Related]  

  • 5. [Role of BoBs technology in early missed abortion chorionic villi].
    Li ZY; Liu XY; Peng P; Chen N; Ou J; Hao N; Zhou J; Bian XM
    Zhonghua Fu Chan Ke Za Zhi; 2018 May; 53(5):308-312. PubMed ID: 29804348
    [No Abstract]   [Full Text] [Related]  

  • 6. Double heteroploidy, 46, XY, t(13q14q), +18, in a spontaneous abortus.
    Avirachan S; Kajii T
    Clin Genet; 1973; 4(2):101-4. PubMed ID: 4730938
    [No Abstract]   [Full Text] [Related]  

  • 7. Monosomy for the centromeric and juxtacentromeric region of chromosome 21.
    Holbek S; Friedrich U; Brostrom K; Petersen GB
    Humangenetik; 1974; 24(3):191-5. PubMed ID: 4140831
    [No Abstract]   [Full Text] [Related]  

  • 8. Monosomy 21 in a human spontaneous abortus. Morphogenetic disturbances and phenotype at the cellular level.
    Kuliev AM; Grinberg KN; Kukharenko VI; Kulazenko VP; Bogomazov EA
    Hum Genet; 1977 Sep; 38(2):137-45. PubMed ID: 908560
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Monosomy 22 with humoral immunodeficiency: is there an immunoglobulin chain deficit?
    García Miranda JL; Otero Gómez A; Varela Ansedes H; Rancel Torres N; González Espinosa C; Cortabarría C; Sánchez Salgado G
    J Med Genet; 1983 Feb; 20(1):69-72. PubMed ID: 6842539
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Do chromosomal abnormalities reappear in subsequent pregnancies and how often?].
    Skrzypczak J; Kwinecka-Dmitriew B; Zakrzewska M; Latos-Bieleńska A
    Ginekol Pol; 2010 Sep; 81(9):681-6. PubMed ID: 20973205
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Aneuploidy screening in a coelomic sample from a missed abortion using sequential fluorescence in situ hybridization.
    Chatzimeletiou K; Makrydimas G; Nicolaides KH
    Fertil Steril; 2006 Apr; 85(4):1059.e13-6. PubMed ID: 16580397
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Familial translocation 15-22. A possible cause for abortions in female carriers.
    Fried K; Bukovsky J; Rosenblatt M; Mundel G
    J Med Genet; 1974 Sep; 11(3):280-2. PubMed ID: 4431033
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Amnion rupture sequence in a first trimester missed abortion.
    Philipp T; Kalousek DK
    Prenat Diagn; 2001 Oct; 21(10):835-8. PubMed ID: 11746124
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [A case with mosaicism of partial monosomy G- monosomy G in peripheral blood lymphocytes].
    Bauchinger M; Schmid E; Röttinger E
    Humangenetik; 1968; 6(4):303-10. PubMed ID: 5713616
    [No Abstract]   [Full Text] [Related]  

  • 15. [Chromosome aberrations in abortions].
    Boué JG; Boué A; Lazar P
    Ann Genet; 1967 Dec; 10(4):179-87. PubMed ID: 5301690
    [No Abstract]   [Full Text] [Related]  

  • 16. Trypsin banding of Giemsa-stained chromosomes.
    Kajii T; Oama K; Avirachan S; Avirachan TT
    Lancet; 1972 Dec; 2(7790):1311-2. PubMed ID: 4117839
    [No Abstract]   [Full Text] [Related]  

  • 17. Familial cases of marker chromosomes of groups 21-22 and 13-15 (Gpss and Dp+).
    Kyaosaar ME
    Sov Genet; 1973 Nov; 7(7):913-8. PubMed ID: 4777944
    [No Abstract]   [Full Text] [Related]  

  • 18. [Viability in monosomy G].
    Böhm R; Fuhrmann W
    Monatsschr Kinderheilkd (1902); 1969 Apr; 117(4):184-7. PubMed ID: 5377498
    [No Abstract]   [Full Text] [Related]  

  • 19. [Monosomy for the centromeric regions of chromosome 21].
    Rethoré MO; Dutrillaux B; Baheux G; Gerveaux J; Lejeune J
    Exp Cell Res; 1972 Feb; 70(2):455-6. PubMed ID: 5058917
    [No Abstract]   [Full Text] [Related]  

  • 20. An association between sex chromosomal aneuploidy in sperm and an abortus with 45,X of paternal origin: possible transmission of chromosomal abnormalities through ICSI.
    Tang SS; Gao H; Robinson WP; Ho Yuen B; Ma S
    Hum Reprod; 2004 Jan; 19(1):147-51. PubMed ID: 14688173
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.