272 related articles for article (PubMed ID: 9475102)
1. Partial trisomy 1(q42-->qter): a new case with a mild phenotype.
Concolino D; Cinti R; Ferraro L; Moricca MT; Strisciuglio P
J Med Genet; 1998 Jan; 35(1):75-7. PubMed ID: 9475102
[TBL] [Abstract][Full Text] [Related]
2. Inv dup del (1)(pter-->q44::q44-->q42:) with the classical phenotype of trisomy 1q42-qter.
De Brasi D; Rossi E; Giglio S; D'Agostino A; Titomanlio L; Farina V; Andria G; Sebastio G
Am J Med Genet; 2001 Nov; 104(2):127-30. PubMed ID: 11746042
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. Pure 9p trisomy derived from a terminal balanced unreciprocal translocation.
Brambila-Tapia AJ; Neira VA; Vásquez-Velásquez AI; Jimenez-Arredondo RE; Chávez-González EL; Picos-Cárdenas VJ; Fletes-Rayas AL; Figuera LE
Genet Couns; 2014; 25(3):289-97. PubMed ID: 25365851
[TBL] [Abstract][Full Text] [Related]
5. Partial monosomy 8q and partial trisomy 9q due to the maternal translocation t(8;9(q24.3;q34.1): a case report.
Tos T; Alp MY; Eker HK; Cebi AH; Ikbal M
Genet Couns; 2014; 25(1):35-9. PubMed ID: 24783653
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. Clinical and molecular cytogenetic characterization of two patients with partial trisomy 1q41-qter: further delineation of partial trisomy 1q syndrome.
Emberger W; Petek E; Kroisel PM; Zierler H; Wagner K
Am J Med Genet; 2001 Dec; 104(4):312-8. PubMed ID: 11754067
[TBL] [Abstract][Full Text] [Related]
8. An unusual clinical characterization of a male with distal partial trisomy 1q42.1 and monosomy 4q35.1 and review of the literature.
Wang CB; Lin SP; Chen CP; Chen YJ; Lee CC
Genet Couns; 2006; 17(4):435-40. PubMed ID: 17375530
[TBL] [Abstract][Full Text] [Related]
9. Precocious puberty associated with partial trisomy 18q and monosomy 11q.
Mutesa L; Hellin AC; Jamar M; Pierquin G; Bours V; Verloes A
Genet Couns; 2007; 18(2):201-7. PubMed ID: 17710872
[TBL] [Abstract][Full Text] [Related]
10. Partial trisomy 1q (1q42.13-->qter) and partial monosomy 6q (6q27-->qter) in a girl with single median maxillary central incisor, corpus callosum dysgenesis and developmental delay.
Chen CP; Lin SP; Su YN; Chern SR; Su JW; Lee CC; Wang W
Genet Couns; 2012; 23(4):447-55. PubMed ID: 23431743
[TBL] [Abstract][Full Text] [Related]
11. 1q44-qter trisomy: clinical report and review of the literature.
Lenzini E; Ballarati L; Drigo P; Carrozzi M; Gambel-Benussi D; Giardino D; Petix V; Rizzotto MR; Pecile V
Genet Test Mol Biomarkers; 2009 Feb; 13(1):79-86. PubMed ID: 19309278
[TBL] [Abstract][Full Text] [Related]
12. Further clinical delineation in trisomy 1q32 syndrome.
Nuño-Arana I; González-García JR; García-Cruz D
Ann Genet; 2001; 44(4):175-7. PubMed ID: 11755100
[TBL] [Abstract][Full Text] [Related]
13. A severely mental and motor retarded boy with monosomy 9pter-->p22 trisomy 10q26-->qter due to paternal reciprocal translocation 46,XY,t(9;10)(p23;q26).
Akbas E; Polat S; Karakas-Celik S; Altintas ZM; Yildirim M; Yilgor E
Genet Couns; 2011; 22(4):417-23. PubMed ID: 22303803
[TBL] [Abstract][Full Text] [Related]
14. Attenuated phenotype in a child with trisomy for 1q due to unbalanced X;1 translocation [46,X,der(X),t(X;1)(q28;q32.1)].
Yatsenko SA; Sahoo T; Rosenkranz M; Mendoza-Londono R; Naeem R; Scaglia F
Am J Med Genet A; 2004 Jul; 128A(1):72-7. PubMed ID: 15211662
[TBL] [Abstract][Full Text] [Related]
15. A severely mentally and motor retarded girl with monosomy 3pter-->p25 and trisomy 8q24-->qter due to a familial reciprocal translocation t(3;8)(p25;q24).
Balci S; Aypar E; Beksaç MS; Bartsch O
Genet Couns; 2009; 20(2):125-32. PubMed ID: 19650409
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. Inverted duplication of 1q32.1 to 1q44 characterized by array CGH and review of distal 1q partial trisomy.
Balasubramanian M; Barber JC; Collinson MN; Huang S; Maloney VK; Bunyan D; Foulds N
Am J Med Genet A; 2009 Feb; 149A(4):793-7. PubMed ID: 19248177
[No Abstract] [Full Text] [Related]
18. Clinical and molecular cytogenetic studies in a case with partial trisomy 12p due to a de novo supernumerary ring chromosome.
Ausems MG; Schuil J; Van Raveswaaij-Arts C; De Pater JM
Genet Couns; 2004; 15(4):405-10. PubMed ID: 15658615
[TBL] [Abstract][Full Text] [Related]
19. [Two cases of partial trisomy 8p derived from paternal reciprocal translocation or maternal insertion translocation: clinical features and genetic abnormalities].
Xiao B; Zhang JM; Ji X; Jiang WT; Hu J; Tao J
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2011 Jun; 28(3):247-50. PubMed ID: 21644216
[TBL] [Abstract][Full Text] [Related]
20. Phenotypic features of a boy with trisomy of 16q22-->qter due to paternal Y; 16 translocation.
Tsien F; Morava E; Talarski A; Marble M
Clin Dysmorphol; 2005 Oct; 14(4):177-181. PubMed ID: 16155418
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
