181 related articles for article (PubMed ID: 18679767)
1. Case report of de novo dup(18p)/del(18q) and r(18) mosaicism.
Gereltzul E; Baba Y; Suda N; Shiga M; Inoue MS; Tsuji M; Shin I; Hirata Y; Ohyama K; Moriyama K
J Hum Genet; 2008; 53(10):941-946. PubMed ID: 18679767
[TBL] [Abstract][Full Text] [Related]
2. Clinical and molecular-cytogenetic studies in seven patients with ring chromosome 18.
Stankiewicz P; Brozek I; Hélias-Rodzewicz Z; Wierzba J; Pilch J; Bocian E; Balcerska A; Wozniak A; Kardaś I; Wirth J; Mazurczak T; Limon J
Am J Med Genet; 2001 Jul; 101(3):226-39. PubMed ID: 11424138
[TBL] [Abstract][Full Text] [Related]
3. Del(18p) shown to be a cryptic translocation using a multiprobe FISH assay for subtelomeric chromosome rearrangements.
Horsley SW; Knight SJ; Nixon J; Huson S; Fitchett M; Boone RA; Hilton-Jones D; Flint J; Kearney L
J Med Genet; 1998 Sep; 35(9):722-6. PubMed ID: 9733029
[TBL] [Abstract][Full Text] [Related]
4. Prenatal diagnosis of 18p deletion and isochromosome 18q mosaicism in a fetus with a cystic hygroma.
Vičić A; Hafner T; Wagner J; Stipoljev F
Coll Antropol; 2014 Sep; 38(3):1059-62. PubMed ID: 25420396
[TBL] [Abstract][Full Text] [Related]
5. Low-level complex mosaic with multiple cell lines affecting the 18q21.31q21.32 region in a patient with de novo 18q terminal deletion.
Bonaglia MC; Fichera M; Marelli S; Romaniello R; Zuffardi O
Eur J Med Genet; 2022 Nov; 65(11):104596. PubMed ID: 36064004
[TBL] [Abstract][Full Text] [Related]
6. Familial pericentric inversion of chromosome 18: behavioral abnormalities in patients heterozygous for either the dup(18p)/del(18q) or dup(18q)/del(18p) recombinant chromosome.
Vermeulen SJ; Speleman F; Vanransbeeck L; Verspeet J; Menten B; Verschraegen-Spae MR; Wilde PD; Messiaen L; Michaelis RC; Leroy JG
Eur J Hum Genet; 2005 Jan; 13(1):52-8. PubMed ID: 15470365
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. [Genetic analysis of a case with mosaicism complex structural aberration of chromosome 18].
Shao M; Yan Z; Zhu X; Yan L; Qiao J
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2024 Jan; 41(1):101-105. PubMed ID: 38171568
[TBL] [Abstract][Full Text] [Related]
9. Unusual chromosomal mosaicism in Wolf-Hirschhorn syndrome: del(4)(p16)/der(4)(qter-q31.3::pter-qter).
Syrrou M; Borghgraef M; Fryns JP
Am J Med Genet; 2001 Dec; 104(3):199-203. PubMed ID: 11754044
[TBL] [Abstract][Full Text] [Related]
10. Precise mapping of a de novo duplication 18(q21-->q22) utilizing cytogenetic, biochemical, and molecular techniques.
Wolff DJ; Schwartz MF; Cohen MM; Schwartz S
Am J Med Genet; 1993 Jun; 46(5):520-3. PubMed ID: 8322813
[TBL] [Abstract][Full Text] [Related]
11. Cytogenetic, Molecular, and Phenotypic Characterization of a Patient with de novo Derivative Chromosome 18 and Review of the Literature.
Gökpınar İli E; Altıner Ş; Karabulut HG
Cytogenet Genome Res; 2019; 159(2):74-80. PubMed ID: 31658462
[TBL] [Abstract][Full Text] [Related]
12. [Genotypic and phenotypic analysis of a patient with de novo partial monosomy 18p and partial trisomy 18q].
Xiao B; Ji X; Ye H; Liu Y; Cao Y; Sun Y; Wei W; Qiu W
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2019 May; 36(5):484-487. PubMed ID: 31030439
[TBL] [Abstract][Full Text] [Related]
13. Identification and characterization of a new type of asymmetrical dicentric chromosome derived from a single maternal chromosome 18.
Lin CC; Li YC; Liu PP; Hsieh LJ; Cheng YM; Teng RH; Shi SL; Tsai FJ
Cytogenet Genome Res; 2007; 119(3-4):291-6. PubMed ID: 18253044
[TBL] [Abstract][Full Text] [Related]
14. Human chromosome 2 rod/ring mosaicism: probable origin by prezygotic breakage and intrachromosomal exchange.
Wyandt HE; Kasprzak R; Lamb A; Willson K; Wilson WG; Kelly TE
Cytogenet Cell Genet; 1982; 33(3):222-31. PubMed ID: 6957282
[TBL] [Abstract][Full Text] [Related]
15. 46,XY del(18)(q21.3q22.2) with mosaicism of r(18) and a milder form of the 18q- syndrome.
Maaswinkel-Mooij PD; de Jong P; Beverstock GC
Clin Genet; 1993 Feb; 43(2):76-8. PubMed ID: 8448905
[TBL] [Abstract][Full Text] [Related]
16. Prenatal diagnosis and molecular cytogenetic characterization of partial dup(18q)/del(18p) due to a paternal pericentric inversion 18 in a fetus with multiple anomalies.
Lee MJ; Park SH; Shim SH; Moon MJ; Cha DH
Taiwan J Obstet Gynecol; 2019 May; 58(3):318-323. PubMed ID: 31122516
[TBL] [Abstract][Full Text] [Related]
17. Ring chromosome 18q and jumping translocation 18p in an adult male with hypergonadotrophic hypogonadism.
Zahed L; Oreibi G; Azar C; Salti I
Am J Med Genet A; 2004 Aug; 129A(1):25-8. PubMed ID: 15266611
[TBL] [Abstract][Full Text] [Related]
18. Inv dup del(10q): identification by fluorescence in situ hybridization and array comparative genomic hybridization in a fetus with two concurrent chromosomal rearrangements.
Chen CP; Chen M; Su YN; Huang JP; Ma GC; Chang SP; Chern SR; Chen YT; Su JW; Lee CC; Town DD; Wang W
Taiwan J Obstet Gynecol; 2012 Jun; 51(2):245-52. PubMed ID: 22795102
[TBL] [Abstract][Full Text] [Related]
19. Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from ring chromosome 2.
Chen CP; Chen M; Chern SR; Wu PS; Chang SP; Lee DJ; Chen YT; Chen LF; Su JW; Hwa-Ruey Hsieh A; Hwa-Jiun Hsieh A; Wang W
Taiwan J Obstet Gynecol; 2012 Sep; 51(3):411-7. PubMed ID: 23040927
[TBL] [Abstract][Full Text] [Related]
20. Breakpoint mapping in a case of mosaicism with partial monosomy 9p23 --> pter and partial trisomy 1q41 --> qter suggests neo-telomere formation in stabilizing the deleted chromosome.
Kulikowski LD; Christ LA; Nogueira SI; Brunoni D; Schwartz S; Melaragno MI
Am J Med Genet A; 2006 Jan; 140(1):82-7. PubMed ID: 16333825
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
