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 *

292 related articles for article (PubMed ID: 2077349)

  • 21. Transmission of ring 14 chromosome from mother to two sons.
    Matalon R; Supple P; Wyandt H; Rosenthal IM
    Am J Med Genet; 1990 Aug; 36(4):381-5. PubMed ID: 2202211
    [TBL] [Abstract][Full Text] [Related]  

  • 22. [Ring chromosome 17 and recurring pneumopathy].
    Lambruschini Ferri N; Ortola Castells ME; Rosell Andreo J; Ballesta Martínez F
    An Esp Pediatr; 1989 Nov; 31(5):478-80. PubMed ID: 2694873
    [No Abstract]   [Full Text] [Related]  

  • 23. Smallest critical region for microcephaly in a patient with mosaic ring chromosome 13.
    Su PH; Chen CP; Su YN; Chen SJ; Lin LL; Chen JY
    Genet Mol Res; 2013 Apr; 12(2):1311-7. PubMed ID: 23661454
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Use of chromosome painting for marker chromosome identification in two children with congenital disorders.
    Doco-Fenzy M; Navrocki B; Cornillet P; Sabouraud P; Robillard P; Gruson N; Gaillard D; Adnet JJ
    Bull Assoc Anat (Nancy); 1994 Jun; 78(241):9-13. PubMed ID: 8086666
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Prenatal diagnosis of de novo unbalanced translocation 8p;21q using subtelomeric probes.
    Ozkinay F; Kanit H; Onay H; Cogulu O; Gunduz C; Ercal D; Ozkinay C
    Genet Couns; 2006; 17(3):315-20. PubMed ID: 17100200
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Molecular analysis of a complex chromosomal rearrangement and a review of familial cases.
    Batista DA; Pai GS; Stetten G
    Am J Med Genet; 1994 Nov; 53(3):255-63. PubMed ID: 7856662
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Fetal anomalies associated with an inversion duplication 13 chromosome.
    Rijhsinghani AG; Hruban RH; Stetten G
    Obstet Gynecol; 1988 Jun; 71(6 Pt 2):991-4. PubMed ID: 3287254
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Trisomy 18 associated with a familial translocation t(Bq-; 18q+).
    France NE; Butler LJ
    Ann Genet; 1969 Mar; 12(1):46-50. PubMed ID: 5306711
    [No Abstract]   [Full Text] [Related]  

  • 29. Spectral karyotyping analysis of head and neck squamous cell carcinoma.
    Singh B; Gogineni S; Goberdhan A; Sacks P; Shaha A; Shah J; Rao P
    Laryngoscope; 2001 Sep; 111(9):1545-50. PubMed ID: 11568603
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Cytogenetics of fetal wastage.
    Kim HJ; Hsu LY; Paciuc S; Cristian S; Quintana A; Hirschhorn K
    N Engl J Med; 1975 Oct; 293(17):844-7. PubMed ID: 1177974
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Identification, counselling, and outcome of two cases of prenatally diagnosed supernumerary small ring chromosomes.
    Michalski K; Rauer M; Williamson N; Perszyk A; Hoo JJ
    Am J Med Genet; 1993 Apr; 46(1):88-94. PubMed ID: 8494036
    [TBL] [Abstract][Full Text] [Related]  

  • 32. 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]  

  • 33. A complex chromosome rearrangement with at least five breakpoints studied by fluorescence in situ hybridization.
    Gibson LH; McGrath J; Yang-Feng TL
    Am J Med Genet; 1997 Feb; 68(4):417-20. PubMed ID: 9021014
    [TBL] [Abstract][Full Text] [Related]  

  • 34. [Familial translocation t(4;22) (p11;p12) and trisomy 4p in 2 sisters].
    Giovannelli G; Forabosco A; Dutrillaux B
    Ann Genet; 1974 Jun; 17(2):119-24. PubMed ID: 4547939
    [No Abstract]   [Full Text] [Related]  

  • 35. A paternal balanced translocation [t(7;22)(q32;q13.3)] leading to reciprocal unbalanced karyotypes in two consecutive pregnancies.
    Zackowski JL; Raffel LJ; McDaniel LD; Schwartz S
    Ann Genet; 1990; 33(2):113-6. PubMed ID: 2241085
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Infertility and chromosome abnormality.
    Chandley AC
    Oxf Rev Reprod Biol; 1984; 6():1-46. PubMed ID: 6397710
    [No Abstract]   [Full Text] [Related]  

  • 37. Mosaic supernumerary r(8) syndrome.
    Yilmaz S; Tarkan-Argüden Y; Kuru D; Deviren A; Karaman B; Yüksel A; Hacihanefioğlu S
    Genet Couns; 2005; 16(2):187-90. PubMed ID: 16080301
    [No Abstract]   [Full Text] [Related]  

  • 38. Ring chromosome 13: lack of distinct syndromes based on different breakpoints on 13q.
    Brandt CA; Hertz JM; Petersen MB; Vogel F; Noer H; Mikkelsen M
    J Med Genet; 1992 Oct; 29(10):704-8. PubMed ID: 1433229
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Robertsonian (15q;15q) translocation in a child with Angelman syndrome: evidence of uniparental disomy.
    Tonk V; Schultz RA; Christian SL; Kubota T; Ledbetter DH; Wilson GN
    Am J Med Genet; 1996 Dec; 66(4):426-8. PubMed ID: 8989460
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Mitomycin C effect on Robertsonian translocations.
    Frias S; Carnevale A; Zavaleta MJ; Molina B
    Ann Genet; 1988; 31(3):162-6. PubMed ID: 3146941
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 15.