108 related articles for article (PubMed ID: 6452750)
1. [Satellite associations in trisomy 21 (author's transl)].
Wachtler F; Andrle M; Rett A
Wien Klin Wochenschr; 1981 Jan; 93(1):13-6. PubMed ID: 6452750
[TBL] [Abstract][Full Text] [Related]
2. [Satellite association in two trisomic cases of Down's syndrome and in one healthy mother, with acrocentric variants (author's transl)].
Moreira LM; Ferrari I
Rev Bras Pesqui Med Biol; 1977 Jun; 10(3):187-91. PubMed ID: 142268
[TBL] [Abstract][Full Text] [Related]
3. [On the origin of meiotic errors with special reference to trisomy 21 (author's transl)].
Wagenbichler P
Wien Klin Wochenschr Suppl; 1976; 63():1-23. PubMed ID: 136814
[TBL] [Abstract][Full Text] [Related]
4. [Sex differences in the frequency of individual acrocentric chromosome association in short-term human lymphocyte cultures].
Kovaleva NV; Palkina TB
Tsitol Genet; 1980; 14(6):31-6. PubMed ID: 7466918
[TBL] [Abstract][Full Text] [Related]
5. Parental origin, nondisjunction, and recombination of the extra chromosome 21 in Down syndrome: a study in a sample of the Colombian population.
Ramírez NJ; Belalcázar HM; Yunis JJ; Quintero LN; Arboleda GH; Arboleda H
Biomedica; 2007 Mar; 27(1):141-8. PubMed ID: 17546231
[TBL] [Abstract][Full Text] [Related]
6. Parental origin and meiotic stage of non-disjunction in 139 cases of trisomy 21.
Ballesta F; Queralt R; Gómez D; Solsona E; Guitart M; Ezquerra M; Moreno J; Oliva R
Ann Genet; 1999; 42(1):11-5. PubMed ID: 10214502
[TBL] [Abstract][Full Text] [Related]
7. [Occurrence of an extra chromosome marker in persons with normal phenotype (author's transl)].
Mataszewska K; Mazurczak T; Stolarska A
Probl Med Wieku Rozwoj; 1977; 7():160-8. PubMed ID: 149307
[No Abstract] [Full Text] [Related]
8. [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]
9. Non-disjunction of chromosome 21, alphoid DNA variation, and sociogenetic features of Down syndrome.
Vorsanova SG; Iourov IY; Beresheva AK; Demidova IA; Monakhov VV; Kravets VS; Bartseva OB; Goyko EA; Soloviev IV; Yurov YB
Tsitol Genet; 2005; 39(6):30-6. PubMed ID: 16396318
[TBL] [Abstract][Full Text] [Related]
10. The origin of human trisomy: a study of heteromorphisms and satellite associations.
Jacobs PA; Mayer M
Ann Hum Genet; 1981 Oct; 45(4):357-65. PubMed ID: 6211127
[TBL] [Abstract][Full Text] [Related]
11. [Satellite chromosome associations in normal humans and in Down's syndrome].
Zhdanova NS
Tsitologiia; 1971 Jan; 13(1):42-50. PubMed ID: 4253662
[No Abstract] [Full Text] [Related]
12. [Frequency of Ag-stained NOR and satellite associations in four 14/21 translocation carriers and in their normal relatives (author's transl)].
Carnevale A; Blanco B; Dora Moya J
Rev Invest Clin; 1981; 33(4):365-8. PubMed ID: 6173908
[No Abstract] [Full Text] [Related]
13. Susceptible chiasmate configurations of chromosome 21 predispose to non-disjunction in both maternal meiosis I and meiosis II.
Lamb NE; Freeman SB; Savage-Austin A; Pettay D; Taft L; Hersey J; Gu Y; Shen J; Saker D; May KM; Avramopoulos D; Petersen MB; Hallberg A; Mikkelsen M; Hassold TJ; Sherman SL
Nat Genet; 1996 Dec; 14(4):400-5. PubMed ID: 8944019
[TBL] [Abstract][Full Text] [Related]
14. [Human acrocentric chromosomal associations in old age].
Lezhava TA
Tsitol Genet; 1979; 13(6):481-5. PubMed ID: 552667
[TBL] [Abstract][Full Text] [Related]
15. [A study on chromosomal satellite association in Down's syndrome and in the parents (author's transl)].
Chuang SM
Taiwan Yi Xue Hui Za Zhi; 1980 Jun; 79(6):533-41. PubMed ID: 6448909
[No Abstract] [Full Text] [Related]
16. Maternal age and origin of non-disjunction in trisomy 21.
Mattei JF; Ayme S; Mattei MG; Giraud F
J Med Genet; 1980 Oct; 17(5):368-72. PubMed ID: 6452525
[TBL] [Abstract][Full Text] [Related]
17. [Preferential segregation of chromosome 21p- in 3 generations. Ultimate role in non-disjunction (apropos of a case of trisomy 21 in this family)].
De los Cobos L; Ligia AP
J Genet Hum; 1981 Feb; 28(5):201-6. PubMed ID: 6456329
[TBL] [Abstract][Full Text] [Related]
18. [Restriction fragment length polymorphisms in the families of patients with Down's syndrome (trisomy 21)].
Mazura I; Horínek A; Franková Y; Kapras J
Cas Lek Cesk; 1993 Nov; 132(21):645-8. PubMed ID: 7903597
[TBL] [Abstract][Full Text] [Related]
19. Cell cycle analysis and properties of two sub-populations in PHA responding lymphocytes. A comparison of 21-trisomic and normal cells.
Kishi K
Jinrui Idengaku Zasshi; 1977 Jun; 22(1):17-26. PubMed ID: 144809
[No Abstract] [Full Text] [Related]
20. Parental origin of the extra chromosome in Down's Syndrome.
Mikkelsen M
J Ment Defic Res; 1982 Sep; 26(Pt 3):143-51. PubMed ID: 6217343
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]