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 *

256 related articles for article (PubMed ID: 4296014)

  • 41. [A new case of a ring shaped chromosome 18 (18 r)].
    Petit P; Poncelet R
    Ann Genet; 1967 Sep; 10(3):134-7. PubMed ID: 5300397
    [No Abstract]   [Full Text] [Related]  

  • 42. Terminal deletion of the long arm of chromosome 4 in a mother and two sons.
    Descartes M; Keppler-Noreuil K; Knops J; Longshore JW; Finley WH; Carroll AJ
    Clin Genet; 1996 Dec; 50(6):538-40. PubMed ID: 9147894
    [TBL] [Abstract][Full Text] [Related]  

  • 43. Wolf-Hirschhorn syndrome associated with an unusual abnormality of chromosome no. 4.
    Wilson MG; Towner JW; Negus LD
    J Med Genet; 1970 Jun; 7(2):164-70. PubMed ID: 5519605
    [No Abstract]   [Full Text] [Related]  

  • 44. X-autosome translocation in normal mother and effectively 21-monosomic daughter.
    Summitt RL; Martens PR; Wilroy RS
    J Pediatr; 1974 Apr; 84(4):539-46. PubMed ID: 4834247
    [No Abstract]   [Full Text] [Related]  

  • 45. An inherited small extra chromosome: a mother with 46,XX,t(17;22)(pl;ql) and a son with 47,XY,+der(22)mat.
    Borgaonkar DS; McKusick VA; Farber PA
    J Med Genet; 1973 Dec; 10(4):379-84. PubMed ID: 4129973
    [TBL] [Abstract][Full Text] [Related]  

  • 46. Ring chromosome 6 in a malformed boy.
    Salamanca-Gonez F; Nava S; Armendares S
    Clin Genet; 1975 Nov; 8(5):370-5. PubMed ID: 1204234
    [TBL] [Abstract][Full Text] [Related]  

  • 47. Case report of an extra, small, acrocentric chromosome in a non-mongoloid girl.
    Kaijser K
    Clin Genet; 1974; 5(3):254-8. PubMed ID: 4838893
    [No Abstract]   [Full Text] [Related]  

  • 48. [Abnormal C group chromosome in several members of the same family].
    Emerit I; Vernant P
    Humangenetik; 1968; 6(4):326-34. PubMed ID: 5713618
    [No Abstract]   [Full Text] [Related]  

  • 49. Inherited pericentric inversion of chromosome no. 4.
    Wilson MG; Towner JW; Coffin GS; Forsman I
    Am J Hum Genet; 1970 Nov; 22(6):679-90. PubMed ID: 5518460
    [No Abstract]   [Full Text] [Related]  

  • 50. [A case with mosaicism of partial monosomy G- monosomy G in peripheral blood lymphocytes].
    Bauchinger M; Schmid E; Röttinger E
    Humangenetik; 1968; 6(4):303-10. PubMed ID: 5713616
    [No Abstract]   [Full Text] [Related]  

  • 51. A human ring C chromosome associated with multiple congenital abnormalities.
    De Chieri PR; Albores JM; Cosín A; Cosín JM
    J Med Genet; 1972 Jun; 9(2):239-42. PubMed ID: 5046637
    [No Abstract]   [Full Text] [Related]  

  • 52. Chromosome banding patterns in an infant with 13q minus syndrome.
    Ikeuchi T; Sonta S; Sasaki M; Hujita M; Tsunematsu K
    Humangenetik; 1974 Mar; 21(4):309-14. PubMed ID: 4134627
    [No Abstract]   [Full Text] [Related]  

  • 53. Indications for chromosome analysis illustrated by a case of ring 22.
    Howard-Peebles PN
    J Hered; 1977; 68(4):268-9. PubMed ID: 411817
    [TBL] [Abstract][Full Text] [Related]  

  • 54. Deletion of the short arm of chromosome No. 10.
    Shokeir MH; Ray M; Hamerton JL; Bauder F; O'Brien H
    J Med Genet; 1975 Mar; 12(1):99-103. PubMed ID: 47396
    [TBL] [Abstract][Full Text] [Related]  

  • 55. A "G" deletion syndrome anti-mongolism.
    Richmond HG; MacArthur P; Hunter D
    Acta Paediatr Scand; 1973 Mar; 62(2):216-20. PubMed ID: 4691464
    [No Abstract]   [Full Text] [Related]  

  • 56. Human chromosomal deletion: two patients with the 4p- syndrome.
    Arias D; Passarge E; Engle MA; German J
    J Pediatr; 1970 Jan; 76(1):82-8. PubMed ID: 5410164
    [No Abstract]   [Full Text] [Related]  

  • 57. [Monosomy 21 with mosaicism 45,XX,21--46,XX,21 pi].
    Emberger JM; Rey J; Rieu D; Dossa D; Bonnet H; Jean R
    Arch Fr Pediatr; 1970; 27(10):1069-79. PubMed ID: 5495707
    [No Abstract]   [Full Text] [Related]  

  • 58. Monosomy G: case report and review of the literature.
    Greenwood RD; Sommer A
    J Med Genet; 1971 Dec; 8(4):496-500. PubMed ID: 5149533
    [No Abstract]   [Full Text] [Related]  

  • 59. [Observation of the 13-15 chromosome group in a ring (46,XY,15r)].
    Emberger JM; Rossi D; Jean R; Bonnet H; Dumas R
    Humangenetik; 1971; 11(4):295-9. PubMed ID: 5550594
    [No Abstract]   [Full Text] [Related]  

  • 60. Retinoblastoma and deletion D (14) syndrome.
    Wilson MG; Melnyk J; Towner JW
    J Med Genet; 1969 Sep; 6(3):322-7. PubMed ID: 5345106
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 13.