152 related articles for article (PubMed ID: 3879450)
1. Genetic factors influencing aneuploidy frequency.
Warburton D
Basic Life Sci; 1985; 36():133-48. PubMed ID: 3879450
[No Abstract] [Full Text] [Related]
2. Banding analysis of abnormal karyotypes in spontaneous abortion.
Kajii T; Oama K; Niikawa N; Ferrier A; Avirachan S
Am J Hum Genet; 1973 Sep; 25(5):539-47. PubMed ID: 4741848
[No Abstract] [Full Text] [Related]
3. Antenatal diagnosis of chromosomal disorders.
Simpson JL
Clin Obstet Gynaecol; 1980 Apr; 7(1):13-26. PubMed ID: 6445807
[No Abstract] [Full Text] [Related]
4. The origin of aneuploidy in humans.
Hassold TJ
Basic Life Sci; 1985; 36():103-15. PubMed ID: 3006652
[No Abstract] [Full Text] [Related]
5. Parental origin of chromosome abnormalities in spontaneous abortions.
Meulenbroek GH; Geraedts JP
Hum Genet; 1982; 62(2):129-33. PubMed ID: 7160845
[TBL] [Abstract][Full Text] [Related]
6. [Cytogenetic examination in gynecology and obstetrics].
Knörr K
Med Klin; 1974 Jan; 69(3):75-82. PubMed ID: 4274010
[No Abstract] [Full Text] [Related]
7. Chromosomes and abortion.
Carr DH
Adv Hum Genet; 1971; 2():201-57. PubMed ID: 4950477
[No Abstract] [Full Text] [Related]
8. [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]
9. Chromosome abnormalities and abortion.
Boué A; Boué J
Basic Life Sci; 1974; 4(PT. B):317-39. PubMed ID: 4618118
[No Abstract] [Full Text] [Related]
10. [Prenatal chromosome analysis using the FISH technique allows fetal aneuploidy detection within a few hours].
Steinborn A; Röddiger S; Born HJ; Baier P; Halberstadt E
Z Geburtshilfe Neonatol; 1996; 200(5):186-90. PubMed ID: 9035828
[TBL] [Abstract][Full Text] [Related]
11. [Familial translocation t(6; 18) (q16; q16; q23) with free 21 trisomy].
Tenconi R; Baccichetti C; Dussini N; Panizza G
Ann Genet; 1974 Dec; 17(4):275-7. PubMed ID: 4281288
[No Abstract] [Full Text] [Related]
12. 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]
13. Chromosomal differences in susceptibility to meiotic aneuploidy.
Warburton D; Kinney A
Environ Mol Mutagen; 1996; 28(3):237-47. PubMed ID: 8908182
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. Proximal 14 trisomy 46,XX, -22 +der(14)t(14;22) (q21;q11)mat.
Fried K; Goldberg MD; Rosenblatt M
Teratology; 1980 Jun; 21(3):309-12. PubMed ID: 7455919
[No Abstract] [Full Text] [Related]
16. Maternal age-specific rates of numerical chromosome abnormalities with special reference to trisomy.
Hassold T; Chiu D
Hum Genet; 1985; 70(1):11-7. PubMed ID: 3997148
[TBL] [Abstract][Full Text] [Related]
17. Homozygosity for a Y/22 chromosome translocation: t(Y;22) (q12;p12/13).
Leschot NJ; von den Velden J; Marinkovic-Ilsen A; Darling SM; Nijenhuis LE
Clin Genet; 1986 Mar; 29(3):251-7. PubMed ID: 3698333
[TBL] [Abstract][Full Text] [Related]
18. [Morphological study of human embryos with chromosome aberrations].
Roux C
Presse Med (1893); 1970 Mar; 78(14):647-52. PubMed ID: 5462256
[No Abstract] [Full Text] [Related]
19. An inherited translocation t(4;15) (p16;q22) leading to two cases of partial trisomy 15.
Cohen MM; Ornoy A; Rosenmann A; Kohn G
Ann Genet; 1975 Jun; 18(2):99-103. PubMed ID: 1081372
[TBL] [Abstract][Full Text] [Related]
20. [Segregation problems in balanced structural chromosome rearrangements].
Dagna Bricarelli F; Doria Lamba Carbone L; Frateschi M
Pathologica; 1983; 75 Suppl():81-95. PubMed ID: 6393020
[No Abstract] [Full Text] [Related]
[Next] [New Search]
