BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

236 related articles for article (PubMed ID: 20461109)

  • 1. Genomic profile of copy number variants on the short arm of human chromosome 8.
    Yu S; Fiedler S; Stegner A; Graf WD
    Eur J Hum Genet; 2010 Oct; 18(10):1114-20. PubMed ID: 20461109
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Structural abnormalities of chromosome 8 and fetoplacental discrepancy: A second case report and review of fetal phenotype of 8p inverted duplication deletion syndrome.
    Huynh MT; Riteau AS; Moradkhani K; Pichon O; Richard S; Joubert M; Bézieau S
    Eur J Med Genet; 2021 Jan; 64(1):104118. PubMed ID: 33248287
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Fluorescence in situ hybridization and single nucleotide polymorphism of a new case with inv dup del(8p).
    Caglayan AO; Engelen JJ; Ghesquiere S; Alofs M; Saatci C; Dundar M
    Genet Couns; 2009; 20(4):333-40. PubMed ID: 20162868
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Telomere capture as a frequent mechanism for stabilization of the terminal chromosomal deletion associated with inverted duplication.
    Yu S; Graf WD
    Cytogenet Genome Res; 2010; 129(4):265-74. PubMed ID: 20606397
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Olfactory receptor-gene clusters, genomic-inversion polymorphisms, and common chromosome rearrangements.
    Giglio S; Broman KW; Matsumoto N; Calvari V; Gimelli G; Neumann T; Ohashi H; Voullaire L; Larizza D; Giorda R; Weber JL; Ledbetter DH; Zuffardi O
    Am J Hum Genet; 2001 Apr; 68(4):874-83. PubMed ID: 11231899
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Mild phenotype in a patient with mosaic del(8p)/inv dup del(8p).
    Hand M; Gray C; Glew G; Tsuchiya KD
    Am J Med Genet A; 2010 Nov; 152A(11):2827-31. PubMed ID: 20830805
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Inverted duplication deletion of 8P: characterization by standard cytogenetic and SNP array analyses.
    Sireteanu A; Braha E; Popescu R; Gramescu M; Gorduza EV; Rusu C
    Rev Med Chir Soc Med Nat Iasi; 2013; 117(3):731-4. PubMed ID: 24502041
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Postzygotic telomere capture causes segmental UPD, duplication and deletion of chromosome 8p in a patient with intellectual disability and obesity.
    Knijnenburg J; Uytdewilligen MEW; van Hassel DACM; Oostenbrink R; Eussen BHJ; de Klein A; Brooks AS; van Zutven LJCM
    Eur J Med Genet; 2017 Sep; 60(9):445-450. PubMed ID: 28602932
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Analysis of genomic copy number variations in two unrelated neonates with 8p deletion and duplication associated with congenital heart disease].
    Mei M; Yang L; Zhan G; Wang H; Ma D; Zhou W; Huang G
    Zhonghua Er Ke Za Zhi; 2014 Jun; 52(6):460-3. PubMed ID: 25190168
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Detection of a rare de novo 18p terminal deletion with inverted duplication in a Chinese pregnant woman.
    Zhu J; Qi H; Cao S; Cai L; Wen X; Tang G; Wan Q; Chen C; Wang J; Zeng W; Luo Y
    Mol Genet Genomic Med; 2019 Sep; 7(9):e868. PubMed ID: 31317671
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Independent post-zygotic breaks of a dicentric chromosome result in mosaicism for an inverted duplication deletion 9p and terminal deletion 9p.
    Schlade-Bartusiak K; Tucker T; Safavi H; Livingston J; van Allen MI; Eydoux P; Armstrong L
    Eur J Med Genet; 2013 May; 56(5):229-35. PubMed ID: 23416622
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Unusual 8p inverted duplication deletion with telomere capture from 8q.
    Buysse K; Antonacci F; Callewaert B; Loeys B; Fränkel U; Siu V; Mortier G; Speleman F; Menten B
    Eur J Med Genet; 2009; 52(1):31-6. PubMed ID: 19041960
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Dextrocardia, atrial septal defect, severe developmental delay, facial anomalies, and supernumerary ribs in a child with a complex unbalanced 8;22 translocation including partial 8p duplication.
    Pope K; Samanich J; Ramesh KH; Cannizzaro L; Pan Q; Babcock M
    Am J Med Genet A; 2012 Mar; 158A(3):641-7. PubMed ID: 22302699
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Clinical and cytogenetic findings in seven cases of inverted duplication of 8p with evidence of a telomeric deletion using fluorescence in situ hybridization.
    Guo WJ; Callif-Daley F; Zapata MC; Miller ME
    Am J Med Genet; 1995 Sep; 58(3):230-6. PubMed ID: 8533823
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Molecular characterization of inv dup del(8p): analysis of five cases.
    Shimokawa O; Kurosawa K; Ida T; Harada N; Kondoh T; Miyake N; Yoshiura K; Kishino T; Ohta T; Niikawa N; Matsumoto N
    Am J Med Genet A; 2004 Jul; 128A(2):133-7. PubMed ID: 15214003
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Clinical and molecular characterization of three genomic rearrangements at chromosome 22q13.3 associated with autism spectrum disorder.
    Chen CH; Chen HI; Liao HM; Chen YJ; Fang JS; Lee KF; Gau SS
    Psychiatr Genet; 2017 Feb; 27(1):23-33. PubMed ID: 27846046
    [TBL] [Abstract][Full Text] [Related]  

  • 17. The involvement of U-type dicentric chromosomes in the formation of terminal deletions with or without adjacent inverted duplications.
    Kato T; Inagaki H; Miyai S; Suzuki F; Naru Y; Shinkai Y; Kato A; Kanyama K; Mizuno S; Muramatsu Y; Yamamoto T; Shinya M; Tazaki Y; Hiwatashi S; Ikeda T; Ozaki M; Kurahashi H
    Hum Genet; 2020 Nov; 139(11):1417-1427. PubMed ID: 32488466
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Molecular cytogenetic characterization of inv dup del(8p) in a fetus associated with ventriculomegaly, hypoplastic left heart, polyhydramnios and intestinal obstruction.
    Chen CP; Ko TM; Huang WC; Chern SR; Wu PS; Chen YN; Chen SW; Lee CC; Pan CW; Yang CW; Wang W
    Taiwan J Obstet Gynecol; 2016 Jun; 55(3):415-8. PubMed ID: 27343326
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Molecular cytogenetic characterization of the first reported case of inv dup del 20p compatible with a U-type exchange model.
    Leclercq S; Maincent K; Baverel F; Tessier DL; Letourneur F; Lebbar A; Dupont JM
    Am J Med Genet A; 2009 Mar; 149A(3):437-45. PubMed ID: 19206177
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Analysis of invdupdel(8p) rearrangement: Clinical, cytogenetic and molecular characterization.
    García-Santiago FA; Martínez-Glez V; Santos F; García-Miñaur S; Mansilla E; Meneses AG; Rosell J; Granero ÁP; Vallespín E; Fernández L; Sierra B; Oliver-Bonet M; Palomares M; de Torres ML; Mori MÁ; Nevado J; Heath KE; Delicado A; Lapunzina P
    Am J Med Genet A; 2015 May; 167A(5):1018-25. PubMed ID: 25712135
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 12.