356 related articles for article (PubMed ID: 2149630)
1. Translocation (14;21)(q11;q22) in a woman with history of abortions and a child with Down's syndrome.
Sudha T; Gopinath PM
Ann Genet; 1990; 33(3):162-4. PubMed ID: 2149630
[TBL] [Abstract][Full Text] [Related]
2. [Multiple chromosome aberrations in 3 generations of a family and Down's syndrome resulting from partial trisomy of chromosome 21 (q21--q22)].
Butomo IV; Prozorova MV; Khitrikova LE
Tsitol Genet; 1984; 18(3):223-8. PubMed ID: 6235655
[TBL] [Abstract][Full Text] [Related]
3. [Frequency of chromosome variants in human populations].
Kuleshov NP; Kulieva LM
Genetika; 1979; 15(3):745-51. PubMed ID: 160358
[TBL] [Abstract][Full Text] [Related]
4. Down's syndrome. I. Cytogenetics.
Maximilian C; Duca D; Pop T; Toncescu N; Ioan D
Endocrinologie; 1980; 18(4):273-5. PubMed ID: 6451918
[TBL] [Abstract][Full Text] [Related]
5. Chromosome 21 behavior during fetal oogenesis in Down's syndrome.
Jagiello GM; Fang JS; Nogawa T; Sung WK; Ducayen MB; Bowne W
Obstet Gynecol; 1987 Dec; 70(6):878-83. PubMed ID: 2960924
[TBL] [Abstract][Full Text] [Related]
6. Homologous Robertsonian translocation (21q21q) and abortions.
Sudha T; Gopinath PM
Hum Genet; 1990 Jul; 85(2):253-5. PubMed ID: 2142474
[TBL] [Abstract][Full Text] [Related]
7. Cytogenetic studies in Down syndrome.
Verma IC; Mathew S; Elango R; Shukla A
Indian Pediatr; 1991 Sep; 28(9):991-6. PubMed ID: 1839389
[TBL] [Abstract][Full Text] [Related]
8. Mitotic disturbances associated with inversion 9qh. A case report.
Murthy SK; Prabhakara K
Ann Genet; 1990; 33(3):169-72. PubMed ID: 2149631
[TBL] [Abstract][Full Text] [Related]
9. Complex chromosomal rearrangement and multiple spontaneous abortions.
Gorski JL; Emanuel BS; Zackai EH; Mennuti M
Hum Genet; 1986 Nov; 74(3):326. PubMed ID: 3781562
[TBL] [Abstract][Full Text] [Related]
10. Postzygotic D/D translocation homozygosity associated with recurrent abortions.
Maeda T; Ohno M; Takada M; Matsunobu A; Arai M
Am J Med Genet; 1983 Jul; 15(3):389-92. PubMed ID: 6881208
[TBL] [Abstract][Full Text] [Related]
11. Inheritance of a translocation between chromosomes 12 and 16 in a family with recurrent miscarriages and a newborn with Down syndrome carrying the same translocation.
Pazarbaşi A; Demirhan O; Turgut M; Güzel I; Taştemir D
Genet Couns; 2008; 19(3):301-8. PubMed ID: 18990986
[TBL] [Abstract][Full Text] [Related]
12. Translocation t(22;22)(p11.1;q11.1) and NOR studies in a female with a history of repeated fetal loss.
Multani AS; Radhakrishna U; Sheth FJ; Shah VC; Chinoy NJ
Ann Genet; 1992; 35(2):105-9. PubMed ID: 1524406
[TBL] [Abstract][Full Text] [Related]
13. Down's syndrome and leukemia: mechanism of additional chromosomal abnormalities.
Goh K; Lee H; Miller G
Am J Ment Defic; 1978 May; 82(6):542-8. PubMed ID: 148844
[TBL] [Abstract][Full Text] [Related]
14. [Down's syndrome with unusual karyotype: iso-pseudo-dicentric chromosome 21].
Kosztolányi G
Orv Hetil; 1988 Mar; 129(10):501-2. PubMed ID: 2966331
[No Abstract] [Full Text] [Related]
15. 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]
16. A rare reciprocal translocation (12;21) segregating for nine generations.
Koskinen S; Onnelainen T; de la Chapelle A; Kere J
Hum Genet; 1993 Nov; 92(5):509-12. PubMed ID: 8244343
[TBL] [Abstract][Full Text] [Related]
17. [A case of familial paracentric inversion associated with Down's syndrome. 47, XX, +21, inv (1) (p22p36)].
Alonso Villa MJ; Plasencia Amela A; Hernando Acero I; Benavides Benavides A; Fernández Cuesta M; Fernández Toral J
An Esp Pediatr; 1990 Mar; 32(3):257-8. PubMed ID: 2140666
[No Abstract] [Full Text] [Related]
18. [Acrocentric chromosomal associations in the families of children with Down's disease].
Kovaleva NV; Butomo IV; Novikova IIu
Tsitologiia; 1993; 35(10):33-43. PubMed ID: 8165746
[TBL] [Abstract][Full Text] [Related]
19. [Heterochromatic regions and the nondisjunction of human chromosome 21. I. Polymorphism of the C-bands of chromosomes 1, 9 and 16 in children with Down's syndrome].
Podugol'nikova OA
Tsitologiia; 1987 Jun; 29(6):711-4. PubMed ID: 2957841
[TBL] [Abstract][Full Text] [Related]
20. [The associations of acrocentric chromosomes in the parents of Down's syndrome children (a review of the literature)].
Kovaleva NV
Tsitologiia; 1991; 33(6):3-11. PubMed ID: 1840366
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
