BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

289 related articles for article (PubMed ID: 8160730)

  • 1. Two cases of Y; autosome translocations: A 45,X male and a clinically trisomy 18 patient.
    Farah SB; Ramos CF; de Mello MP; Sartorato EL; Horelli-Kuitunen N; Lopes VL; Cavalcanti DP; Hackel C
    Am J Med Genet; 1994 Feb; 49(4):388-92. PubMed ID: 8160730
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Pure partial trisomy 7q: two new patients and review.
    Rodríguez L; López F; Paisán L; de la Red Mdel M; Ruiz AM; Blanco M; Antelo Cortizas J; Martínez-Frías ML
    Am J Med Genet; 2002 Nov; 113(2):218-24. PubMed ID: 12407716
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A partial trisomy 15q due to 15;17 translocation detected by conventional cytogenetic and FISH techniques.
    Cora T; Acar H; Oran B
    Genet Couns; 2000; 11(1):25-32. PubMed ID: 10756424
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Identification of autosomal supernumerary chromosome markers (SMCs) by fluorescent in situ hybridization (FISH).
    Kolialexi A; Kitsiou S; Fryssira H; Sofocleous C; Kouvidi E; Tsangaris GT; Salavoura K; Mavrou A
    In Vivo; 2006; 20(4):473-8. PubMed ID: 16900777
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Fluorescene in situ hybridization establishes homology between human and silvered leaf monkey chromosomes, reveals reciprocal translocations between chromosomes homologous to human Y/5, 1/9, and 6/16, and delineates an X1X2Y1Y2/X1X1X2X2 sex-chromosome system.
    Bigoni F; Koehler U; Stanyon R; Ishida T; Wienberg J
    Am J Phys Anthropol; 1997 Mar; 102(3):315-27. PubMed ID: 9098501
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Identification of the origin of centromeres in whole-arm translocations using fluorescent in situ hybridization with alpha-satellite DNA probes.
    Tharapel AT; Qumsiyeh MB; Martens PR; Tharapel SA; Dalton JD; Ward JC; Wilroy RS
    Am J Med Genet; 1991 Jul; 40(1):117-20. PubMed ID: 1887840
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [2 new cases of Y-autosome translocation associated with azoospermia].
    Gregori-Romero M; López-Ginés C; Gil R; Galán Sánchez F; Pellín-Pérez A
    Rev Clin Esp; 1990 Jun; 187(2):71-3. PubMed ID: 2244061
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Unique (Y;13) translocation in a male with oligozoospermia: cytogenetic and molecular studies.
    Alves C; Carvalho F; Cremades N; Sousa M; Barros A
    Eur J Hum Genet; 2002 Aug; 10(8):467-74. PubMed ID: 12111641
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Trisomy 15 mosaicism owing to familial reciprocal translocation t(1;15): implication for prenatal diagnosis.
    Prontera P; Buldrini B; Aiello V; Gruppioni R; Bonfatti A; Venti G; Ferlini A; Sensi A; Calzolari E; Donti E
    Prenat Diagn; 2006 Jun; 26(6):571-6. PubMed ID: 16683276
    [TBL] [Abstract][Full Text] [Related]  

  • 10. An infertile male with balanced Y;19 translocation. Review of Y;autosome translocations.
    Smith A; Fraser IS; Elliott G
    Ann Genet; 1979; 22(4):189-194. PubMed ID: 399165
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Trisomy 18 and a constitutional maternal translocation (2;18).
    Teshima IE; Winsor EJ; Van Allen MI
    Am J Med Genet; 1992 Jul; 43(4):759-61. PubMed ID: 1621770
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Molecular studies of translocations and trisomy involving chromosome 13.
    Robinson WP; Bernasconi F; Dutly F; Lefort G; Romain DR; Binkert F; Schinzel AA
    Am J Med Genet; 1996 Jan; 61(2):158-63. PubMed ID: 8669444
    [TBL] [Abstract][Full Text] [Related]  

  • 13. E trisomy phenotype associated with small metacentric chromosome and a familial Y-22 translocation.
    Dumars KW; Fialko G; Larson E
    Birth Defects Orig Artic Ser; 1976; 12(5):97-104. PubMed ID: 953249
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Two cases with partial trisomy 9p: molecular cytogenetic characterization and clinical follow-up.
    Littooij AS; Hochstenbach R; Sinke RJ; van Tintelen P; Giltay JC
    Am J Med Genet; 2002 Apr; 109(2):125-32. PubMed ID: 11977161
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Trisomy of the distal 15q region due to familial balanced translocation t(15;16)(q24;p13) and unusual mosaicism in the mother of the proband].
    Nazarenko SA; Nazarenko LP; Baranova VA
    Tsitol Genet; 1987; 21(6):434-7. PubMed ID: 3445362
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Clinical and molecular cytogenetic studies in a case with partial trisomy 12p due to a de novo supernumerary ring chromosome.
    Ausems MG; Schuil J; Van Raveswaaij-Arts C; De Pater JM
    Genet Couns; 2004; 15(4):405-10. PubMed ID: 15658615
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Partial trisomy 13 due to maternal translocation t(7;13)(p22q14).
    Martin-Lucas MA; Pérez-Castillo A; Abrisqueta JA; de Torres ML; Martin-Sempere MJ; Del Mazo J; Aller V
    Ann Genet; 1982; 25(3):172-8. PubMed ID: 6982670
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Confirmation of trisomy 22 in two cases using chromosome painting: comparison with t(11;22).
    Slater HR; Voullaire LE; Vaux CE; Bankier A; Pertile M; Choo KH
    Am J Med Genet; 1993 Jun; 46(4):434-7. PubMed ID: 8357017
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Familial Y-autosome translocation in two unrelated girls.
    Funderburk SJ; Klisak I; Sparkes RS; Carrel RE
    Ann Genet; 1982; 25(2):119-22. PubMed ID: 6984628
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Cytogenetic and molecular genetic study on a female with complex translocation of t(Y;15) and t(14;21)].
    Shi Y; Ma S; Wang Y; Gao C; Ye L; Cheng Z
    Yi Chuan Xue Bao; 1993; 20(6):488-92. PubMed ID: 8179934
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 15.