BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

228 related articles for article (PubMed ID: 8641683)

  • 1. Interstitial deletion of chromosome 6q: precise definition of the breakpoints by microdissection, DNA amplification, and reverse painting.
    Rubtsov N; Senger G; Kuzcera H; Neumann A; Kelbova C; Junker K; Beensen V; Claussen U
    Hum Genet; 1996 Jun; 97(6):705-9. PubMed ID: 8641683
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Subtle overlapping deletions in the terminal region of chromosome 6q24.2-q26: three cases studied using FISH.
    Sukumar S; Wang S; Hoang K; Vanchiere CM; England K; Fick R; Pagon B; Reddy KS
    Am J Med Genet; 1999 Nov; 87(1):17-22. PubMed ID: 10528241
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Two patients with chromosome 6q terminal deletions with breakpoints at q24.3 and q25.3.
    Meng J; Fujita H; Nagahara N; Kashiwai A; Yoshioka Y; Funato M
    Am J Med Genet; 1992 Jul; 43(4):747-50. PubMed ID: 1621768
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A case of a female infant with simultaneous occurrence of de novo terminal deletions on chromosome 14q and 20p.
    Uehara S; Akai Y; Takeyama Y; Okamura K; Takabayashi T; Yajima A; Natsui M; Nakai H
    Clin Genet; 1993 Jan; 43(1):28-33. PubMed ID: 8179640
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Mosaic r(13) resulting in large deletion of chromosome 13q in a newborn female with multiple congenital anomalies.
    Lorentz CP; Jalal SM; Thompson DM; Babovic-Vuksanovic D
    Am J Med Genet; 2002 Jul; 111(1):61-7. PubMed ID: 12124737
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Characterization of an interstitial deletion del(13)(q22q32) using microdissection and sequential FISH and G-banding.
    Xu J; Chernos JE; Bernier F; Lowry RB
    Genet Test; 2000; 4(3):279-82. PubMed ID: 11142759
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Distal deletion, del(2)(q33.3q33.3), in a patient with severe growth deficiency and minor anomalies.
    Riegel M; Morava E; Czakó M; Kosztolányi G; Schinzel A
    Am J Med Genet; 2001 Aug; 102(3):227-30. PubMed ID: 11484198
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Interstitial deletion of 6q25.2-q25.3: a novel microdeletion syndrome associated with microcephaly, developmental delay, dysmorphic features and hearing loss.
    Nagamani SC; Erez A; Eng C; Ou Z; Chinault C; Workman L; Coldwell J; Stankiewicz P; Patel A; Lupski JR; Cheung SW
    Eur J Hum Genet; 2009 May; 17(5):573-81. PubMed ID: 19034313
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Proximal interstitial 6q deletion: a recognizable syndrome.
    Kumar R; Riordan D; Dawson AJ; Chudley AE
    Am J Med Genet; 1997 Aug; 71(3):353-6. PubMed ID: 9268108
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Specification of small distal 6q deletions in two patients by gene dosage and in situ hybridization study of plasminogen and alpha-L-fucosidase 2.
    Narahara K; Tsuji K; Yokoyama Y; Namba H; Murakami M; Matsubara T; Kasai R; Fukushima Y; Seki T; Wakui K
    Am J Med Genet; 1991 Sep; 40(3):348-53. PubMed ID: 1951444
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Partial trisomy 1q (1q42.13-->qter) and partial monosomy 6q (6q27-->qter) in a girl with single median maxillary central incisor, corpus callosum dysgenesis and developmental delay.
    Chen CP; Lin SP; Su YN; Chern SR; Su JW; Lee CC; Wang W
    Genet Couns; 2012; 23(4):447-55. PubMed ID: 23431743
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Molecular cytogenetic analysis of a constitutional de novo interstitial deletion of chromosome 12p in a boy with developmental delay and congenital anomalies.
    Gläser B; Rossier E; Barbi G; Chiaie LD; Blank C; Vogel W; Kehrer-Sawatzki H
    Am J Med Genet A; 2003 Jan; 116A(1):66-70. PubMed ID: 12476454
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Deletion of chromosome region 18q21.1 --> 18q21.3 in a patient without clinical features of the 18q- phenotype.
    Engelen JJ; Moog U; Weber J; Haagen AA; van Uum CM; Hamers AJ
    Am J Med Genet A; 2003 Jun; 119A(3):356-9. PubMed ID: 12784305
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Deletion of proximal 6q: a clinical report and review of the literature.
    Yamamoto Y; Okamoto N; Shiraishi H; Yanagisawa M; Kamoshita S
    Am J Med Genet; 1986 Nov; 25(3):467-71. PubMed ID: 3789009
    [TBL] [Abstract][Full Text] [Related]  

  • 15. New insights into the phenotypes of 6q deletions.
    Hopkin RJ; Schorry E; Bofinger M; Milatovich A; Stern HJ; Jayne C; Saal HM
    Am J Med Genet; 1997 Jun; 70(4):377-86. PubMed ID: 9182778
    [TBL] [Abstract][Full Text] [Related]  

  • 16. De novo interstitial deletion q16.2q21 on chromosome 6.
    Villa A; Urioste M; Bofarull JM; Martínez-Frías ML
    Am J Med Genet; 1995 Jan; 55(3):379-83. PubMed ID: 7726240
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Relatively mild phenotype in a patient with interstitial 6q24.3-q25.2 deletion.
    Tanteles GA; Yates K; Martin K; Suri M
    Clin Dysmorphol; 2007 Apr; 16(2):101-104. PubMed ID: 17351353
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Ophthalmologic abnormalities in a de novo terminal 6q deletion.
    Abu-Amero KK; Hellani A; Salih MA; Al Hussain A; al Obailan M; Zidan G; Alorainy IA; Bosley TM
    Ophthalmic Genet; 2010 Mar; 31(1):1-11. PubMed ID: 20141352
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Isolated 6q terminal deletions: an emerging new syndrome.
    Bertini V; De Vito G; Costa R; Simi P; Valetto A
    Am J Med Genet A; 2006 Jan; 140(1):74-81. PubMed ID: 16329114
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Chromosome 6q deletions: a report of two additional cases and a review of the literature.
    McLeod DR; Fowlow SB; Robertson A; Samcoe D; Burgess I; Hoo JJ
    Am J Med Genet; 1990 Jan; 35(1):79-84. PubMed ID: 2405671
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 12.