BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

134 related articles for article (PubMed ID: 14597381)

  • 1. Severe sensory hearing loss in del(6q)-syndrome.
    Schuster M; Lohscheller J; Kummer P; Eysholdt U; Rosanowski F
    Int J Pediatr Otorhinolaryngol; 2003 Nov; 67(11):1263-6. PubMed ID: 14597381
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Severe hearing loss in Pallister-Killian syndrome.
    Schuster M; Hoppe U; Eysholdt U; Rosanowski F
    ORL J Otorhinolaryngol Relat Spec; 2002; 64(5):343-5. PubMed ID: 12417777
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Distal monosomy of the long arm of chromosome 6 (6q25----6qter) inherited by maternal translocation t(6q;17q).
    Oliveira-Duarte MH; Martelli-Soares LR; Sarquis-Cintra T; Machado ML; Lison MP
    Ann Genet; 1990; 33(1):56-9. PubMed ID: 2195984
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. Partial 6q monosomy/partial 12q trisomy in a child with features of Kabuki make-up syndrome.
    Jardine PE; Burvill-Holmes LC; Schutt WH; Lunt PW
    Clin Dysmorphol; 1993 Jul; 2(3):269-73. PubMed ID: 8287190
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Prenatal diagnosis of a de novo trisomy 6q22.2-->6qter and monosomy 1pter-->1p36.3. Case report with a 2-year follow-up and a brief review of other prenatal cases of partial trisomy 6q.
    Kulharya AS; Carlin ME; Stettler RW; Huslig M; Kukolich MK; Garcia-Heras J
    Clin Genet; 1997 Feb; 51(2):115-7. PubMed ID: 9111999
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Terminal deletion of the long arm of chromosome 10: a new case with breakpoint in q25.3.
    Petersen B; Strassburg HM; Feichtinger W; Kress W; Schmid M
    Am J Med Genet; 1998 Apr; 77(1):60-2. PubMed ID: 9557896
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 6q1 monosomy: a distinctive syndrome.
    Turleau C; Demay G; Cabanis MO; Lenoir G; de Grouchy J
    Clin Genet; 1988 Jul; 34(1):38-42. PubMed ID: 3409537
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Monosomy 6q: report on four new cases.
    Valtat C; Galliano D; Mettey R; Toutain A; Moraine C
    Clin Genet; 1992 Mar; 41(3):159-66. PubMed ID: 1563091
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Retinoschisis and hyperopia associated with partial monosomy of 6q and partial trisomy of 11q.
    Bagheri N; Bahl RS; Singh AD; Rychwalski PJ
    Ophthalmic Genet; 2014 Jun; 35(2):107-11. PubMed ID: 24251586
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. Deletion of the long arm of chromosome 6: two new patients and literature review.
    Evers LJ; Schrander-Stumpel CT; Engelen JJ; Hoorntje TM; Pulles-Heintzberger CF; Schrander JJ; Albrechts JC; Peters J; Fryns JP
    Clin Genet; 1996 Sep; 50(3):138-44. PubMed ID: 8946112
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. Monosomy 6q1: syndrome delineation.
    Romie SS; Hartsfield JK; Sutcliffe MJ; Dumont DP; Kousseff BG
    Am J Med Genet; 1996 Mar; 62(2):105-8. PubMed ID: 8882389
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Terminal deletion of chromosome 6q.
    Su PH; Chen JY; Chen SJ; Yang KC
    Pediatr Neonatol; 2008 Jun; 49(3):88-93. PubMed ID: 18947005
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Partial trisomy 6q: case report with necropsy findings.
    Franchino CJ; Beneck D; Greco MA; Wolman SR
    J Med Genet; 1987 May; 24(5):300-3. PubMed ID: 3585945
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Monosomy 5 (-5), deletion of the long arm of chromosome 6 (6q) and acquisition of a chromosome 21 (+21) in a boy with acute leukemia at high-risk].
    Burattini MG; Santoro N; Spano M; Aufiero T; Schettini F
    Minerva Pediatr; 1989 Jul; 41(7):379-82. PubMed ID: 2601656
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Deletions of the long arm of chromosome 6: two new cases and review of the literature.
    Young RS; Fidone GS; Reider-Garcia PA; Hansen KL; McCombs JL; Moore CM
    Am J Med Genet; 1985 Jan; 20(1):21-9. PubMed ID: 3881954
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Sensorineural deafness in two infants: a novel feature in the 22q distal duplication syndrome. Cardinal signs in trisomies 22 subtypes.
    Barajas-Barajas LO; Valdez LL; Gonzalez JR; García-García C; Rivera H; Ramírez L
    Genet Couns; 2004; 15(2):167-73. PubMed ID: 15287416
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A child with partial monosomy 6q secondary to a maternal direct insertional event.
    Matkins SV; Meyer JE; Berry AC
    J Med Genet; 1987 Apr; 24(4):227-9. PubMed ID: 3585939
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.