BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

141 related articles for article (PubMed ID: 2455825)

  • 21. Interstitial deletion of chromosome 1 (q23-q25). Report of a case.
    Silengo MC; Davi GF; Bianco R; Biagioli M; Guala A; Franceschini P; Novelli G
    Clin Genet; 1984 Jun; 25(6):549-52. PubMed ID: 6587954
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Three cases of 16q duplication.
    Maher ER; Willatt L; Cuthbert G; Chapman C; Hodgson SV
    J Med Genet; 1991 Nov; 28(11):801-2. PubMed ID: 1820771
    [No Abstract]   [Full Text] [Related]  

  • 23. 13S+. Giant satellites or de novo rearrangement?
    Imaizumi K; Kajii T; Niikawa N
    Hum Genet; 1981; 59(3):266-8. PubMed ID: 7327588
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Tandem duplication (1) (q11----q22) in a male infant with multiple congenital malformations.
    Mertens F; Johansson B; Forslund M; Olsson M; Kristoffersson U
    Clin Genet; 1987 Jul; 32(1):46-8. PubMed ID: 3621653
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Chromosomal abnormality (46,XX,3p plus) in a case of the Meckel syndrome.
    Hsia YE; Appadorai V; Breg WR; Howard RO
    Birth Defects Orig Artic Ser; 1974; 10(8):19-25. PubMed ID: 4142400
    [No Abstract]   [Full Text] [Related]  

  • 26. Analysis of banding patterns in a case of ring chromosome 21.
    Richer CL; Fitch N; Sitahal S; Murer-Orlando M; Jean P
    Am J Med Genet; 1981; 10(4):323-31. PubMed ID: 7332027
    [No Abstract]   [Full Text] [Related]  

  • 27. Ring chromosome 18 in a patient with multiple anomalies.
    Palmer CG; Fareed N; Merritt AD
    J Med Genet; 1967 Jun; 4(2):117-23. PubMed ID: 5619991
    [No Abstract]   [Full Text] [Related]  

  • 28. Partial trisomy of the short arm of chromosome 18 due to inversion duplication and direct duplication.
    Moog U; Engelen JJ; de Die-Smulders CE; Albrechts JC; Loneus WH; Haagen AA; Raven EJ; Hamers AJ
    Clin Genet; 1994 Dec; 46(6):423-9. PubMed ID: 7889659
    [TBL] [Abstract][Full Text] [Related]  

  • 29. [Ring chromosome 9].
    Kontiokari T; Borgström GH; Ritanen-Mohammed UM
    Duodecim; 1995; 111(5):439-41. PubMed ID: 8674446
    [No Abstract]   [Full Text] [Related]  

  • 30. Bilateral split hand and split foot malformation in a boy with a de novo interstitial deletion of 7q21.3.
    Roberts SH; Hughes HE; Davies SJ; Meredith AL
    J Med Genet; 1991 Jul; 28(7):479-81. PubMed ID: 1895319
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Ring chromosome 7 in a man with multiple congenital anomalies and mental retardation.
    Koiffmann CP; Diament A; de Souza DH; Wajntal A
    J Med Genet; 1990 Jul; 27(7):462-4. PubMed ID: 2395166
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Ring chromosome 14 in a mentally retarded girl.
    Iselius L; Ritzén M; Bui TH; Olsson K; Eklöf O
    Acta Paediatr Scand; 1980 Nov; 69(6):803-6. PubMed ID: 7211367
    [TBL] [Abstract][Full Text] [Related]  

  • 33. A ring chromosome, diagnosed by quinacrine fluorescence as No. 9, in a mentally retarded girl.
    Jacobsen P; Mikkelsen M; Rosleff F
    Clin Genet; 1973; 4(5):434-41. PubMed ID: 4127395
    [No Abstract]   [Full Text] [Related]  

  • 34. Identification of chromosomal abnormalities by quinacrine-staining technique in patients with normal karyotypes by conventional analysis.
    del Solar C; Uchida IA
    J Pediatr; 1974 Apr; 84(4):534-8. PubMed ID: 4134885
    [No Abstract]   [Full Text] [Related]  

  • 35. Identification of 21r and 22r chromosomes by quinacrine fluorescence.
    Crandall BF; Weber F; Muller HM; Burwell JK
    Clin Genet; 1972; 3(4):264-70. PubMed ID: 5054320
    [No Abstract]   [Full Text] [Related]  

  • 36. Duplication of distal 22q.
    Abeliovich D; Maor E; Bashan N; Carmi R
    Am J Med Genet; 1989 Mar; 32(3):346-9. PubMed ID: 2729354
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Pseudodicentric chromosome 18 diagnosed by chromosome painting and primed in situ labelling (PRINS).
    Brandt CA; Djernes B; Strømkjaer H; Petersen MB; Pedersen S; Hindkjaer J; Brinch-Iversen J; Bruun-Petersen G
    J Med Genet; 1994 Feb; 31(2):99-102. PubMed ID: 8182728
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Ring chromosome 8 in a boy with multiple congenital abnormalities and mental retardation.
    Hamers AJ; van Kempen C
    J Med Genet; 1977 Dec; 14(6):451-5. PubMed ID: 604497
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Ring chromosome 14: a distinct clinical entity.
    Schmidt R; Eviatar L; Nitowsky HM; Wong M; Miranda S
    J Med Genet; 1981 Aug; 18(4):304-7. PubMed ID: 7277427
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Case report. Familial 4-22 translocation with partial trisomy for the short arm of chromosome 4 in two sibs.
    Sartori A; Tenconi R; Baccichetti C; Pujatti G
    Acta Paediatr Scand; 1974 Jul; 63(4):631-5. PubMed ID: 4850900
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.