141 related articles for article (PubMed ID: 607844)
1. [Translocation t (13:21) (q22:q22) in mother and monosomia 21 and partial trisomy 13 on her son (author's transl)].
Prieto García F; Badía Garrabou L; Ferrer Calvette J
An Esp Pediatr; 1977 Dec; 10(12):927-32. PubMed ID: 607844
[TBL] [Abstract][Full Text] [Related]
2. [Partial trisomy (10pter leads to 10q21) and partial monosomy (21pter leads to 21q21) due to a reciprocal balanced familial translocation (10;21)(q21;q21) (author's transl)].
Obry E; Piussan C; Risbourg B; Dutrillaux B
Ann Genet; 1980; 23(4):216-20. PubMed ID: 6971599
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. [Increased activity of adenine phosphoribosyl transferase in a child trisomic for 16q22.2 to 16qter due to malsegregation of a t(16;21) (q22.2;q22;2)pat (author's transl)].
Rethoré MO; Lafourcade J; Couturier J; Harpey JP; Hamet M; Engler R; Alcindor LG; Lejeune J
Ann Genet; 1982; 25(1):36-42. PubMed ID: 6979298
[TBL] [Abstract][Full Text] [Related]
5. [Translocation 46,XX, t(15; 21) (q13; q22,1) in the mother of 2 children with partial trisomy 15 and monosomy 21].
Rethoré MO; Dutrillaux B
Ann Genet; 1973 Dec; 16(4):271-5. PubMed ID: 4544092
[No Abstract] [Full Text] [Related]
6. Partial trisomy 13 due to maternal translocation t(7;13)(p22q14).
Martin-Lucas MA; Pérez-Castillo A; Abrisqueta JA; de Torres ML; Martin-Sempere MJ; Del Mazo J; Aller V
Ann Genet; 1982; 25(3):172-8. PubMed ID: 6982670
[TBL] [Abstract][Full Text] [Related]
7. t(15;21)(q15;q22.1) pat resulting in partial trisomy and partial monosomy of chromosomes 15 and 21 in two offspring.
Abeliovich D; Dagan J; Lerer I; Silberstein S; Katznelson MB; Frydman M
Am J Med Genet; 1996 Dec; 66(1):45-51. PubMed ID: 8957510
[TBL] [Abstract][Full Text] [Related]
8. [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]
9. "Pure" monosomy 21 pter leads to q21 in a girl born to a couple 46,XX,t(14;21)(p12;q22) and 46,XY,t(5;18)(q32;q22).
Rivera H; Rivas F; Plascencia L; Cantú JM
Ann Genet; 1983; 26(4):234-7. PubMed ID: 6607704
[TBL] [Abstract][Full Text] [Related]
10. [Partial trisomy 13 for the distal long arm and its prenatal diagnosis].
Zolotukhina TV; Rozovskiĭ IS; Bartseva OB; Vakhlamova IV; Bubnova NI
Genetika; 1982 Nov; 18(11):1899-905. PubMed ID: 6891355
[TBL] [Abstract][Full Text] [Related]
11. [Partial trisomy 18 (pter leads to q122) of maternal origin (author's transl)].
Jaffray JY; Geneix A; Goumy P; Perissel B; Menut G; Malet P
Ann Genet; 1980; 23(4):224-7. PubMed ID: 6971601
[TBL] [Abstract][Full Text] [Related]
12. Translocation of 9q/13q resulting in duplication (trisomy 9pter leads to 9q22) and deficiency (monosomy 13pter leads to 13q12).
Howard-Peebles PN; Yarbrough KM; Stoddard GR; Rary JM
Clin Genet; 1977 Jan; 11(1):46-52. PubMed ID: 830449
[TBL] [Abstract][Full Text] [Related]
13. [T (14q-; 21q + ) translocation in the father. Partial trisomy 14 and monosomy 21 in the daughter].
Laurent C; Dutrillaux B; Biemont MC; Genoud J; Bethenod M
Ann Genet; 1973 Dec; 16(4):281-4. PubMed ID: 4544094
[No Abstract] [Full Text] [Related]
14. Partial monosomy 22pter leads to q11 in a newborn with the clinical features of trisomy 13 syndrome.
Back E; Stier R; Böhm N; Adlung A; Hameister H
Ann Genet; 1980; 23(4):244-8. PubMed ID: 6971606
[TBL] [Abstract][Full Text] [Related]
15. [Increased activity of adenine phosphoribosyl transferase in a child trisomic for 16q22.2 to 16qter due to malsegregation of a t(16;21) (q22.2;q22;2)pat].
Rethoré MO; Lafourcade J; Couturier J; Harpey JP; Hamet M; Engler R; Alcindor LG; Lejeune J
Sem Hop; 1982 Dec; 58(45):2639-45. PubMed ID: 6297060
[TBL] [Abstract][Full Text] [Related]
16. Unusual chromosome aberrations in 3 children with Down syndrome.
Osztovics M; Tóth S; Wilhelm O
Acta Paediatr Acad Sci Hung; 1982; 23(3):283-9. PubMed ID: 6217717
[TBL] [Abstract][Full Text] [Related]
17. [Partial trisomy of chromosome 21 by maternal translocation t(15;21) (q26.2; q21)].
Raoul O; Carpentier S; Dutrillaux B; Mallet R; Lejeune J
Ann Genet; 1976 Sep; 19(3):187-90. PubMed ID: 136225
[TBL] [Abstract][Full Text] [Related]
18. [Phenotypic disorders in balanced reciprocal translocation: karyotype 46,XY,rcp(13; 21)(q22; q22)].
Badalian LO; Malygina NA; Gozman TV; Petrukhin AS; Mutovin GR
Tsitol Genet; 1982; 16(2):17-21. PubMed ID: 7101445
[TBL] [Abstract][Full Text] [Related]
19. [Reciprocal syndromes caused by deficiency duplication resulting from maternal t(10;18)(p12;q22) translocation].
Rethoré MO; Prieur M; de Blois MC; Naffah J; Ravel A; Villain E; Lejeune J
Ann Genet; 1985; 28(3):149-53. PubMed ID: 3879147
[TBL] [Abstract][Full Text] [Related]
20. [Partial trisomy 11q;22q (author's transl)].
Benítez J; Ayuso C; García Aparicio J; Sáez E; Pérez Sotelo A; Bello MJ
An Esp Pediatr; 1981 Sep; 15(3):293-300. PubMed ID: 7332142
[No Abstract] [Full Text] [Related]
[Next] [New Search]
