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6. Translocation between both members of chromosome pair number 15 causing recurrent abortions. Lucas M Ann Hum Genet; 1969 May; 32(4):347-52. PubMed ID: 5822322 [No Abstract] [Full Text] [Related]
7. A possible case of partial trisomy for chromosome 22: further evidence from Giemsa banding studies. Sands ME J Ment Defic Res; 1974 Dec; 18(4):327-30. PubMed ID: 4142949 [No Abstract] [Full Text] [Related]
8. Inherited (13;14) translocation and reproduction. Report on three families. von Koskull H; Aula P Humangenetik; 1974; 24(2):85-91. PubMed ID: 4139103 [No Abstract] [Full Text] [Related]
9. Successive spontaneous abortions with diverse chromosomal aberrations in human translocation heterozygote. Kohn G; Ornoy A; Ben-Tsur Z; Sadovsky E; Cohen MM Teratology; 1975 Dec; 12(3):283-9. PubMed ID: 1198335 [TBL] [Abstract][Full Text] [Related]
10. Parental chromosomal aberrations associated with multiple abortions and an abnormal infant. Hsu LY; Barcinski M; Shapiro LR; Valderrama E; Gertner M; Hirschhorn K Obstet Gynecol; 1970 Nov; 36(5):723-30. PubMed ID: 5474003 [No Abstract] [Full Text] [Related]
11. 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]
12. Trisomy-16 in a mosaic carrier father and his aborted foetus. Arakaki DT; Waxman SH J Med Genet; 1969 Mar; 6(1):85-8. PubMed ID: 5814232 [No Abstract] [Full Text] [Related]
13. Craniorachischisis in a partially trisomic 11 fetus in a family with reproductive failure and a reciprocal translocation, t(6p plus;11q minus). Wright YM; Clark WE; Breg WR J Med Genet; 1974 Mar; 11(1):69-75. PubMed ID: 4134620 [TBL] [Abstract][Full Text] [Related]
14. Cytogenetics of habitual abortion and other reproductive wastage. Stenchever MA; Parks KJ; Daines TL; Allen MA; Stenchever MR Am J Obstet Gynecol; 1977 Jan; 127(2):143-50. PubMed ID: 556663 [No Abstract] [Full Text] [Related]
15. Multicolour spectral karyotyping for complex chromosomal rearrangements in repeated abortion or congenital anomalies. Tanemura M; Suzumori K; Nishikawa N; Ishihara Y Prenat Diagn; 2001 Dec; 21(13):1123-8. PubMed ID: 11787036 [TBL] [Abstract][Full Text] [Related]
16. Cytogenetic findings in 122 couples with recurrent abortions. Stoll C Hum Genet; 1981; 57(1):101-3. PubMed ID: 7262863 [TBL] [Abstract][Full Text] [Related]
17. [Autoradiographic studies of human chromosomes. VII. 5 cases of familial t(DqDq)]. de Grouchy J; Crippa L; German J Ann Genet; 1970 Mar; 13(1):19-37. PubMed ID: 5310103 [No Abstract] [Full Text] [Related]
18. [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]
19. Familial C/D translocation t(9;13)(9p23.13q21) in a male associated with recurrent abortion. Singh-Kahlon D; Serra A Hum Genet; 1976 Aug; 33(3):223-30. PubMed ID: 964984 [TBL] [Abstract][Full Text] [Related]
20. [Chromosome analysis in abortion]. Rosenkranz W; Zierler H Wien Med Wochenschr; 1990; 140(22):545-7. PubMed ID: 2080627 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]