543 related articles for article (PubMed ID: 7802005)
1. Molecular cytogenetic determination of a deletion/duplication of 1q that results in a trisomy 18 syndrome-like phenotype.
Mewar R; Harrison W; Weaver DD; Palmer C; Davee MA; Overhauser J
Am J Med Genet; 1994 Aug; 52(2):178-83. PubMed ID: 7802005
[TBL] [Abstract][Full Text] [Related]
2. Two patients with overlapping de novo duplications of the long arm of chromosome 9, including one case with Di George sequence.
Lindgren V; Rosinsky B; Chin J; Berry-Kravis E
Am J Med Genet; 1994 Jan; 49(1):67-73. PubMed ID: 8172253
[TBL] [Abstract][Full Text] [Related]
3. Use of fluorescence in situ hybridization to clarify a complex chromosomal rearrangement in a child with multiple congenital anomalies.
Spikes AS; Hegmann K; Smith JL; Shaffer LG
Am J Med Genet; 1995 May; 57(1):31-4. PubMed ID: 7645595
[TBL] [Abstract][Full Text] [Related]
4. Prenatal diagnosis of partial trisomy 1q using fluorescent in situ hybridization.
DuPont BR; Huff RW; Ridgway LE; Stratton RF; Moore CM
Am J Med Genet; 1994 Mar; 50(1):21-7. PubMed ID: 8160748
[TBL] [Abstract][Full Text] [Related]
5. [Fluorescence in situ hybridization in 6 patients with alterations of chromosome 18 and in 7 with marker chromosomes].
Esmer MC; Carnevale A; Gómez L; del Castillo V; Frías S
Rev Invest Clin; 1996; 48(1):27-33. PubMed ID: 8815483
[TBL] [Abstract][Full Text] [Related]
6. Partial duplication of the short arm of chromosome 2 (dup(2)(p13----p21) associated with mental retardation and an Aarskog-like phenotype.
Fryns JP; Kleczkowska A; Kenis H; Decock P; Van den Berghe H
Ann Genet; 1989; 32(3):174-6. PubMed ID: 2573314
[TBL] [Abstract][Full Text] [Related]
7. Diagnosis of four chromosome abnormalities of unknown origin by chromosome microdissection and subsequent reverse and forward painting.
Coêlho KE; Egashira M; Kato R; Fujimoto M; Matsumoto N; Rerkamnuaychoke B; Abe K; Harada N; Ohashi H; Fukushima Y; Niikawa N
Am J Med Genet; 1996 Jun; 63(3):468-71. PubMed ID: 8737654
[TBL] [Abstract][Full Text] [Related]
8. Interstitial duplication 19p.
Stratton RF; DuPont BR; Olsen AS; Fertitta A; Hoyer M; Moore CM
Am J Med Genet; 1995 Jul; 57(4):562-4. PubMed ID: 7573129
[TBL] [Abstract][Full Text] [Related]
9. Isochromosome-formation in chromosome 9.
Miller K; Arslan-Kirchner M
Ann Genet; 1994; 37(2):78-81. PubMed ID: 7985983
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. Cytogenetic and molecular analysis in trisomy 12p.
Allen TL; Brothman AR; Carey JC; Chance PF
Am J Med Genet; 1996 May; 63(1):250-6. PubMed ID: 8723118
[TBL] [Abstract][Full Text] [Related]
12. Confirmation of proximal 1q duplication using fluorescence in situ hybridization.
Chen H; Kusyk CJ; Tuck-Muller CM; Martinez JE; Dorand RD; Wertelecki W
Am J Med Genet; 1994 Mar; 50(1):28-31. PubMed ID: 8160749
[TBL] [Abstract][Full Text] [Related]
13. A distinct phenotype associated with partial trisomy 10q due to proximal direct duplication 10q11 --> q223?
van Buggenhout G; Decock P; Fryns JP
Genet Couns; 1996; 7(1):53-9. PubMed ID: 8652089
[TBL] [Abstract][Full Text] [Related]
14. Two sibs with different phenotypes due to adjacent-1 segregation of a subtle translocation t(4;5)(p16.3;p15.3)mat.
Qumsiyeh MB; Stevens CA
Am J Med Genet; 1993 Sep; 47(3):387-91. PubMed ID: 8135287
[TBL] [Abstract][Full Text] [Related]
15. Trisomy 20q caused by der(4) t(4;20) (q35;q13.1): report of a new patient and review of the literature.
Plotner PL; Smith JL; Northrup H
Am J Med Genet; 2002 Jul; 111(1):71-5. PubMed ID: 12124739
[TBL] [Abstract][Full Text] [Related]
16. Pericentric inversion with partial 7(q35-->qter) duplication and 7pter deletion: diagnosis by cytogenetic and fish analysis in a 29-year-old male patient.
Lukusa T; Van Buggenhout G; Devriendt K; Fryns JP
Genet Couns; 2002; 13(1):1-10. PubMed ID: 12017231
[TBL] [Abstract][Full Text] [Related]
17. Mild phenotype due to inverse duplication 4p16.3 - P15.3 including the Wolf-Hirschhorn critical region.
Tschernigg M; Petek E; Wagner K; Kroisel PM
Genet Couns; 2002; 13(1):29-33. PubMed ID: 12017235
[TBL] [Abstract][Full Text] [Related]
18. Characterization of a derivative chromosome 17 by fish-technique.
Ramesh KH; Shah HO; Sherman J; Lin JH; Verma RS
Ann Genet; 1996; 39(3):177-80. PubMed ID: 8839891
[TBL] [Abstract][Full Text] [Related]
19. Distal partial trisomy 1q: report of two cases and a review of the literature.
Utine GE; Aktas D; Alanay Y; Gücer S; Tuncbilek E; Mrasek K; Liehr T
Prenat Diagn; 2007 Sep; 27(9):865-71. PubMed ID: 17605151
[TBL] [Abstract][Full Text] [Related]
20. Delineation of a duplication map of chromosome 3q: a new case confirms the exclusion of 3q25-q26.2 from the duplication 3q syndrome critical region.
Rizzu P; Haddad BR; Vallcorba I; Alonso A; Ferro MT; Garcia-Sagredo JM; Baldini A
Am J Med Genet; 1997 Feb; 68(4):428-32. PubMed ID: 9021016
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]