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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]
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]
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]