BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

202 related articles for article (PubMed ID: 25428228)

  • 1. Involvement of interstitial telomeric sequences in two new cases of mosaicism for autosomal structural rearrangements.
    Lévy J; Receveur A; Jedraszak G; Chantot-Bastaraud S; Renaldo F; Gondry J; Andrieux J; Copin H; Siffroi JP; Portnoï MF
    Am J Med Genet A; 2015 Feb; 167A(2):428-33. PubMed ID: 25428228
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. Molecular characterisation of a mosaicism with a complex chromosome rearrangement: evidence for coincident chromosome healing by telomere capture and neo-telomere formation.
    Chabchoub E; Rodríguez L; Galán E; Mansilla E; Martínez-Fernandez ML; Martínez-Frías ML; Fryns JP; Vermeesch JR
    J Med Genet; 2007 Apr; 44(4):250-6. PubMed ID: 17172463
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Prenatal Diagnosis of Trisomy 2p due to Terminal 2p Duplication including Interstitial Telomeric Sequences.
    Marlet L; Alix E; Till M; Raskin-Champion F; Attia J; Boggio D; Sanlaville D; Schluth-Bolard C
    Cytogenet Genome Res; 2017; 153(3):117-124. PubMed ID: 29268249
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Frequency of chromosome healing and interstitial telomeres in 40 cases of constitutional abnormalities.
    Fortin F; Beaulieu Bergeron M; Fetni R; Lemieux N
    Cytogenet Genome Res; 2009; 125(3):176-85. PubMed ID: 19738378
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Recurring germline mosaicism in a family due to reversion of an inherited derivative chromosome 8 from an 8;21 translocation with interstitial telomeric sequences.
    Bi W; Yuan B; Liu P; Murry JB; Qin X; Xia F; Quach T; Cooper LM; Wiszniewska J; Hixson P; Peacock S; Tonk VS; Huff RW; Ortega V; Lupski JR; Scherer SE; Littlejohn RO; Velagaleti GVN; Roeder ER; Cheung SW
    J Med Genet; 2023 Jun; 60(6):547-556. PubMed ID: 36150828
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. Submicroscopic terminal deletion of 1p36.3 and Xp23 hidden in complex chromosome rearrangements: independent mechanism of telomere restitution on the two chromatids.
    Reddy KS; Yang X
    Am J Med Genet A; 2003 Mar; 117A(3):261-7. PubMed ID: 12599190
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Association of structural and numerical anomalies of chromosome 22 in a patient with syndromic intellectual disability.
    Naoufal R; Legendre M; Couet D; Gilbert-Dussardier B; Kitzis A; Bilan F; Harbuz R
    Eur J Med Genet; 2016 Sep; 59(9):483-7. PubMed ID: 27452446
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Unbalanced cryptic 5p deletion/17p duplication identified by subtelomeric FISH in a family with a boy with chimerism and a balanced t(4;5).
    Ensenauer R; Jalal S; Meyer R; Babovic-Vuksanovic D
    Am J Med Genet A; 2004 Feb; 125A(1):86-91. PubMed ID: 14755472
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Detection of mutually exclusive mosaicism in a girl with genotype-phenotype discrepancies.
    Luo M; Mulchandani S; Dubbs HA; Swarr D; Pyle L; Zackai EH; Spinner NB; Conlin LK
    Am J Med Genet A; 2015 Dec; 167A(12):3091-5. PubMed ID: 26198585
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Three new cases with a mosaicism involving a normal cell line and a cryptic unbalanced autosomal reciprocal translocation.
    Gijsbers AC; Dauwerse JG; Bosch CA; Boon EM; van den Ende W; Kant SG; Hansson KM; Breuning MH; Bakker E; Ruivenkamp CA
    Eur J Med Genet; 2011; 54(4):e409-12. PubMed ID: 21664500
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Characterization of a Rare Mosaicism in Autosomal Translocation of t(5;21) Using Conventional Cytogenetics and FISH Methods.
    Omori Sarabi S; Karimzad Hagh J; Behrend C; Mohseni SB; Ansari Dezfouli M; Rashidi SK; Omrani MD
    Iran Biomed J; 2020 Jan; 24(1):60-3. PubMed ID: 31301695
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. Prenatal diagnosis of a fetus with pure partial trisomy 1q32-44 due to a familial balanced rearrangement.
    Kímya Y; Yakut T; Egelí U; Ozerkan K
    Prenat Diagn; 2002 Nov; 22(11):957-61. PubMed ID: 12424755
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Interstitial telomeric sequences at the junction site of a jumping translocation.
    Vermeesch JR; Petit P; Speleman F; Devriendt K; Fryns JP; Marynen P
    Hum Genet; 1997 Jun; 99(6):735-7. PubMed ID: 9187665
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. Prenatal detection of a subtle unbalanced chromosome rearrangement by karyotyping, FISH and array comparative genomic hybridization.
    Cain CC; Saul DO; Oehler E; Blakemore K; Stetten G
    Fetal Diagn Ther; 2008; 24(3):286-90. PubMed ID: 18818501
    [TBL] [Abstract][Full Text] [Related]  

  • 19. The presence of interstitial telomeric sequences in constitutional chromosome abnormalities.
    Park VM; Gustashaw KM; Wathen TM
    Am J Hum Genet; 1992 May; 50(5):914-23. PubMed ID: 1570843
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A Case of Trisomy 13 Mosaicism Presenting with a Severe Aortic Root Dilatation and Marfanoid Habitus due to an Unpredictable Cytogenetic Mechanism.
    Monin P; Reynaud N; Hanna N; Dupuis-Girod S; Till M; Arnaud P; Labalme A; Alix E; Poizat-Amar C; Faoucher M; Ravella L; Debost B; Obadia JF; Zech JC; Boileau C; Sanlaville D; Edery P; Putoux A; Schluth-Bolard C
    Cytogenet Genome Res; 2020; 160(2):72-79. PubMed ID: 32187601
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.