208 related articles for article (PubMed ID: 9182774)
21. [Translocation trisomy 4q in 2 siblings as a sequela of paternal balanced reciprocal translocation: t(1;4)(q44;q31)].
Bode H; Bühler EM; Wyler F; Hadzilselimovic F
Monatsschr Kinderheilkd; 1990 Nov; 138(11):763-6. PubMed ID: 2290435
[TBL] [Abstract][Full Text] [Related]
22. De novo unbalanced t(11q;21q) leading to a partial monosomy 21pter-q22.2 and 11q24-qter in a patient initially diagnosed as monosomy 21.
Riegel M; Baumer A; Piram A; Ortolan D; Peres LC; Pina-Neto JM
Genet Couns; 2001; 12(1):69-75. PubMed ID: 11332980
[TBL] [Abstract][Full Text] [Related]
23. Partial trisomy (11;22) syndrome with manifestations of Goldenhar sequence due to maternal balanced t(11;22).
Balci S; Engiz O; Yilmaz Z; Baltaci V
Genet Couns; 2006; 17(3):281-9. PubMed ID: 17100195
[TBL] [Abstract][Full Text] [Related]
24. 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]
25. [Marker chromosomes as a product of familial translocation (11;22) identified with molecular cytogenetic methods].
Stankiewicz P; Korniszewski L; Bocian E; Stańczak H
Pediatr Pol; 1996 Mar; 71(3):241-5. PubMed ID: 8966096
[TBL] [Abstract][Full Text] [Related]
26. A family with segregation of an unbalanced translocation (7;13) (q36;q32) in three patients with severe mental retardation, microcephaly and dysmorphic features, detected by subtelomere FISH: genetic counselling and prenatal diagnosis.
Nucaro A; Crisponi G; Minafra L; Rossino R; Cianchetti C
Genet Couns; 2008; 19(1):37-42. PubMed ID: 18564499
[TBL] [Abstract][Full Text] [Related]
27. Combined trisomy 9 and Ullrich-Turner syndrome in a girl with a 46,X,der(9)t(X;9)(q12;q32) karyotype.
Canún S; Mutchinick O; Shaffer LG; Fernández C
Am J Med Genet; 1998 Nov; 80(3):199-203. PubMed ID: 9843037
[TBL] [Abstract][Full Text] [Related]
28. Congenital glaucoma and Silver-Russell phenotype associated with partial trisomy 7q and monosomy 15q.
Kato R; Kishibayashi J; Shimokawa O; Harada N; Niikawa N; Matsumoto N
Am J Med Genet; 2001 Dec; 104(4):319-22. PubMed ID: 11754068
[TBL] [Abstract][Full Text] [Related]
29. [Cytogenetic and molecular characterization of partial trisomy 4q and partial monosomy 10q in a patient].
Zhang YL; Dai Y; Tu ZG; Li QY; Wang LQ; Zhang L; Zeng J; Ouyang ZB
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2010 Apr; 27(2):153-7. PubMed ID: 20376795
[TBL] [Abstract][Full Text] [Related]
30. Partial trisomy and partial monosomy of the distal long arm of chromosome 4: patient report and literature review.
Frints SG; Schrander-Stumpel CT; Engelen JJ; Da Costa AJ; Fryns JP
Genet Couns; 1996; 7(2):135-42. PubMed ID: 8831133
[TBL] [Abstract][Full Text] [Related]
31. Partial monosomy 2p and partial trisomy 4q due to paternal translocation t(2;4)(p25.1;q31.3).
Skrlec I; Wagner J; Puseljić S; Heffer M; Stipoljev F
Coll Antropol; 2014 Jun; 38(2):759-62. PubMed ID: 25145019
[TBL] [Abstract][Full Text] [Related]
32. 'Pure' partial trisomy 4q26-->q35.2 resulting from a familial unbalanced translocation t(4;10)(q26;q26.3).
Zhang YL; Dai Y; Tu ZG; Li QY
Cytogenet Genome Res; 2009; 127(1):67-72. PubMed ID: 20145385
[TBL] [Abstract][Full Text] [Related]
33. Two craniosynostotic patients with 11q deletions, and review of 48 cases.
Lewanda AF; Morsey S; Reid CS; Jabs EW
Am J Med Genet; 1995 Nov; 59(2):193-8. PubMed ID: 8588585
[TBL] [Abstract][Full Text] [Related]
34. 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]
35. Coexistent mosaic monosomy 21 and fragile X syndrome in a mentally retarded male patient.
Utine GE; Aktas D; Boduroğlu K; Alikasifoğlu M; Tunçbilek E
Genet Couns; 2007; 18(2):171-7. PubMed ID: 17710869
[TBL] [Abstract][Full Text] [Related]
36. Further contribution to the description of phenotypes associated with partial 4q duplication.
Zollino M; Zampino G; Torrioli G; Pomponi MG; Neri G
Am J Med Genet; 1995 May; 57(1):69-73. PubMed ID: 7645603
[TBL] [Abstract][Full Text] [Related]
37. [Partial trisomy 11q 46, XX, 4q+ by translocation t (4; 11) (q35; q12)].
Le Chevalier C; Chabrolle JP; Rossier A
Ann Pediatr (Paris); 1978 Nov; 25(9):501-4, 507. PubMed ID: 16114368
[No Abstract] [Full Text] [Related]
38. Molecular characterization of partial trisomy 16q24.1-qter: clinical report and review of the literature.
Brisset S; Joly G; Ozilou C; Lapierre JM; Gosset P; LeLorc'h M; Raoul O; Turleau C; Vekemans M; Romana SP
Am J Med Genet; 2002 Dec; 113(4):339-45. PubMed ID: 12457405
[TBL] [Abstract][Full Text] [Related]
39. Confirmation of a cryptic unbalanced translocation using whole chromosome fluorescence in situ hybridization.
Mewar R; Kline AD; Jackson L; Overhauser J
Am J Med Genet; 1992 Nov; 44(4):477-81. PubMed ID: 1442891
[TBL] [Abstract][Full Text] [Related]
40. Mosaic rearrangement of chromosome 18: characterization by FISH mapping and DNA studies shows trisomy 18p and monosomy 18p both of paternal origin.
Oner G; Jauch A; Eggermann T; Hardwick R; Kirsch S; Schiebel K; Rappold G; Robson L; Smith A
Am J Med Genet; 2000 May; 92(2):101-6. PubMed ID: 10797432
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
