127 related articles for article (PubMed ID: 1442891)
1. 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]
2. Detection of an unbalanced t(4;15) by FISH in a child with multiple congenital anomalies.
Celep F; Acar H; Aynaci O; Aynaci FM; Karagüzel A
Genet Couns; 2001; 12(4):319-26. PubMed ID: 11837600
[TBL] [Abstract][Full Text] [Related]
3. Jumping translocation in a newborn boy with dup(4q) and severe hydrops fetalis.
Duval E; van den Enden A; Vanhaesebrouck P; Speleman F
Am J Med Genet; 1994 Aug; 52(2):214-7. PubMed ID: 7802011
[TBL] [Abstract][Full Text] [Related]
4. Unbalanced translocation, t(18;21), detected by fluorescence in situ hybridization (FISH) in a child with 18q- syndrome and a ring chromosome 21.
McGinniss MJ; Rosenberg C; Stetten G; Schinzel AA; Binkert F; Petersen MB; Kearns WG; Kazazian HH; Pearson PL; Antonarakis SE
Am J Med Genet; 1993 Jul; 46(6):647-51. PubMed ID: 8362906
[TBL] [Abstract][Full Text] [Related]
5. 18q- and 18q+ mosaicism in a mentally retarded boy.
Ausems MG; Bhola SL; Post-Blok CA; Hennekam RC; de France HF
Am J Med Genet; 1994 Nov; 53(3):296-9. PubMed ID: 7856666
[TBL] [Abstract][Full Text] [Related]
6. Additional chromosome in a child as a result of a balanced reciprocal translocation t(12;18)(p13;q12) in his mother's karyotype.
Lassota M; Przełozna B; Płodzien M; Bugno M; Wnuk M; Kotylak Z; Słota E
J Appl Genet; 2005; 46(4):419-21. PubMed ID: 16278518
[TBL] [Abstract][Full Text] [Related]
7. 10p duplication characterized by fluorescence in situ hybridization.
Wiktor A; Feldman GL; Kratkoczki P; Ditmars DM; Van Dyke DL
Am J Med Genet; 1994 Sep; 52(3):315-8. PubMed ID: 7528972
[TBL] [Abstract][Full Text] [Related]
8. De novo translocation involving chromosomes 1 and 4 resulting in partial duplication of 4q and partial deletion of 1p.
Legare JM; Sekhon GS; Laxova R
Am J Med Genet; 1994 Nov; 53(3):216-21. PubMed ID: 7856655
[TBL] [Abstract][Full Text] [Related]
9. [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]
10. 15q duplication associated with autism in a multiplex family with a familial cryptic translocation t(14;15)(q11.2;q13.3) detected using array-CGH.
Koochek M; Harvard C; Hildebrand MJ; Van Allen M; Wingert H; Mickelson E; Holden JJ; Rajcan-Separovic E; Lewis ME
Clin Genet; 2006 Feb; 69(2):124-34. PubMed ID: 16433693
[TBL] [Abstract][Full Text] [Related]
11. Mosaicism with a normal cell line and an unbalanced structural rearrangement.
Zaslav AL; Fallet S; Blumenthal D; Jacob J; Fox J
Am J Med Genet; 1999 Jan; 82(1):15-9. PubMed ID: 9916836
[TBL] [Abstract][Full Text] [Related]
12. Mapping susceptibility gene locus for IgA deficiency at del(18)(q22.3-q23); report of familial cryptic chromosome t(18q; 10p) translocations.
Dostal A; Linnankivi T; Somer M; Kähkönen M; Litzman J; Tienari P
Int J Immunogenet; 2007 Jun; 34(3):143-7. PubMed ID: 17504501
[TBL] [Abstract][Full Text] [Related]
13. Molecular and clinical characterization of a recurrent cryptic unbalanced t(4q;18q) resulting in an 18q deletion and 4q duplication.
Horbinski C; Carter EM; Heard PL; Sathanoori M; Hu J; Vockley J; Gunn S; Hale DE; Surti U; Cody JD
Am J Med Genet A; 2008 Nov; 146A(22):2898-904. PubMed ID: 18932219
[TBL] [Abstract][Full Text] [Related]
14. Subtelomeric chromosomal rearrangements detected in patients with idiopathic mental retardation and dysmorphic features.
Caliskan MO; Karauzum SB; Mihci E; Tacoy S; Luleci G
Genet Couns; 2005; 16(2):129-38. PubMed ID: 16080292
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. A dysmorphic newborn infant with a complex rearrangement involving chromosomes 2, 4, and 6 detected by fluorescence in situ hybridization (FISH).
Hoffman DJ; Punnett HH; Pyeritz RE
Am J Perinatol; 2004 Feb; 21(2):69-71. PubMed ID: 15017469
[TBL] [Abstract][Full Text] [Related]
17. Duplication 20p identified via fluorescent in situ hybridization.
LeChien KA; McPherson E; Estop AM
Am J Med Genet; 1994 Apr; 50(2):187-9. PubMed ID: 7516625
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. Maternal balanced translocation leading to partial duplication of 4q and partial deletion of 1p in a son: cytogenetic and FISH studies using band-specific painting probes generated by chromosome microdissection.
Chen Z; Grebe TA; Guan XY; Notohamiprodjo M; Nutting PJ; Stone JF; Trent JM; Sandberg AA
Am J Med Genet; 1997 Aug; 71(2):160-6. PubMed ID: 9217215
[TBL] [Abstract][Full Text] [Related]
20. Presumptive monosomy 21 with neuronal migration disorder re-diagnosed as de novo unbalanced translocation t(18p;21q) by fluorescence in situ hybridisation.
Alkan M; Ramelli GP; Hirsiger H; Keser I; Remonda L; Bühler EM; Moser H
Genet Couns; 2002; 13(2):151-6. PubMed ID: 12150215
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
