401 related articles for article (PubMed ID: 8957510)
1. 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]
2. De novo (15;21) unbalanced translocation of paternal origin in a girl with Prader-Willi syndrome.
Cuoco C; Bicocchi MP; Granata D; Mezzano P; Serra G
Am J Med Genet; 1990 Sep; 37(1):62-4. PubMed ID: 2240045
[TBL] [Abstract][Full Text] [Related]
3. Segregation of a paternal insertional translocation results in partial 4q monosomy or 4q trisomy in two siblings.
Hegmann KM; Spikes AS; Orr-Urtreger A; Shaffer LG
Am J Med Genet; 1996 Jan; 61(1):10-5. PubMed ID: 8741910
[TBL] [Abstract][Full Text] [Related]
4. Prenatal diagnosis of partial monosomy 18p(18p11.2-->pter) and trisomy 21q(21q22.3-->qter) with alobar holoprosencephaly and premaxillary agenesis.
Chen CP; Chern SR; Wang W; Lee CC; Chen WL; Chen LF; Chang TY; Tzen CY
Prenat Diagn; 2001 May; 21(5):346-50. PubMed ID: 11360273
[TBL] [Abstract][Full Text] [Related]
5. Variable expression of phenotype in offspring with partial monosomy 7q and partial trisomy 8p in a family with a rcp (7;8)(134;p12) translocation.
Frints SG; Moerman P; Fryns JP
Genet Couns; 1996; 7(4):313-9. PubMed ID: 8985736
[TBL] [Abstract][Full Text] [Related]
6. [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]
7. Spectral karyotyping and fluorescence in situ hybridization analysis of de novo partial trisomy 7p (7p21.2-->pter) and partial monosomy 12q (12q24.33-->qter).
Chen CP; Lin SP; Lin CC; Li YC; Hsieh LJ; Huang JK; Lee CC; Wang W
Genet Couns; 2006; 17(1):57-63. PubMed ID: 16719278
[TBL] [Abstract][Full Text] [Related]
8. Proximal trisomy 13q and distal monosomy 8p in a dysmorphic and mentally retarded patient with an isodicentric chromosome 13q and a 13q/8p translocation chromosome.
Lukusa T; van den Berghe L; Smeets E; Fryns JP
Ann Genet; 1999; 42(4):215-20. PubMed ID: 10674161
[TBL] [Abstract][Full Text] [Related]
9. Partial trisomy 4q and monosomy 9p resulting from a familial translocation t(4;9)(q27;p24) in a child with choanal atresia.
Wouters CH; van Bodegom TM; Moll HA; Govaerts LC
Ann Genet; 1999; 42(3):160-5. PubMed ID: 10526659
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. [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]
12. [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]
13. Chromosomal abnormalities and glaucoma: a case of congenital glaucoma with trisomy 8q22-qter/ monosomy 9p23-pter.
Cohn AC; Kearns LS; Savarirayan R; Ryan J; Craig JE; Mackey DA
Ophthalmic Genet; 2005 Mar; 26(1):45-53. PubMed ID: 15823925
[TBL] [Abstract][Full Text] [Related]
14. Prenatal findings and molecular cytogenetic analyses of partial trisomy 12q (12q24.32-->qter) and partial monosomy 21q (21q22.2-->qter).
Chen CP; Chern SR; Lin CC; Wang TH; Li YC; Hsieh LJ; Lee CC; Hua HM; Wang W
Prenat Diagn; 2006 Apr; 26(4):313-20. PubMed ID: 16506269
[TBL] [Abstract][Full Text] [Related]
15. Unbalanced 18q/21q translocation in a patient previously reported as monosomy 21.
Riegel M; Hargreaves P; Baumer A; Guc-Scekic M; Ignjatovic M; Schinzel A
Eur J Med Genet; 2005; 48(2):167-74. PubMed ID: 16053908
[TBL] [Abstract][Full Text] [Related]
16. Non-reciprocal translocation (5;15), isodicentric (15) and Prader-Willi syndrome.
Murdock RL; Wurster-Hill DH
Am J Med Genet; 1986 Sep; 25(1):61-9. PubMed ID: 3799724
[TBL] [Abstract][Full Text] [Related]
17. Monosomy 9p24-->pter and trisomy 5q31-->qter: case report and review of two cases.
Schimmenti LA; Higgins RR; Mendelsohn NJ; Casey TM; Steinberger J; Mammel MC; Wiesner GL
Am J Med Genet; 1995 May; 57(1):52-6. PubMed ID: 7645598
[TBL] [Abstract][Full Text] [Related]
18. Partial trisomy 17q and monosomy 9p due to a familial translocation.
Cotter PD; Stewart NL
Ann Genet; 1990; 33(4):231-3. PubMed ID: 1710432
[TBL] [Abstract][Full Text] [Related]
19. Two cases of partial trisomy 10q syndrome due to a familial 10;20 translocation.
Tüysüz B; Hacihanefioglu S; Silahtaroglu A; Yilmaz S; Deviren A; Cenani A
Genet Couns; 2000; 11(4):355-61. PubMed ID: 11140413
[TBL] [Abstract][Full Text] [Related]
20. Molecular and cytogenetic characterization of a recurrent unbalanced translocation (4;21)(p16.3;q22.1): relevance to the Wolf-Hirschhorn and Down syndrome critical regions.
Sebastio G; Perone L; Guzzetta V; Sebastio L; Vicari L; Della Casa R; Gurrieri F; Zappata S; Pomponi MG; Mazzei A; Neri G; Andria G; Brahe C
Am J Med Genet; 1996 May; 63(2):366-72. PubMed ID: 8725787
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
