124 related articles for article (PubMed ID: 1719815)
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. A partial trisomy 15q due to 15;17 translocation detected by conventional cytogenetic and FISH techniques.
Cora T; Acar H; Oran B
Genet Couns; 2000; 11(1):25-32. PubMed ID: 10756424
[TBL] [Abstract][Full Text] [Related]
23. Proximal trisomy 1q in a girl with developmental delay and minor anomalies.
Furforo L; Rittler M; Slavutsky IR
Am J Med Genet; 1996 Sep; 64(4):551-5. PubMed ID: 8870921
[TBL] [Abstract][Full Text] [Related]
24. Partial trisomy 4(q31qter) due to maternal 4;5 balanced translocation in a neonate.
Senses DA; Silan F; Uzun H; Alagöz D; Zafer C; Kocabay K; Karaüzüm SB; Cetin Z
Genet Couns; 2007; 18(2):163-70. PubMed ID: 17710868
[TBL] [Abstract][Full Text] [Related]
25. Duplication 9q34-->qter identified by chromosome painting.
Spinner NB; Lucas JN; Poggensee M; Jacquette M; Schneider A
Am J Med Genet; 1993 Mar; 45(5):609-13. PubMed ID: 8456834
[TBL] [Abstract][Full Text] [Related]
26. Deletion (14) (q24.3q32.1): evidence for a distinct clinical phenotype.
Karnitis SA; Burns K; Sudduth KW; Golden WL; Wilson WG
Am J Med Genet; 1992 Sep; 44(2):153-7. PubMed ID: 1280909
[TBL] [Abstract][Full Text] [Related]
27. 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]
28. Subtelomeric FISH uncovers trisomy 14q32: lessons for imprinted regions, cryptic rearrangements and variant acrocentric short arms.
Sutton VR; Coveler KJ; Lalani SR; Kashork CD; Shaffer LG
Am J Med Genet; 2002 Sep; 112(1):23-7. PubMed ID: 12239715
[TBL] [Abstract][Full Text] [Related]
29. [4p trisomy secondary to paternal translocation t(4p-;15q+)].
Saad A; Khelif M; Kharrat H; Bouzakoura C
Ann Pediatr (Paris); 1991 May; 38(5):350-4. PubMed ID: 1872531
[TBL] [Abstract][Full Text] [Related]
30. Parental origin of the extra chromosome in the cat eye syndrome: evidence from heteromorphism and in situ hybridization analysis.
Magenis RE; Sheehy RR; Brown MG; McDermid HE; White BN; Zonana J; Weleber R
Am J Med Genet; 1988 Jan; 29(1):9-19. PubMed ID: 3344779
[TBL] [Abstract][Full Text] [Related]
31. Duplication of 7p21.2-->pter due to maternal 7p;21q translocation: implications for critical segment assignment in the 7p duplication syndrome.
Cai T; Yu P; Tagle DA; Xia J
Am J Med Genet; 1999 Oct; 86(4):305-11. PubMed ID: 10494083
[TBL] [Abstract][Full Text] [Related]
32. M-banding characterization of a 16p11.2p13.1 tandem duplication in a child with autism, neurodevelopmental delay and dysmorphism.
Behjati F; Shafaghati Y; Firouzabadi SG; Kahrizi K; Bagherizadeh I; Najmabadi H; Bint S; Ogilvie C
Eur J Med Genet; 2008; 51(6):608-14. PubMed ID: 18674645
[TBL] [Abstract][Full Text] [Related]
33. [Molecular-cytogenetic identification of partial trisomy of a short arm of chromosome 8].
Zerova-Liubimova TE; Rigel M; Smul'skaia NA; Evseenkova EG; Gorovenko NG; Shintzel A
Tsitol Genet; 2004; 38(4):55-61. PubMed ID: 15715166
[TBL] [Abstract][Full Text] [Related]
34. Identification and molecular confirmation of a small chromosome 10q duplication [dir dup(10)(q24.2-->q24.3)] inherited from a mother mosaic for the abnormality.
Tonk V; Schneider NR; Delgado MR; Mao J; Schultz RA
Am J Med Genet; 1996 Jan; 61(1):16-20. PubMed ID: 8741911
[TBL] [Abstract][Full Text] [Related]
35. 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]
36. [The phenotype of the trisomy of the short arm of chromosome no. 4. (a new case with t (4p; 11q) (author's transl)].
Kessel E; Pfeiffer RA; Kosenow W
Klin Padiatr; 1976 May; 188(3):215-9. PubMed ID: 945417
[TBL] [Abstract][Full Text] [Related]
37. 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]
38. Unbalanced inherited complex chromosome rearrangement involving chromosome 8, 10, 11 and 16 in a patient with congenital malformations and delayed development.
Karmous-Benailly H; Giuliano F; Massol C; Bloch C; De Ricaud D; Lambert JC; Perelman S
Eur J Med Genet; 2006; 49(5):431-8. PubMed ID: 16497571
[TBL] [Abstract][Full Text] [Related]
39. Trisomy of chromosome 16p13.3 due to an unbalanced insertional translocation into chromosome 22p13.
de Ravel T; Aerssens P; Vermeesch JR; Fryns JP
Eur J Med Genet; 2005; 48(3):355-9. PubMed ID: 16179232
[TBL] [Abstract][Full Text] [Related]
40. Reciprocal translocation between the proximal regions of the long arms of chromosomes 13 and 15 resulting in unbalanced offspring: characterization by fluorescence in situ hybridization and DNA analysis.
Mangelschots K; Van Roy B; Speleman F; Van Roy N; Gheuens J; Beuten J; Buntinx I; Van Thienen MN; Willekens H; Dumon J
Hum Genet; 1992 Jun; 89(4):407-13. PubMed ID: 1352272
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]