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: 2369070)

  • 41. [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]  

  • 42. Sub-band deletion of 7q36.3 in a patient with ring chromosome 7: association with holoprosencephaly.
    Sawyer JR; Lukacs JL; Hassed SJ; Arnold GL; Mitchell HF; Muenke M
    Am J Med Genet; 1996 Oct; 65(2):113-6. PubMed ID: 8911601
    [TBL] [Abstract][Full Text] [Related]  

  • 43. Decreased cell viability of fibroblasts from two patients with a ring chromosome: an in vitro reflection of growth failure?
    Kosztolányi G
    Am J Med Genet; 1987 Sep; 28(1):181-4. PubMed ID: 3674110
    [TBL] [Abstract][Full Text] [Related]  

  • 44. Jumping translocation in a newborn boy with dup(4q) and severe hydrops fetalis.
    Duval E; van den Enden A; Vanhaesebrouck P; Speleman F
    Am J Med Genet; 1994 Aug; 52(2):214-7. PubMed ID: 7802011
    [TBL] [Abstract][Full Text] [Related]  

  • 45. [Roberts' syndrome. Review of the literature and presentation of 2 clinical cases].
    Colombo B; Bottelli A; Maserati E
    Pediatr Med Chir; 1986; 8(3):411-3. PubMed ID: 3786205
    [TBL] [Abstract][Full Text] [Related]  

  • 46. Interstitial deletion of chromosome 1 del (1) (q32 q42): case report and review of the literature.
    Sarda P; Lefort G; Taviaux S; Humeau C; Rieu D
    Clin Genet; 1992 Jan; 41(1):25-7. PubMed ID: 1633642
    [TBL] [Abstract][Full Text] [Related]  

  • 47. Isochromosome 12p mosaicism (Pallister mosaic aneuploidy or Pallister-Killian syndrome): report of 11 cases.
    Reynolds JF; Daniel A; Kelly TE; Gollin SM; Stephan MJ; Carey J; Adkins WN; Webb MJ; Char F; Jimenez JF
    Am J Med Genet; 1987 Jun; 27(2):257-74. PubMed ID: 3605212
    [TBL] [Abstract][Full Text] [Related]  

  • 48. The cytogenetic and clinical implications of a ring chromosome 2.
    Cote GB; Katsantoni A; Deligeorgis D
    Ann Genet; 1981; 24(4):231-5. PubMed ID: 6977305
    [TBL] [Abstract][Full Text] [Related]  

  • 49. Clinical findings and cytogenetic analysis of small supernumerary ring chromosomes 7: report of two new cases.
    Chantot-Bastaraud S; Muti C; Pipiras E; Routon MC; Roubergue A; Burglen L; Siffroi JP; Simon-Bouy B
    Ann Genet; 2004; 47(3):241-9. PubMed ID: 15337469
    [TBL] [Abstract][Full Text] [Related]  

  • 50. [Two cases of 18q- syndrome with mosaicism (46,XX / 46,XX, 18q-)].
    Lejeune J; Berger R; Réthoré MO; Lafourcade J; Dutrillaux B; Canlorbe P; Labrune B
    Ann Genet; 1967 Mar; 10(1):18-24. PubMed ID: 5300122
    [No Abstract]   [Full Text] [Related]  

  • 51. Iris coloboma, ptosis, hypertelorism, and mental retardation: a new syndrome possibly localised on chromosome 2.
    Pallotta R
    J Med Genet; 1991 May; 28(5):342-4. PubMed ID: 1865474
    [TBL] [Abstract][Full Text] [Related]  

  • 52. [Rethoré syndrome (9p trisomy) with unusual karyotype: 46,XX,-9, + der 9p, t(9;9)mat].
    Di Cesare D; Paludetto R; Casullo C; Pagano L; Stabile M; Sicolo A; Ventruto V
    Minerva Pediatr; 1980 Dec; 32(23):1349-52. PubMed ID: 7219376
    [No Abstract]   [Full Text] [Related]  

  • 53. [Prenatal diagnosis of 3 cases of ring G chromosomes: one 21 and two 22, one of which was de novo].
    Crusi A; Engel E
    Ann Genet; 1986; 29(4):253-60. PubMed ID: 3495227
    [TBL] [Abstract][Full Text] [Related]  

  • 54. Complex familial rearrangement of chromosome 9p24.3 detected by FISH.
    Repetto GM; Wagstaff J; Korf BR; Knoll JH
    Am J Med Genet; 1998 Apr; 76(4):306-9. PubMed ID: 9545094
    [TBL] [Abstract][Full Text] [Related]  

  • 55. [Ring chromosome 14. I. A case report on homogeneous r(14)].
    Raoul O; Razavi F; Lescs MC; Bouhanna A
    Ann Genet; 1984; 27(2):88-90. PubMed ID: 6331795
    [TBL] [Abstract][Full Text] [Related]  

  • 56. Phenotype associated with ring 10 chromosome: report of patient and review of literature.
    Michels VV; Driscoll DJ; Ledbetter DH; Riccardi VM
    Am J Med Genet; 1981; 9(3):231-7. PubMed ID: 7025632
    [TBL] [Abstract][Full Text] [Related]  

  • 57. Ring chromosome 11. A case report and review of the literature.
    Palka G; Verrotti A; Peca S; Mosca L; Lombardo G; Verrotti M; Morgese G
    Ann Genet; 1986; 29(1):55-8. PubMed ID: 3487279
    [TBL] [Abstract][Full Text] [Related]  

  • 58. [Ring chromosome 18].
    Andersen UM
    Ugeskr Laeger; 1992 Nov; 154(46):3250-1. PubMed ID: 1462429
    [TBL] [Abstract][Full Text] [Related]  

  • 59. Apparent monosomy 21 owing to a ring 21 chromosome: parental origin revealed by DNA analysis.
    Dalgleish R; Duckett DP; Woodhouse M; Shannon RS; Young ID
    J Med Genet; 1988 Dec; 25(12):851-4. PubMed ID: 3236369
    [TBL] [Abstract][Full Text] [Related]  

  • 60. The occurrence of a ring 18, an accessory bisatellited fragment, and trisomy 21 within one sibship.
    Grace E; Sills J
    Hum Genet; 1978 Jul; 43(1):111-4. PubMed ID: 149756
    [TBL] [Abstract][Full Text] [Related]  

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