184 related articles for article (PubMed ID: 6478636)
1. Fragile sites and chromosome breakpoints in constitutional rearrangements I. Amniocentesis.
Hecht F; Hecht BK
Clin Genet; 1984 Sep; 26(3):169-73. PubMed ID: 6478636
[TBL] [Abstract][Full Text] [Related]
2. Fragile sites and chromosome breakpoints in constitutional rearrangements II. Spontaneous abortions, stillbirths and newborns.
Hecht F; Hecht BK
Clin Genet; 1984 Sep; 26(3):174-7. PubMed ID: 6478637
[TBL] [Abstract][Full Text] [Related]
3. No statistical association between fragile sites and constitutional chromosome breakpoints.
Mariani T; Musio A; Simi S
Cancer Genet Cytogenet; 1995 Nov; 85(1):78-81. PubMed ID: 8536244
[TBL] [Abstract][Full Text] [Related]
4. Fragile sites and breakpoints in constitutional rearrangements and in human sperm chromosomes.
Fuster C; MirĂ³ R; Templado C; Barrios L; Moreno V; Egozcue J
Hum Genet; 1989 Jul; 82(4):330-4. PubMed ID: 2737665
[TBL] [Abstract][Full Text] [Related]
5. Breakpoint distribution in constitutional chromosome rearrangements with respect to fragile sites.
Porfirio B; Dallapiccola B; Terrenato L
Ann Hum Genet; 1987 Oct; 51(4):329-36. PubMed ID: 3447515
[TBL] [Abstract][Full Text] [Related]
6. Fragile sites, cancer chromosome breakpoints, and oncogenes all cluster in light G bands.
Hecht F
Cancer Genet Cytogenet; 1988 Mar; 31(1):17-24. PubMed ID: 3162186
[TBL] [Abstract][Full Text] [Related]
7. Cancer chromosome breakpoints and common fragile sites induced by aphidicolin.
Hecht F; Glover TW
Cancer Genet Cytogenet; 1984 Oct; 13(2):185-8. PubMed ID: 6434179
[TBL] [Abstract][Full Text] [Related]
8. Fragile sites and chromosome breakpoints in constitutional rearrangements.
De Braekeleer M
Clin Genet; 1985 May; 27(5):523-4. PubMed ID: 4006280
[No Abstract] [Full Text] [Related]
9. Chromosomal breakpoints in aborters. A relationship with heritable fragile sites.
Venkatraj VS; Verma RS
Gynecol Obstet Invest; 1987; 24(4):241-9. PubMed ID: 3428712
[TBL] [Abstract][Full Text] [Related]
10. Fragile sites and spontaneous abortions.
Toncheva D
Genet Couns; 1991; 2(4):205-10. PubMed ID: 1799417
[TBL] [Abstract][Full Text] [Related]
11. No statistical association between common fragile sites and nonrandom chromosome breakpoints in cancer cells.
Sutherland GR; Simmers RN
Cancer Genet Cytogenet; 1988 Mar; 31(1):9-15. PubMed ID: 3162194
[TBL] [Abstract][Full Text] [Related]
12. Fragile sites and chromosome breakpoints in constitutional rearrangements.
Hecht F; Hecht BK
Clin Genet; 1985 Jul; 28(1):94. PubMed ID: 4028508
[No Abstract] [Full Text] [Related]
13. Distribution of X-ray-induced chromosome breakpoints in Down syndrome lymphocytes.
Shafik HM; Au WW; Whorton EB; Legator MS
Am J Med Genet Suppl; 1990; 7():195-200. PubMed ID: 2149946
[TBL] [Abstract][Full Text] [Related]
14. Use of fluorescence in situ hybridization to confirm the interpretation of a balanced complex chromosome rearrangement ascertained through prenatal diagnosis.
Wang H; McLaughlin M; Thompson C; Hunter AG
Am J Med Genet; 1993 Jun; 46(5):559-62. PubMed ID: 8322821
[TBL] [Abstract][Full Text] [Related]
15. Spontaneous chromosome aberrations in Fanconi's anemia patients are located at fragile sites and acute myeloid leukemia breakpoints.
Fundia A; Gorla N; Larripa I
Hereditas; 1994; 120(1):47-50. PubMed ID: 8206783
[TBL] [Abstract][Full Text] [Related]
16. A method for testing the nonrandomness of chromosomal breakpoints.
Tai JJ; Hou CD; Wang-Wuu S; Wang CH; Leu SY; Wuu KD
Cytogenet Cell Genet; 1993; 63(3):147-50. PubMed ID: 8485989
[TBL] [Abstract][Full Text] [Related]
17. Noninvolvement of a constitutional heritable fragile site at 10q24.2 in rearranged chromosomes from rectal carcinoma cells.
Muleris M; Dutrillaux AM; Lombard M; Dutrillaux B
Cancer Genet Cytogenet; 1987 Mar; 25(1):7-13. PubMed ID: 3467833
[TBL] [Abstract][Full Text] [Related]
18. Chromosome breakage and recombination at fragile sites.
Glover TW; Stein CK
Am J Hum Genet; 1988 Sep; 43(3):265-73. PubMed ID: 3137811
[TBL] [Abstract][Full Text] [Related]
19. The distribution of MspI-induced breaks in human lymphocyte chromosomes and its relationship to common fragile sites.
Porfirio B; Tedeschi B; Vernole P; Caporossi D; Nicoletti B
Mutat Res; 1989 Aug; 213(2):117-24. PubMed ID: 2474762
[TBL] [Abstract][Full Text] [Related]
20. De novo balanced chromosome rearrangements and extra marker chromosomes identified at prenatal diagnosis: clinical significance and distribution of breakpoints.
Warburton D
Am J Hum Genet; 1991 Nov; 49(5):995-1013. PubMed ID: 1928105
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]