109 related articles for article (PubMed ID: 2757360)
1. Partial trisomy 13q22----qter. A new case.
Galán F; García R; Aguilar MS; Moya M
Ann Genet; 1989; 32(2):114-6. PubMed ID: 2757360
[TBL] [Abstract][Full Text] [Related]
2. The phenotypic and cytogenetic spectrum of partial trisomy 9.
Wilson GN; Raj A; Baker D
Am J Med Genet; 1985 Feb; 20(2):277-82. PubMed ID: 3976721
[TBL] [Abstract][Full Text] [Related]
3. Trisomy for the short arm of chromosome 10. Report of a new case resulting from segregation of a maternal balanced translocation t(10qter----q11::14p11----qter).
Delaroche I; Bruni L; Giannotti A; Giampaolo R; Aebischer ML
Helv Paediatr Acta; 1984 May; 39(2):161-6. PubMed ID: 6543839
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. [Phenotype positioning on chromosomes in a patient with the syndrome of partial trisomy 7p21.2-->pter].
Liang DS; Wu LQ; Cai F; Xia K; Long ZG; Pan Q; Dai HP; Xia JH
Yi Chuan Xue Bao; 2005 Feb; 32(2):124-9. PubMed ID: 15759858
[TBL] [Abstract][Full Text] [Related]
6. De novo dir dup (1)(q3200----4200) in an adult. Further delineation of the pure 1q trisomy syndrome.
Barros-Núñez P; Sánchez-Corona J; Rolón A; Medina C; García-Ochoa C; García-Cruz MO; Nazará Z; García-Cruz D
Ann Genet; 1989; 32(2):97-101. PubMed ID: 2667459
[TBL] [Abstract][Full Text] [Related]
7. [Trisomy 11 q (q23.1 - qter) through maternal translocation t(11;22) (q23.1;q11.1). A new case].
Ayraud N; Galiana A; Llyod M; Deswarte M
Ann Genet; 1976 Mar; 19(1):65-8. PubMed ID: 1084126
[TBL] [Abstract][Full Text] [Related]
8. Trisomy 1q43 syndrome: a consistent phenotype with macrocephaly, characteristic face, developmental delay and cardiac anomalies.
Morava E; Jackson KE; Tsien F; Marble MR
Genet Couns; 2004; 15(4):449-53. PubMed ID: 15658621
[TBL] [Abstract][Full Text] [Related]
9. Partial trisomy of the distal part of 10q: a report of two Egyptian cases.
Aglan MS; Kamel AK; Helmy NA
Genet Couns; 2008; 19(2):199-209. PubMed ID: 18618995
[TBL] [Abstract][Full Text] [Related]
10. Trisomy 22 in a liveborn infant with multiple congenital anomalies.
McPherson E; Stetka DG
Am J Med Genet; 1990 May; 36(1):11-4. PubMed ID: 2333899
[TBL] [Abstract][Full Text] [Related]
11. Malformation syndrome of duplication 12q24.1 leads to qter.
Melnyk AR; Weiss L; Van Dyke DL; Jarvi P
Am J Med Genet; 1981; 10(4):357-65. PubMed ID: 7332029
[TBL] [Abstract][Full Text] [Related]
12. [A case of partial 6q trisomy diagnosed at birth].
Bartalena L; D'Accavio L; Pellegrinetti C; Tarantino E
Pathologica; 1990; 82(1081):549-52. PubMed ID: 2080100
[TBL] [Abstract][Full Text] [Related]
13. Blepharophimosis and mental retardation (BMR) phenotypes caused by chromosomal rearrangements: description in a boy with partial trisomy 10q and monosomy 4q and review of the literature.
Bartholdi D; Toelle SP; Steiner B; Boltshauser E; Schinzel A; Riegel M
Eur J Med Genet; 2008; 51(2):113-23. PubMed ID: 18262484
[TBL] [Abstract][Full Text] [Related]
14. A cryptic duplication 22q13.31 to qter leads to a distinct phenotype with mental retardation, microcephaly and mild facial dysmorphism.
Peeters H; Vermeesch J; Fryns JP
Genet Couns; 2008; 19(4):365-71. PubMed ID: 19239079
[TBL] [Abstract][Full Text] [Related]
15. Follow-up of a patient with partial trisomy 9p and partial monosomy 8p; description of physical and psychosocial development.
Ausems MG; Van Spijker HG; Dijkhuis HJ; Swanenburg De Veye HF; Bijlsma JB
Genet Couns; 1996; 7(1):61-5. PubMed ID: 8652090
[TBL] [Abstract][Full Text] [Related]
16. A case with laryngeal atresia and partial trisomy 9 due to maternal 9;16 translocation.
Van den Boogaard MJ; De Pater J; Hennekam RC
Genet Couns; 1991; 2(2):83-91. PubMed ID: 1781959
[TBL] [Abstract][Full Text] [Related]
17. Partial trisomy 13 in an infant with a mild phenotype: application of fluorescence in situ hybridization in cytogenetic syndromes.
Begovic D; Hitrec V; Lasan R; Letica L; Baric I; Sarnavka V; Galic S
Croat Med J; 1998 Jun; 39(2):212-5. PubMed ID: 9575279
[TBL] [Abstract][Full Text] [Related]
18. The 8p-syndrome.
Ostergaard GZ; Tommerup N
Ann Genet; 1989; 32(2):87-91. PubMed ID: 2667457
[TBL] [Abstract][Full Text] [Related]
19. Interstitial and terminal deletions of the long arm of chromosome 4: further delineation of phenotypes.
Lin AE; Garver KL; Diggans G; Clemens M; Wenger SL; Steele MW; Jones MC; Israel J
Am J Med Genet; 1988 Nov; 31(3):533-48. PubMed ID: 3067575
[TBL] [Abstract][Full Text] [Related]
20. An infant with Beckwith-Wiedemann syndrome and chromosomal duplication 11p13----pter.: correlation of symptoms between 11p trisomy and Beckwith-Wiedemann syndrome.
Okano Y; Osasa Y; Yamamoto H; Hase Y; Tsuruhara T; Fujita H
Jinrui Idengaku Zasshi; 1986 Dec; 31(4):365-72. PubMed ID: 3613243
[No Abstract] [Full Text] [Related]
[Next] [New Search]
