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 *

147 related articles for article (PubMed ID: 11891691)

  • 1. Patient with rheumatoid arthritis and MCA/MR syndrome due to unbalanced der(18) transmission of a paternal translocation t(18;20)(p11.1;p11.1).
    Czakó M; Riegel M; Morava E; Schinzel A; Kosztolányi G
    Am J Med Genet; 2002 Mar; 108(3):226-8. PubMed ID: 11891691
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Mosaic rearrangement of chromosome 18: characterization by FISH mapping and DNA studies shows trisomy 18p and monosomy 18p both of paternal origin.
    Oner G; Jauch A; Eggermann T; Hardwick R; Kirsch S; Schiebel K; Rappold G; Robson L; Smith A
    Am J Med Genet; 2000 May; 92(2):101-6. PubMed ID: 10797432
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Prenatal diagnosis and characterization of an unbalanced whole arm translocation resulting in monosomy for 18p.
    McGhee EM; Qu Y; Wohlferd MM; Goldberg JD; Norton ME; Cotter PD
    Clin Genet; 2001 Apr; 59(4):274-8. PubMed ID: 11298684
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Cryptic unbalanced translocation t(17;18)(p13.2;q22.3) identified by subtelomeric FISH and defined by array-based comparative genomic hybridization in a patient with mental retardation and dysmorphic features.
    Hwang KS; Pearson MA; Stankiewicz P; Lennon PA; Cooper ML; Wu J; Ou Z; Cai WW; Patel A; Cheung SW
    Am J Med Genet A; 2005 Aug; 137(1):88-93. PubMed ID: 16015583
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. Detection of a cryptic translocation t(13;20)(q34;p13) in an unexplained case of MCA/MR: value of FISH over high resolution banding.
    de Die-Smulders CE; Engelen JJ; Albrechts JC; Hamers GJ
    Am J Med Genet; 1999 Oct; 86(4):385-8. PubMed ID: 10494096
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Prenatal diagnosis of a fetus with a cryptic translocation 4p;18p and Wolf-Hirschhorn syndrome (WHS).
    Kohlschmidt N; Zielinski J; Brude E; Schäfer D; Olert J; Hallermann C; Coerdt W; Arnemann J
    Prenat Diagn; 2000 Feb; 20(2):152-5. PubMed ID: 10694689
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Analysis of a whole arm translocation between chromosomes 18 and 20 using fluorescence in situ hybridization: detection of a break in the centromeric alpha-satellite sequences.
    Tümer Z; Berg A; Mikkelsen M
    Hum Genet; 1995 Mar; 95(3):299-302. PubMed ID: 7868122
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Paternal origin of der(X)t(X;6) in a girl with trisomy 6p and unbalanced t(6;10) mosaicism in her mother.
    Petković I; Barisić I; Bastić M; Hećimović S; Bago R
    Am J Med Genet A; 2003 Jul; 120A(2):266-71. PubMed ID: 12833412
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Partial trisomy of chromosome 18 (pter----q12) following a familial 18;21 translocation rcp(18;21)(q12;q11).
    Binkert F; Stranzinger J; Schinzel A
    Hum Hered; 1990; 40(2):81-4. PubMed ID: 2335369
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Fluorescence in situ hybridization (FISH) of a whole-arm translocation involving chromosomes 18 and 20 with alpha-satellite DNA probes: detection of a centromeric DNA break?
    Cantú ES; Khan TA; Pai GS
    Am J Med Genet; 1992 Oct; 44(3):340-4. PubMed ID: 1488982
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Lissencephaly with der(17)t(17;20)(p13.3;p12.2)mat.
    Thomas MA; Duncan AM; Bardin C; Kaloustian VM
    Am J Med Genet A; 2004 Jan; 124A(3):292-5. PubMed ID: 14708103
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A de novo subterminal trisomy 10p and monosomy 18q in a girl with MCA/MR: case report and review.
    Courtens W; Wuyts W; Scheers S; Van Luijk R; Reyniers E; Rooms L; Ceulemans B; Kooy F; Wauters J
    Eur J Med Genet; 2006; 49(5):402-13. PubMed ID: 16488200
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Segregation of a t(1;3) translocation in multiple affected family members with both types of adjacent-1 segregants.
    Kozma C; Slavotinek AM; Meck JM
    Am J Med Genet A; 2004 Jan; 124A(2):118-28. PubMed ID: 14699608
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Basilar artery dolichoectasia in a boy with a combination of partial monosomy 18p and partial trisomy 20q.
    Su PH; Chen JY; Chen SJ; Yang MS; Liu YL
    Clin Dysmorphol; 2006 Oct; 15(4):225-228. PubMed ID: 16957478
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Trisomy 17p due to a t(8;17) (p23;p11.2)pat translocation. Case report and review of the literature.
    Schrander-Stumpel C; Schrander J; Fryns JP; Hamers G
    Clin Genet; 1990 Feb; 37(2):148-52. PubMed ID: 2178819
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A father and son with mental retardation, a characteristic face, inv(12), and insertion trisomy 12p12.3-p11.2.
    Liang D; Wu L; Pan Q; Harada N; Long Z; Xia K; Yoshiura K; Dai H; Niikawa N; Cai F; Xia J
    Am J Med Genet A; 2006 Feb; 140(3):238-44. PubMed ID: 16411213
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A FEMALE PATIENT WITH DUPLICATION OF 7p13-pter ASSOCIATED WITH DEL 20p13pter RESULTING FROM MALSEGREGATED PATERNAL 7;20 BALANCED TRANSLOCATION.
    Eid MO; Eid MM; Kamel AK; El-Ruby M; Abdel-Salam GM
    Genet Couns; 2015; 26(2):153-61. PubMed ID: 26349184
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Optic disk and white matter abnormalities in a patient with a de novo 18p partial monosomy.
    Abu-Amero KK; Hellani A; Salih MA; Alorainy IA; Zidan G; Kern KC; Sicotte NL; Bosley TM
    Ophthalmic Genet; 2010 Sep; 31(3):147-54. PubMed ID: 20565246
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Subtelomeric deletion of 18p in an adult with paranoid schizophrenia and mental retardation.
    Babovic-Vuksanovic D; Jenkins SC; Ensenauer R; Newman DC; Jalal SM
    Am J Med Genet A; 2004 Jan; 124A(3):318-22. PubMed ID: 14708108
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.