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 *

152 related articles for article (PubMed ID: 10449645)

  • 1. Small terminal deletion of 1p and duplication of 1q: cytogenetics, FISH studies, and clinical observations at newborn and at age 16 years.
    Fan YS; Jung J; Hamilton B
    Am J Med Genet; 1999 Sep; 86(2):118-23. PubMed ID: 10449645
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Inv dup del (1)(pter-->q44::q44-->q42:) with the classical phenotype of trisomy 1q42-qter.
    De Brasi D; Rossi E; Giglio S; D'Agostino A; Titomanlio L; Farina V; Andria G; Sebastio G
    Am J Med Genet; 2001 Nov; 104(2):127-30. PubMed ID: 11746042
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Acute lymphoblastic leukemia in a patient with constitutional chromosome 1pter-p36.31 duplication and 1q43-qter deletion.
    Khan S; Toews H; Wang JC; Arredondo J; Provias J; Göhring G; Barr RD
    J Pediatr Hematol Oncol; 2012 Apr; 34(3):217-21. PubMed ID: 22217494
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Maternal balanced translocation leading to partial duplication of 4q and partial deletion of 1p in a son: cytogenetic and FISH studies using band-specific painting probes generated by chromosome microdissection.
    Chen Z; Grebe TA; Guan XY; Notohamiprodjo M; Nutting PJ; Stone JF; Trent JM; Sandberg AA
    Am J Med Genet; 1997 Aug; 71(2):160-6. PubMed ID: 9217215
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Molecular cytogenetic characterization of a derivative chromosome 8 with an inverted duplication of 8p21.3-->p23.3 and a rearranged duplication of 8q24.13-->qter.
    Fan YS; Siu VM
    Am J Med Genet; 2001 Aug; 102(3):266-71. PubMed ID: 11484205
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A case of duplication of 13q32-->qter and deletion of 18p11.32-->pter with mild phenotype: Patau syndrome and duplications of 13q revisited.
    Helali N; Iafolla AK; Kahler SG; Qumsiyeh MB
    J Med Genet; 1996 Jul; 33(7):600-2. PubMed ID: 8818949
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. FISH and cytogenetic characterization of a terminal chromosome 1q deletion: clinical case report and phenotypic implications.
    Gentile M; Di Carlo A; Volpe P; Pansini A; Nanna P; Valenzano MC; Buonadonna AL
    Am J Med Genet A; 2003 Mar; 117A(3):251-4. PubMed ID: 12599188
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A dysmorphic newborn with 45,X,der(1)inv(1)(p13;qter)t(Y;1)(pter-->q11;p13),-Y de novo karyotype.
    Tatar A; Oztas S; Yakut T; Ors R
    Genet Couns; 2005; 16(2):173-7. PubMed ID: 16080298
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Duplication dup(1)(q32q44) detected by comparative genomic hybridization (CGH): further delineation of trisomies 1q.
    Bartsch C; Aslan M; Köhler J; Miny P; Horst J; Holzgreve W; Rehder H; Fritz B
    Fetal Diagn Ther; 2001; 16(5):265-73. PubMed ID: 11509847
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Detection of a de novo duplication of 1q32-qter by fluorescence in situ hybridisation in a boy with multiple malformations: further delineation of the trisomy 1q syndrome.
    Duba HC; Erdel M; Löffler J; Bereuther L; Fischer H; Utermann B; Utermann G
    J Med Genet; 1997 Apr; 34(4):309-13. PubMed ID: 9138155
    [TBL] [Abstract][Full Text] [Related]  

  • 12. De novo 1q32q44 duplication and distal 1q trisomy syndrome.
    Nowaczyk MJ; Bayani J; Freeman V; Watts J; Squire J; Xu J
    Am J Med Genet A; 2003 Jul; 120A(2):229-33. PubMed ID: 12833404
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Interstitial duplication of the short arm of chromosome 1 in a newborn with congenital heart disease and multiple malformations.
    Warden CR; Pillers DA; Rice MJ; Wildes J; Livingston JS; Clark BA; Gilhooly JT; Magenis RE
    Am J Med Genet; 2001 Jun; 101(2):100-5. PubMed ID: 11391651
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Chromosome 1p36 deletion syndrome: prenatal diagnosis, molecular cytogenetic characterization and fetal ultrasound findings.
    Chen CP; Chen M; Su YN; Hsu CY; Tsai FJ; Chern SR; Wu PC; Lee CC; Wang W
    Taiwan J Obstet Gynecol; 2010 Dec; 49(4):473-80. PubMed ID: 21199750
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Cryptic duplication and deletion of 9q34.3 --> qter in a family with a t(9;22)(q34.3;p11.2).
    Sanger TM; Olney AH; Zaleski D; Pickering D; Nelson M; Sanger WG; Dave BJ
    Am J Med Genet A; 2005 Sep; 138(1):51-5. PubMed ID: 16104013
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Translocation breakpoint mapping and sequence analysis in three monosomy 1p36 subjects with der(1)t(1;1)(p36;q44) suggest mechanisms for telomere capture in stabilizing de novo terminal rearrangements.
    Ballif BC; Wakui K; Gajecka M; Shaffer LG
    Hum Genet; 2004 Jan; 114(2):198-206. PubMed ID: 14579147
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Identification of de novo chromosome rearrangements: five cases analyzed with differential chromosome painting.
    Ida T; Harada N; Abe K; Kondoh T; Yoshinaga M; Maki T; Niikawa N
    Am J Med Genet; 2002 Mar; 108(3):182-6. PubMed ID: 11891682
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Comparative genomic hybridization reveals a partial de novo trisomy 6q23-qter in an infant with congenital malformations: delineation of the phenotype.
    Erdel M; Duba HC; Verdorfer I; Lingenhel A; Geiger R; Gutenberger KH; Ludescher E; Utermann B; Utermann G
    Hum Genet; 1997 May; 99(5):596-601. PubMed ID: 9150724
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Chromosome 18q-syndrome and 1p terminal duplication in a patient with bilateral vesico-ureteral reflux: case report and literature revision.
    Brandigi E; Molinaro F; Bulotta AL; Angotti R; Pavone M; Messina M
    Ital J Pediatr; 2013 Jan; 39():6. PubMed ID: 23343423
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Monosomy 1p36.31-33-->pter due to a paternal reciprocal translocation: prognostic significance of FISH analysis.
    Blennow E; Bui TH; Wallin A; Kogner P
    Am J Med Genet; 1996 Oct; 65(1):60-7. PubMed ID: 8914743
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.