273 related articles for article (PubMed ID: 18458513)
41. 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]
42. Prenatal diagnosis of a fetus with pure partial trisomy 1q32-44 due to a familial balanced rearrangement.
Kímya Y; Yakut T; Egelí U; Ozerkan K
Prenat Diagn; 2002 Nov; 22(11):957-61. PubMed ID: 12424755
[TBL] [Abstract][Full Text] [Related]
43. Partial trisomy 13q inherited from balanced translocation (5;13) (p14;q13).
Coco R; del Rey G
J Genet Hum; 1978 Dec; 26(4):303-10. PubMed ID: 752064
[TBL] [Abstract][Full Text] [Related]
44. 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]
45. Delineation of a supernumerary marker chromosome utilizing a multimodal approach of G-banding, fluorescent in situ hybridization, confirmatory P1 artificial chromosome fluorescent in situ hybridization, and high-resolution comparative genomic hybridization.
Mark HF; Wyandt H; Huang XL; Milunsky JM
Clin Genet; 2005 Aug; 68(2):146-51. PubMed ID: 15996211
[TBL] [Abstract][Full Text] [Related]
46. 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]
47. Partial 3q trisomy due to an unbalanced 3/10 translocation.
Blumberg B; Moore R; Mohandas T
Am J Med Genet; 1980; 7(3):335-9. PubMed ID: 7468658
[TBL] [Abstract][Full Text] [Related]
48. M-FISH applications in clinical genetics.
Cetin Z; Berker Karaüzüm S; Yakut S; Mihçi E; Baumer A; Wey E; Taçoy S; Bağci G; Lüleci G
Genet Couns; 2005; 16(3):257-68. PubMed ID: 16259323
[TBL] [Abstract][Full Text] [Related]
49. Distal 5q trisomy resulting from an X;5 translocation detected by chromosome painting.
Abuelo DN; Ahsanuddin AN; Mark HF
Am J Med Genet; 2000 Oct; 94(5):392-9. PubMed ID: 11050625
[TBL] [Abstract][Full Text] [Related]
50. A 21 years follow-up of a girl patient with a pseudodicentric bisatellited chromosome 22 associated with partial trisomy 22pter-->22q12.1: clinical, cytogenetic and molecular observations.
Vaglio A; Milunsky A; Huang XL; Quadrelli A; Mechoso B; Maher TA; Quadrelli R
Eur J Med Genet; 2008; 51(4):332-42. PubMed ID: 18316257
[TBL] [Abstract][Full Text] [Related]
51. Multiple congenital anomalies in association with supernumerary chromosome 47 inherited from a maternal balanced translocation.
Su PH; Chen JY; Hung HM; Chen JP; Wang CM; Chen SJ
J Formos Med Assoc; 2002 Apr; 101(4):301-3. PubMed ID: 12101870
[TBL] [Abstract][Full Text] [Related]
52. Interchange trisomy 9 due to maternal t(6;9) translocation.
Ninomiya S; Narahara K; Yokoyama Y; Tsuji K; Ito S; Akahori W; Akahori T; Seino Y
Acta Paediatr Jpn; 1994 Oct; 36(5):519-21. PubMed ID: 7825455
[TBL] [Abstract][Full Text] [Related]
53. Perinatal findings and molecular cytogenetic analysis of trisomy 16q and 22q13.3 deletion.
Chen CP; Lin SP; Chern SR; Shih SL; Lee CC; Wang W; Liao YW
Prenat Diagn; 2003 Jun; 23(6):504-8. PubMed ID: 12813767
[TBL] [Abstract][Full Text] [Related]
54. [Unbalanced subtelomic rearrangement involving 9q and 22q in a child with mental retardation and multiple congenital anomalies].
Xiao B; Xing Y; Ji X; Xu Y; Ni L; Zhu Y; Tao J
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2013 Dec; 30(6):666-9. PubMed ID: 24327143
[TBL] [Abstract][Full Text] [Related]
55. A malformed newborn with 9p and 4q trisomy.
Fryns JP; Azou M; Devliegher H; Eggermont E; van den Berghe H
Ann Genet; 1981; 24(1):48-50. PubMed ID: 6971619
[TBL] [Abstract][Full Text] [Related]
56. Maternal origin of extra marker chromosome 1Q31.1-qter and 13pter-q12.12 in a child with dysmorhic features.
Rao VB; Kerketta L; Korgaonkar S; Ghosh K; Mohanty D
Genet Couns; 2005; 16(2):139-43. PubMed ID: 16082769
[TBL] [Abstract][Full Text] [Related]
57. Newborn with malformations and a combined duplication of 9pter-q22 and 16q22-qter resulting from unbalanced segregation of a complex maternal translocation.
Piram A; Ortolan D; Peres LC; Pina-Neto JM; Riegel M; Schinzel A
Am J Med Genet A; 2003 Jul; 120A(2):247-52. PubMed ID: 12833408
[TBL] [Abstract][Full Text] [Related]
58. [Analysis of a pedigree with partial trisomy 9 and partial monosomy 13 derived from a maternal balanced t(9;13) translocation].
Sha Y; Mei L; Ji Z; Wang X; Lin S; Li L
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2019 Apr; 36(4):336-339. PubMed ID: 30950020
[TBL] [Abstract][Full Text] [Related]
59. Partial trisomy 1q41-qter and partial trisomy 9pter-9q21.32 in a newborn infant: an array CGH analysis and review.
Akalin I; Bozdag S; Spielmann M; Basaran SY; Nanda I; Klopocki E
Am J Med Genet A; 2014 Feb; 164A(2):490-4. PubMed ID: 24311106
[TBL] [Abstract][Full Text] [Related]
60. 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]
[Previous] [Next] [New Search]