These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

137 related articles for article (PubMed ID: 12920085)

  • 21. A case of ring (9)/del(9p) mosaicism associated with gastroesophageal reflux.
    Leung AK; Rudd NL
    Am J Med Genet; 1988 Jan; 29(1):43-8. PubMed ID: 3344775
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Direct duplication of 8p21.3-->p23.1: a cytogenetic anomaly associated with developmental delay without consistent clinical features.
    Fan YS; Siu VM; Jung JH; Farrell SA; Côté GB
    Am J Med Genet; 2001 Oct; 103(3):231-4. PubMed ID: 11745996
    [TBL] [Abstract][Full Text] [Related]  

  • 23. dup(8p)/del(8q) recombinant chromosome in a girl with hepatic focal nodular hyperplasia.
    Tokutomi T; Hayashi S; Imai K; Chida A; Ishiwata T; Asano Y; Inazawa J; Nonoyama S
    Am J Med Genet A; 2007 Jun; 143A(12):1334-7. PubMed ID: 17506094
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Duplication 8 [inv dup(8)(p12p23)] with macrocephaly.
    Tonk VS; Wilson GN; Velagaleti GV
    Ann Genet; 2001; 44(4):195-9. PubMed ID: 11755105
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Mosaic tetrasomy 8p in two patients: clinical data and review of the literature.
    Schrander-Stumpel CT; Govaerts LC; Engelen JJ; van der Blij-Philipsen M; Borghgraef M; Loots WJ; Peters JJ; Rijnvos WP; Smeets DF; Fryns JP
    Am J Med Genet; 1994 May; 50(4):377-80. PubMed ID: 7516121
    [TBL] [Abstract][Full Text] [Related]  

  • 26. 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]  

  • 27. 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]  

  • 28. 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]  

  • 29. Inverted tandem duplication generates a duplication deficiency of chromosome 8p.
    Dill FJ; Schertzer M; Sandercock J; Tischler B; Wood S
    Clin Genet; 1987 Aug; 32(2):109-13. PubMed ID: 2888552
    [TBL] [Abstract][Full Text] [Related]  

  • 30. A case with de novo inv dup del(8p) associated with dextrocardia and corpus callosum agenesis.
    Ergün MA; Kula S; Karaer K; Perçin EF
    Pediatr Int; 2010 Oct; 52(5):845-6. PubMed ID: 20880309
    [No Abstract]   [Full Text] [Related]  

  • 31. Mosaic paternally derived inv dup(15) may partially rescue the Prader-Willi syndrome phenotype with uniparental disomy.
    Saitoh S; Hosoki K; Takano K; Tonoki H
    Clin Genet; 2007 Oct; 72(4):378-80. PubMed ID: 17850637
    [No Abstract]   [Full Text] [Related]  

  • 32. Inversion polymorphisms and non-contiguous terminal deletions: the cause and the (unpredicted) effect of our genome architecture.
    Ciccone R; Mattina T; Giorda R; Bonaglia MC; Rocchi M; Pramparo T; Zuffardi O
    J Med Genet; 2006 May; 43(5):e19. PubMed ID: 16648372
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Inverted duplications deletions: underdiagnosed rearrangements??
    Zuffardi O; Bonaglia M; Ciccone R; Giorda R
    Clin Genet; 2009 Jun; 75(6):505-13. PubMed ID: 19508415
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Chromosome duplications and deletions and their mechanisms of origin.
    Tharapel AT; Michaelis RC; Velagaleti GV; Laundon CH; Martens PR; Buchanan PD; Teague KE; Tharapel SA; Wilroy RS
    Cytogenet Cell Genet; 1999; 85(3-4):285-90. PubMed ID: 10449919
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Partial duplication 8p due to interstitial duplication: inv dup(8)(p21.1----p22). Further delineation of the phenotype from birth to adulthood.
    Kleczkowska A; Fryns JP; D'Hondt F; Jaeken J; Van den Berghe H
    Ann Genet; 1987; 30(1):47-51. PubMed ID: 3498429
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Stabilization of a terminal inversion duplication of 8p by telomere capture from 18q.
    Kostiner DR; Nguyen H; Cox VA; Cotter PD
    Cytogenet Genome Res; 2002; 98(1):9-12. PubMed ID: 12584435
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Another case of ring chromosome 9 associated with gastroesophageal reflux.
    Manouvrier-Hanu S; Turck D; Farriaux JP
    Am J Med Genet; 1989 Apr; 32(4):558. PubMed ID: 2774007
    [No Abstract]   [Full Text] [Related]  

  • 38. Mosaicism for duplication 12q (12q13-->12q21.2) accompanied by a pericentric inversion in a dysmorphic female infant.
    Vermeesch JR; Syrrou M; Salden I; Dhondt F; Matthijs G; Fryns JP
    J Med Genet; 2002 Nov; 39(11):e72. PubMed ID: 12414834
    [No Abstract]   [Full Text] [Related]  

  • 39. A Case Report of Respiratory Syncytial Virus-Infected 8p Inverted Duplication Deletion Syndrome with Low Natural Killer Cell Activity.
    Tokutake H; Chiba S
    Tohoku J Exp Med; 2022 Aug; 257(4):347-352. PubMed ID: 35768224
    [TBL] [Abstract][Full Text] [Related]  

  • 40. D8S7 is consistently deleted in inverted duplications of the short arm of chromosome 8 (inv dup 8p).
    Minelli A; Floridia G; Rossi E; Clementi M; Tenconi R; Camurri L; Bernardi F; Hoeller H; Previde Re C; Maraschio P
    Hum Genet; 1993 Oct; 92(4):391-6. PubMed ID: 7901142
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.