487 related articles for article (PubMed ID: 6217717)
1. 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]
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. Inherited pericentric inversion of Y-chromosome with trisomy 21. A case report.
Krishna Murthy DS; Murthy SK; Patel JK; Banker GN; Shah VC
Ann Genet; 1989; 32(1):47-51. PubMed ID: 2526612
[TBL] [Abstract][Full Text] [Related]
4. Beckwith-Wiedemann syndrome due to 11p15.5 paternal duplication associated with Klinefelter syndrome and a "de novo" pericentric inversion of chromosome Y.
Delicado A; Lapunzina P; Palomares M; Molina MA; Galán E; López Pajares I
Eur J Med Genet; 2005; 48(2):159-66. PubMed ID: 16053907
[TBL] [Abstract][Full Text] [Related]
5. A boy with trisomic Down's syndrome and a familial 5-?7 translocation, 47,XY,+21, t (5q-; ?7p+).
Yanagisawa S
Jinrui Idengaku Zasshi; 1972 Sep; 17(1):38-43. PubMed ID: 4265909
[No Abstract] [Full Text] [Related]
6. De novo tandem duplication of the middle segment of the long arm of chromosome 14.
Ito M; Mutoh K; Okuno T; Mikawa H; Edagawa J; Abe T
Ann Genet; 1983; 26(2):116-9. PubMed ID: 6604486
[TBL] [Abstract][Full Text] [Related]
7. Maternal balanced translocation (4;21) leading to an offspring with partial duplication of 4q and 21q without phenotypic manifestations of Down syndrome.
El-Ruby M; Hemly NA; Zaki MS
Genet Couns; 2007; 18(2):217-26. PubMed ID: 17710874
[TBL] [Abstract][Full Text] [Related]
8. [Chromosome analyses in parents of children with trisomy 21[].
Mattei JF; Giraud F
J Genet Hum; 1975 Oct; 23 SUPPL():31-41. PubMed ID: 129538
[TBL] [Abstract][Full Text] [Related]
9. Trisomy-21 in mother and child. Report of a case.
Friedman JM; Sternberg WH; Varela M; Barclay DL
Obstet Gynecol; 1970 Nov; 36(5):731-4. PubMed ID: 4248734
[No Abstract] [Full Text] [Related]
10. [Report on a case of Down's syndrome with mosaicism. Trisomy 21-normal, clearly mongoloid phenotype and normal iliac index in a newborn infant].
De Prà M; Lunetta Q
Minerva Pediatr; 1974 Jan; 26(2):78-81. PubMed ID: 4276194
[No Abstract] [Full Text] [Related]
11. [The intelligence level in the chromosome aberrations affecting autosomes].
Moor L
Rev Neuropsychiatr Infant; 1970 Dec; 18(12):943-66. PubMed ID: 4251821
[No Abstract] [Full Text] [Related]
12. [Partial trisomy for the segment 21(q11----qter) resulting from a de novo translocation between chromosomes 5 and 21].
Crippa L; Ballaman J; Engel E
Ann Genet; 1984; 27(3):190-3. PubMed ID: 6239590
[TBL] [Abstract][Full Text] [Related]
13. Inverted tandem ("mirror") duplications in human chromosomes: -nv dup 8p, 4q, 22q.
Taylor KM; Francke U; Brown MG; George DL; Kaufhold M
Am J Med Genet; 1977; 1(1):3-19. PubMed ID: 610424
[TBL] [Abstract][Full Text] [Related]
14. Clinical, cytogenetic, and molecular characterization of a girl with some clinical features of Down syndrome resulting from a pure partial trisomy 21q22.11-qter due to a de novo intrachromosomal duplication.
Vaglio A; Milunsky A; Quadrelli A; Huang XL; Maher T; Mechoso B; Martínez S; Pagano S; Bellini S; Costabel M; Quadrelli R
Genet Test Mol Biomarkers; 2010 Feb; 14(1):57-65. PubMed ID: 20143912
[TBL] [Abstract][Full Text] [Related]
15. [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]
16. [Double trisomy and transmitted pericentric inversion (48,XXY, +21,inv(22)). Interchromosomal effect].
Saura R; Longy M; Sautarael M; Renouil M; Sandler B
Ann Genet; 1983; 26(3):180-2. PubMed ID: 6606381
[TBL] [Abstract][Full Text] [Related]
17. Familial robertsonian translocation 15;21 and rare paracentric inv(21): unexpected re-inversion in a child with translocation trisomy 21.
Mau UA; Petruch UR; Kaiser P; Eggermann T
Eur J Hum Genet; 2000 Nov; 8(11):815-9. PubMed ID: 11093270
[TBL] [Abstract][Full Text] [Related]
18. [t(7q-; 21q-plus) and familial and trisomy 21].
Giraud F; Hartung M; Mattei JF; Mattie MG
Ann Genet; 1974 Mar; 17(1):49-53. PubMed ID: 4276449
[No Abstract] [Full Text] [Related]
19. Pure duplication 21q21.2-->qter due to a rea(21) in a Down syndrome girl. Remarks on nomenclature.
Dominguez MG; Arteaga-Alcaraz G; Rivera H
Genet Couns; 2012; 23(2):313-8. PubMed ID: 22876592
[TBL] [Abstract][Full Text] [Related]
20. Studies on sex-dimorphism of peripheral blood neutrophils in the langdon-down syndrome.
Dobrzańska A; Gajewska E
Pol Med J; 1968; 7(5):1130-6. PubMed ID: 4238324
[No Abstract] [Full Text] [Related]
[Next] [New Search]