283 related articles for article (PubMed ID: 2495721)
1. De novo reciprocal 1p;2q translocation in a child with multiple congenital anomalies/mental retardation syndrome.
Chitayat D; Fagerstrom CL; Kalousek DK; Rootman J; Taylor GP; Hall JG
Am J Med Genet; 1989 Jan; 32(1):36-41. PubMed ID: 2495721
[TBL] [Abstract][Full Text] [Related]
2. Balanced complex chromosomal rearrangements with more than four breakpoints: report of a new case.
Till M; Devillard F; Crost P; Bachy M; Prieur F; Berthéas MF
Am J Med Genet; 1991 Sep; 40(3):370-3. PubMed ID: 1951445
[TBL] [Abstract][Full Text] [Related]
3. Rieger syndrome with de novo reciprocal translocation t(1;4) (q23.1;q25).
Makita Y; Masuno M; Imaizumi K; Yamashita S; Ohba S; Ito D; Kuroki Y
Am J Med Genet; 1995 May; 57(1):19-21. PubMed ID: 7645592
[TBL] [Abstract][Full Text] [Related]
4. Cohen syndrome and de novo reciprocal translocation t(5;7)(q33.1;p15.1).
Fryns JP; Kleczkowska A; Smeets E; Thiry P; Geutjens J; Van den Berghe H
Am J Med Genet; 1990 Dec; 37(4):546-7. PubMed ID: 2260606
[TBL] [Abstract][Full Text] [Related]
5. Interstitial deletion 1p as a result of a de novo reciprocal 1p;2p translocation.
Hertz JM; Jensen PH
Ann Genet; 1985; 28(4):228-30. PubMed ID: 3879434
[TBL] [Abstract][Full Text] [Related]
6. Toriello-Carey syndrome in a patient with a de novo balanced translocation [46,XY,t(2;14)(q33;q22)] interrupting SATB2.
Tegay DH; Chan KK; Leung L; Wang C; Burkett S; Stone G; Stanyon R; Toriello HV; Hatchwell E
Clin Genet; 2009 Mar; 75(3):259-64. PubMed ID: 19170718
[TBL] [Abstract][Full Text] [Related]
7. Malformative syndrome with trigonocephaly, shallow orbits, ptosis, growth and mental retardation. De novo autosomal reciprocal t(9;13)(Q32;Q22) in a male patient.
Fryns JP; Hendrickx G
Ann Genet; 1996; 39(1):51-3. PubMed ID: 9297446
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. [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]
10. A child with multiple congenital anomalies and karyotype 46,XY,del(14)(q31q32.3): further delineation of chromosome 14 interstitial deletion syndrome.
Gorski JL; Uhlmann WR; Glover TW
Am J Med Genet; 1990 Dec; 37(4):471-4. PubMed ID: 2260590
[TBL] [Abstract][Full Text] [Related]
11. Cytogenetic findings in 200 children with mental retardation and multiple congenital anomalies of unknown cause.
Coco R; Penchaszadeh VB
Am J Med Genet; 1982 Jun; 12(2):155-73. PubMed ID: 7102722
[TBL] [Abstract][Full Text] [Related]
12. Monosomy 1p36.31-33-->pter due to a paternal reciprocal translocation: prognostic significance of FISH analysis.
Blennow E; Bui TH; Wallin A; Kogner P
Am J Med Genet; 1996 Oct; 65(1):60-7. PubMed ID: 8914743
[TBL] [Abstract][Full Text] [Related]
13. [De novo balanced translocation in a child with mental retardation and malformations].
Gallego M; Coco R
Medicina (B Aires); 1981; 41(1):6-10. PubMed ID: 7266357
[No Abstract] [Full Text] [Related]
14. Severe microphthalmia, diaphragmatic hernia and Fallot's tetralogy associated with a chromosome 1;15 translocation.
Smith SA; Martin KE; Dodd KL; Young ID
Clin Dysmorphol; 1994 Oct; 3(4):287-91. PubMed ID: 7894732
[TBL] [Abstract][Full Text] [Related]
15. Autosomal dominant piebaldism and mental retardation syndrome associated with a t(1;2) (p22.1;q36).
Rivera H; Alvarez-Arratia MC; Moller M; Tinoco-Contreras M; Flores-Perez A; Cantu JM
J Genet Hum; 1986 Aug; 34(3-4):321-5. PubMed ID: 3760835
[TBL] [Abstract][Full Text] [Related]
16. A case of de novo trisomy 12p syndrome.
Ray M; Chudley AE; Christie N; Seargeant L
Ann Genet; 1985; 28(4):235-8. PubMed ID: 3879436
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. Double chromosome anomaly: interstitial deletion 5q and reciprocal translocation (1;11)(p22;q21).
de Michelena MI; Villacorta J; Chávez J
Am J Med Genet; 1990 May; 36(1):29-32. PubMed ID: 2185634
[TBL] [Abstract][Full Text] [Related]
19. Smith-Lemli-Opitz syndrome in a female with a de novo, balanced translocation involving 7q32: probable disruption of an SLOS gene.
Wallace M; Zori RT; Alley T; Whidden E; Gray BA; Williams CA
Am J Med Genet; 1994 May; 50(4):368-74. PubMed ID: 8209918
[TBL] [Abstract][Full Text] [Related]
20. A specific syndrome due to deletion of the distal long arm of chromosome 1.
Meinecke P; Vögtel D
Am J Med Genet; 1987 Oct; 28(2):371-6. PubMed ID: 3322005
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
