150 related articles for article (PubMed ID: 2953898)
1. Structural rearrangements in the parents of children with primary trisomy 21.
Couzin DA; Watt JL; Stephen GS
J Med Genet; 1987 May; 24(5):280-2. PubMed ID: 2953898
[TBL] [Abstract][Full Text] [Related]
2. Pericentric inversions of chromosome 12 in two families.
Prieto F; Badía L; Asensi F; Moya A; Figuera MJ
Hum Genet; 1981; 57(2):131-3. PubMed ID: 6453076
[TBL] [Abstract][Full Text] [Related]
3. [Frequency of mixoploidy in 85 index cases with Down syndrome].
Armendares S; Buentellos L; Salamanca F
Rev Invest Clin; 1990; 42(2):103-7. PubMed ID: 2148432
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. Trisomy 21 Down syndrome. II. Structural chromosome rearrangements in the parents.
Uchida IA; Freeman VC
Hum Genet; 1986 Feb; 72(2):118-22. PubMed ID: 2935479
[TBL] [Abstract][Full Text] [Related]
6. Inv21p12q22del21q22 and intellectual disability.
Oliveira R; Dória S; Madureira C; Lima V; Almeida C; Pinho MJ; Ramalho C; Matoso E; Barros A; Carreira IM; Moura CP
Gene; 2013 Mar; 517(1):120-4. PubMed ID: 23266646
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. [Cytogenetic findings in patients with Down's syndrome].
Cortés F; Alliende M; Curotto B
Rev Chil Pediatr; 1990; 61(6):313-6. PubMed ID: 2152215
[TBL] [Abstract][Full Text] [Related]
9. Cytogenetic findings in leukemic cells of 56 patients with constitutional chromosome abnormalities. A cooperative study. Groupe Français de Cytogénétique Hématologique.
Cancer Genet Cytogenet; 1988 Oct; 35(2):243-52. PubMed ID: 2972356
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. [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]
12. [Cytogenetic study of the parents of 85 index cases with regular trisomy 21].
Armendares S; Buentello L; Salamanca F
Rev Invest Clin; 1990; 42(3):180-8. PubMed ID: 2148633
[TBL] [Abstract][Full Text] [Related]
13. [Structural chromosomal reorganizations and mosaicism in the parents of children with Down's syndrome].
Butomo IV; Kovaleva NV
Tsitol Genet; 1993; 27(1):87-91. PubMed ID: 8316960
[TBL] [Abstract][Full Text] [Related]
14. [Identification of families with increased risk of Down's syndrome caused by translocation of chromosome 9].
Rogóyski A; Babel M
Pediatr Pol; 1989 Apr; 64(4):209-15. PubMed ID: 2534166
[TBL] [Abstract][Full Text] [Related]
15. The prevalence of translocations in parents of children with regular trisomy 21: a possible interchromosomal effect?
Lindenbaum RH; Hultén M; McDermott A; Seabright M
J Med Genet; 1985 Feb; 22(1):24-8. PubMed ID: 3156995
[TBL] [Abstract][Full Text] [Related]
16. Six cases of partial duplication-deficiency 21 syndrome: 21(dupq22delp23) due to maternal pericentric inversion: inv(21)(p12;q22). A family study.
Fraisse J; Philip T; Bertheas MF; Lauras B
Ann Genet; 1986; 29(3):177-80. PubMed ID: 2947533
[TBL] [Abstract][Full Text] [Related]
17. Familial D-D translocation. A family showing transmission through three generations; a case with multiple congenital malformations, and a case of regular 21-trisomic Down's syndrome.
Visfeldt J
Acta Pathol Microbiol Scand; 1969; 75(4):545-54. PubMed ID: 4246134
[No Abstract] [Full Text] [Related]
18. The occurrence of a ring 18, an accessory bisatellited fragment, and trisomy 21 within one sibship.
Grace E; Sills J
Hum Genet; 1978 Jul; 43(1):111-4. PubMed ID: 149756
[TBL] [Abstract][Full Text] [Related]
19. Prenatal exclusion of segmental trisomy in familial chromosome 21 pericentric inversion by fluorescence in situ hybridization.
Tardy EP; Tóth A; Kosztolányi G
Prenat Diagn; 1997 Sep; 17(9):871-3. PubMed ID: 9316133
[TBL] [Abstract][Full Text] [Related]
20. Comparative analysis of the rates of chromosome damage induced by bleomycin radiomimetic in human trisomic and diploid lymphocytes: in vitro cultures from a mosaic of a Down's syndrome individual.
Cano J; Caparros MM; Pretel A
Cytobios; 1995; 83(334):159-66. PubMed ID: 8620688
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]