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 *

128 related articles for article (PubMed ID: 6078180)

  • 61. Partial trisomy 9q due to maternal 9/17 translocation.
    Aftimos SF; Hoo JJ; Parslow MI
    Am J Dis Child; 1980 Sep; 134(9):848-50. PubMed ID: 7416109
    [TBL] [Abstract][Full Text] [Related]  

  • 62. Cytogenetic and clinical studies in five cases of inv dup(15).
    Wisniewski L; Hassold T; Heffelfinger J; Higgins JV
    Hum Genet; 1979 Sep; 50(3):259-70. PubMed ID: 489010
    [TBL] [Abstract][Full Text] [Related]  

  • 63. Letter: D-group chromosomal aberration: 13q+.
    Hayes TG; Del Rosario AJ
    Lancet; 1973 Nov; 2(7839):1215. PubMed ID: 4127597
    [No Abstract]   [Full Text] [Related]  

  • 64. Letter: Brilliantly fluorescing enlarged short arms D or G.
    Nielsen J; Friedrich U; Hreidarsson AB; Noel B; Quack B; Mottet J
    Lancet; 1974 May; 1(7865):1049-50. PubMed ID: 4133722
    [No Abstract]   [Full Text] [Related]  

  • 65. Translocation, t(4qminus;13qplus), in three generations resulting in partial trisomy of the long arm of chromosome 4 in the fourth generation.
    Schrott HG; Sakaguchi S; Francke U; Luzzatti L; Fialkow PJ
    J Med Genet; 1974 Jun; 11(2):201-5. PubMed ID: 4135220
    [TBL] [Abstract][Full Text] [Related]  

  • 66. Inherited chromosomal translocation in two families (t(4q-;13q+) and t(5q-; 13q+)).
    Watanabe G; Kiyoi Y; Takeyama I; Kawana S; Yamamoto M
    Tohoku J Exp Med; 1977 Feb; 121(2):179-84. PubMed ID: 847744
    [TBL] [Abstract][Full Text] [Related]  

  • 67. [Mental retardation and sexual development in chromosomal syndrome (author's transl)].
    Balestrazzi P; Bernasconi S; Medioli FC; Corrini L; Villani G
    Ateneo Parmense Acta Biomed; 1980; 51(1):45-51. PubMed ID: 7470180
    [TBL] [Abstract][Full Text] [Related]  

  • 68. A recognizable phenotype in a child with partial duplication 13q in a family with t(10q;13q).
    Hornstein L; Soukup S
    Clin Genet; 1981 Feb; 19(2):81-6. PubMed ID: 7471511
    [TBL] [Abstract][Full Text] [Related]  

  • 69. A mentally retarded child convulsions, agenesis of the corpus callosum, and a translocation involving chromosomes 2 and the B group.
    Mantle DJ; Mitchell P; Kucheria K; Wilson J
    J Med Genet; 1969 Dec; 6(4):435-7. PubMed ID: 5365953
    [No Abstract]   [Full Text] [Related]  

  • 70. Choanal atresia and bifid thumb associated with an abnormal D group chromosome.
    Carter CH; Smith GF; Schindeler J
    J Ment Defic Res; 1970 Sep; 14(3):221-6. PubMed ID: 5518407
    [No Abstract]   [Full Text] [Related]  

  • 71. De novo translocation involving chromosomes 2, 8, and 20.
    Zaletajev DV; Marincheva GS; Tsvetkova TG
    J Med Genet; 1984 Jun; 21(3):231. PubMed ID: 6748024
    [No Abstract]   [Full Text] [Related]  

  • 72. Wolf-Hirschhorn syndrome and balanced (4;10) translocation in the father.
    Hedner K; Carlsson E; Mitelman F
    Clin Genet; 1977 Aug; 12(2):101-3. PubMed ID: 891010
    [No Abstract]   [Full Text] [Related]  

  • 73. New cytogenetic variant of Orbeli's syndrome (46,XY-45,XY,-D-46,XY,Dq+).
    Lazjuk GI; Lurie IW; Kravtzova GI; Usoev SS
    Humangenetik; 1973 Dec; 20(3):219-21. PubMed ID: 4772075
    [No Abstract]   [Full Text] [Related]  

  • 74. The 4p-syndrome, with a report of two new cases.
    Fryns JP; Eggermont E; Verresen H; Van den Berghe H
    Humangenetik; 1973; 19(1):99-109. PubMed ID: 4725911
    [No Abstract]   [Full Text] [Related]  

  • 75. Autosomal chromosome aberrations in ophthalmology.
    François J
    J Neurol Sci; 1967; 4(3):511-58. PubMed ID: 4228074
    [No Abstract]   [Full Text] [Related]  

  • 76. Enlargement of the long arm of a B-group chromosome (Bq+) in a boy aged nine years.
    Revazov AA; Derilo TG; Vorsanova SG
    Sov Genet; 1973 Dec; 7(8):1086-9. PubMed ID: 4783223
    [No Abstract]   [Full Text] [Related]  

  • 77. Partial trisomy 11 in a child resulting from a complex maternal rearrangement of chromosomes 11, 12 and 13.
    Sanchez O; Yunis JJ; Escobar JI
    Humangenetik; 1974 Apr; 22(1):59-65. PubMed ID: 4134840
    [No Abstract]   [Full Text] [Related]  

  • 78. [Familial translocation t(3;22) detected in a carrier child with mental retardation and other abnormalities].
    Gregori Romero M; Gil Benso R; López Ginés C; Pellín Pérez A; Barberá Guillem E
    An Esp Pediatr; 1984 Oct; 21(6):593-6. PubMed ID: 6524770
    [TBL] [Abstract][Full Text] [Related]  

  • 79. Autosomal syndromes.
    Summitt RL
    Pediatr Ann; 1978 Jun; 7(6):94-5, 97-100, 102-7 passim. PubMed ID: 149945
    [No Abstract]   [Full Text] [Related]  

  • 80. A familial extra small marker autosome in persons with normal phenotype.
    Fried K; Rosenblatt M
    Hum Hered; 1979; 29(6):371-3. PubMed ID: 511193
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.