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 *

230 related articles for article (PubMed ID: 7241544)

  • 1. Inheritance of a ring 14 chromosome.
    Riley SB; Buckton KE; Ratcliffe SG; Syme J
    J Med Genet; 1981 Jun; 18(3):209-13. PubMed ID: 7241544
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Ring (15) chromosome.
    Yunis E; Leibovici M; Quintero L
    Hum Genet; 1981; 57(2):207-9. PubMed ID: 7228035
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Chromosome 15 abnormality in a mentally retarded adult.
    Kelly S; Almy R; Dagle A
    J Med Genet; 1969 Dec; 6(4):438-41. PubMed ID: 5365954
    [No Abstract]   [Full Text] [Related]  

  • 4. Ring chromosome 14 in a mentally retarded girl.
    Iselius L; Ritzén M; Bui TH; Olsson K; Eklöf O
    Acta Paediatr Scand; 1980 Nov; 69(6):803-6. PubMed ID: 7211367
    [TBL] [Abstract][Full Text] [Related]  

  • 5. t(2q-; Dq+) in a mentally retarded female child.
    Davison BC; Bedford J; Dunn W
    J Med Genet; 1970 Mar; 7(1):81-2. PubMed ID: 5480969
    [No Abstract]   [Full Text] [Related]  

  • 6. Tandem duplication (5q13 to 22) in a mentally deficient girl.
    Kessel E; Pfeiffer RA
    Hum Genet; 1979 Nov; 52(2):217-20. PubMed ID: 511177
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Familial 13p+ chromosome with mental retardation and dysmorphic features of two children.
    Stoll C; Rohmer A; Korn R; Heumann G
    Hum Genet; 1976 Sep; 34(1):81-4. PubMed ID: 965011
    [TBL] [Abstract][Full Text] [Related]  

  • 8. An (11;21) translocation in four generations with chromosome 11 abnormalities in the offspring. A clinical, cytogenetical, and gene marker study.
    Jacobsen P; Hauge M; Henningsen K; Hobolth N; Mikkelsen M; Philip J
    Hum Hered; 1973; 23(6):568-85. PubMed ID: 4134631
    [No Abstract]   [Full Text] [Related]  

  • 9. A complex four-break rearrangement between chromosomes 4 and 13 resulting in a recombinant chromosome 4.
    Andersen O; Lundsteen C; Niebuhr E
    Cytogenet Cell Genet; 1981; 30(1):3-10. PubMed ID: 7261680
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Inherited partial duplication of chromosome No. 15.
    Fujimoto A; Towner JW; Ebbin AJ; Kahlstrom EJ; Wilson MG
    J Med Genet; 1974 Sep; 11(3):287-91. PubMed ID: 4139262
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Partial monosomy and partial trisomy for different segments of chromosome 13 in several individuals of the same family.
    Wilroy RS; Summitt RL; Martens P; Gooch WM
    Ann Genet; 1977 Dec; 20(4):237-42. PubMed ID: 305749
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. [Translocation of a part of the long arms of chromosome 5 on the long arms of a D group chromosome (Bq-,Dq+) in a child and its mother].
    Rumpler Y; Ruch JV; Beauvais P
    Humangenetik; 1967; 4(2):166-73. PubMed ID: 6078180
    [No Abstract]   [Full Text] [Related]  

  • 14. Cytogenetic study of a 5-14 translocation in man.
    Borgaonkar DS; Blair SM; Lutz JB; Kelly T; Tice RR; Delaney NV; Hutchinson JR; Bias WB
    J Hered; 1973; 64(5):299-300. PubMed ID: 4782671
    [No Abstract]   [Full Text] [Related]  

  • 15. Autosomal translocation in a mentally retarded male child with 46,XY,t(2q-;13q+) complement. Case report and review.
    Genest P; Lachance R; Poty J; Jacob D
    J Med Genet; 1971 Dec; 8(4):504-8. PubMed ID: 5149534
    [No Abstract]   [Full Text] [Related]  

  • 16. Microcephaly, mental retardation and hypertelorism in chromosome deletion studies.
    Miller JQ
    Neurology; 1973 Nov; 23(11):1141-6. PubMed ID: 4795737
    [No Abstract]   [Full Text] [Related]  

  • 17. Ring chromosome 22 in a mentally retarded child and mosaic 45,XX,-15,-22,+t(15;22)(p11;q11)/46,XX,r(22)/46,XX karyotype in the mother.
    Fryns JP; Van den Berghe H
    Hum Genet; 1979 Mar; 47(2):213-6. PubMed ID: 437787
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Replication error, a new hypothesis to explain the origin of a supernumerary marker chromosome in a mentally retarded boy.
    Wik Sjöstedt A; Alatalo M; Wahlström J; von Döbeln U; Olegård R
    Hereditas; 1989; 111(2):115-23. PubMed ID: 2625404
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. An extra small metacentric chromosome in a mentally retarded boy.
    Ishmael J; Laurence KM
    J Med Genet; 1968 Dec; 5(4):335-40. PubMed ID: 5713650
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 12.