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 *

104 related articles for article (PubMed ID: 8986272)

  • 21. [Cytogenetic and molecular genetic diagnostics of Rett syndrome in children].
    Vorsanova SG; Demidova IA; Ulas VIu; Solov'ev IV; Kravets VS; Kazantseva LZ; Iurov IuB
    Zh Nevrol Psikhiatr Im S S Korsakova; 1998; 98(4):53-6. PubMed ID: 9606901
    [TBL] [Abstract][Full Text] [Related]  

  • 22. A Philadelphia chromosome positive CML patient with a unique translocation studied via GTG-banding and fluorescence in situ hybridization.
    Young C; Di Benedetto J; Glasser L; Mark HF
    Cancer Genet Cytogenet; 1996 Jul; 89(2):157-62. PubMed ID: 8697424
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Oligo-based aCGH analysis reveals cryptic unbalanced der(6)t(X;6) in pediatric t(12;21)-positive acute lymphoblastic leukemia.
    Kjeldsen E
    Exp Mol Pathol; 2016 Aug; 101(1):38-43. PubMed ID: 27215399
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Duplication of 8p23.1: a cytogenetic anomaly with no established clinical significance.
    Barber JC; Joyce CA; Collinson MN; Nicholson JC; Willatt LR; Dyson HM; Bateman MS; Green AJ; Yates JR; Dennis NR
    J Med Genet; 1998 Jun; 35(6):491-6. PubMed ID: 9643291
    [TBL] [Abstract][Full Text] [Related]  

  • 25. [Familial pericentric inversion of the X chromosome [inv(X)(p11q28)]].
    Baumann W; Zabel B; Holl M
    Ann Genet; 1984; 27(2):106-8. PubMed ID: 6331785
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Applications of comparative genomic hybridisation in constitutional chromosome studies.
    Breen CJ; Barton L; Carey A; Dunlop A; Glancy M; Hall K; Hegarty AM; Khokhar MT; Power M; Ryan K; Green AJ; Stallings RL
    J Med Genet; 1999 Jul; 36(7):511-7. PubMed ID: 10424810
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Cytogenetics of the chronic myeloid leukemia-derived cell line K562: karyotype clarification by multicolor fluorescence in situ hybridization, comparative genomic hybridization, and locus-specific fluorescence in situ hybridization.
    Gribble SM; Roberts I; Grace C; Andrews KM; Green AR; Nacheva EP
    Cancer Genet Cytogenet; 2000 Apr; 118(1):1-8. PubMed ID: 10731582
    [TBL] [Abstract][Full Text] [Related]  

  • 28. A 45,X male with molecular evidence of a translocation of Y euchromatin onto chromosome 1.
    Abbas N; Novelli G; Stella NC; Triolo O; Corrado F; Fellous M; Chery M; Gilgenkrantz S; Dallapiccola B
    Hum Genet; 1990 Nov; 86(1):94-8. PubMed ID: 2253943
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Application of fluorescent in situ hybridization with X and Y chromosome specific probes to buccal smear analysis.
    Schad CR; Kuffel DG; Wyatt WA; Zinsmeister AR; Jenkins RB; Dewald GW; Jalal SM
    Am J Med Genet; 1996 Dec; 66(2):187-92. PubMed ID: 8958328
    [TBL] [Abstract][Full Text] [Related]  

  • 30. The penta-X syndrome.
    Monheit A; Francke U; Saunders B; Jones KL
    J Med Genet; 1980 Oct; 17(5):392-6. PubMed ID: 7218280
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Partial duplication of Xp: a case report and review of previously reported cases.
    Wyandt HE; Bugeau-Michaud L; Skare JC; Milunsky A
    Am J Med Genet; 1991 Sep; 40(3):280-3. PubMed ID: 1951429
    [TBL] [Abstract][Full Text] [Related]  

  • 32. DNA hybridization study using Y-specific probes in an XX-male.
    Fuse H; Satomi S; Kazama T; Katayama T; Nagabuchi S; Tamura T; Nakahori Y; Nakagome Y
    Andrologia; 1991; 23(3):237-9. PubMed ID: 1741489
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Opposite deletions/duplications of the X chromosome: two novel reciprocal rearrangements.
    Giglio S; Pirola B; Arrigo G; Dagrada P; Bardoni B; Bernardi F; Russo G; Argentiero L; Forabosco A; Carrozzo R; Zuffardi O
    Eur J Hum Genet; 2000 Jan; 8(1):63-70. PubMed ID: 10713889
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Maternal balanced translocation leading to partial duplication of 4q and partial deletion of 1p in a son: cytogenetic and FISH studies using band-specific painting probes generated by chromosome microdissection.
    Chen Z; Grebe TA; Guan XY; Notohamiprodjo M; Nutting PJ; Stone JF; Trent JM; Sandberg AA
    Am J Med Genet; 1997 Aug; 71(2):160-6. PubMed ID: 9217215
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Characterization of a highly complex region in Xq13 and mapping of three isodicentric breakpoints associated with preleukemia.
    McDonell N; Ramser J; Francis F; Vinet MC; Rider S; Sudbrak R; Riesselman L; Yaspo ML; Reinhardt R; Monaco AP; Ross F; Kahn A; Kearney L; Buckle V; Chelly J
    Genomics; 2000 Mar; 64(3):221-9. PubMed ID: 10756090
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Complete cytogenetic characterization of the human breast cancer cell line MA11 combining G-banding, comparative genomic hybridization, multicolor fluorescence in situ hybridization, RxFISH, and chromosome-specific painting.
    Micci F; Teixeira MR; Heim S
    Cancer Genet Cytogenet; 2001 Nov; 131(1):25-30. PubMed ID: 11734314
    [TBL] [Abstract][Full Text] [Related]  

  • 37. [Multiple FISH and multiple BAND: Application of cytogenetic and molecular techniques in 5 cases].
    Castillo Taucher S; Fuentes AM; Paulos A; Pardo A
    Rev Med Chil; 2002 May; 130(5):511-8. PubMed ID: 12143271
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Cytogenetics of three breeds of river buffalo (Bubalus bubalis L.), with evidence of a fragile site on the X chromosome.
    Pires RM; Reichert RH; Kasahara S
    Theriogenology; 1998 Feb; 49(3):529-38. PubMed ID: 10732032
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Molecular cytogenetic analysis of the monoblastic cell line U937. karyotype clarification by G-banding, whole chromosome painting, microdissection and reverse painting, and comparative genomic hybridization.
    Lee JY; Lee CH; Shim SH; Seo HK; Kyhm JH; Cho S; Cho YH
    Cancer Genet Cytogenet; 2002 Sep; 137(2):124-32. PubMed ID: 12393283
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Partial Xp duplication in a girl with dysmorphic features: the change in replication pattern of late-replicating dupX chromosome.
    Kokalj Vokac N; Seme Ciglenecki P; Erjavec A; Zagradisnik B; Zagorac A
    Clin Genet; 2002 Jan; 61(1):54-61. PubMed ID: 11903357
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 6.