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 *

235 related articles for article (PubMed ID: 5149534)

  • 1. 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]  

  • 2. 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]  

  • 3. Mosaicism with translocation: autoradiographic and fluorescent studies of an inherited reciprocal translocation t(2q+;14q-).
    Reiss JA; Wyandt HE; Magenis RE; Lovrien EW; Hecht F
    J Med Genet; 1972 Sep; 9(3):280-6. PubMed ID: 5079098
    [No Abstract]   [Full Text] [Related]  

  • 4. A case of 46,XY,t(1;13) (q24;q32) with mental retardation.
    Wilbur L; Curcuru-Giordano FM; Krishna SG; Kardon NB; Jenkins EC
    Hum Genet; 1977 Jun; 37(2):239-42. PubMed ID: 885541
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Study of a patient with apparent monosomy 21 owing to translocation: 45,XX,21-,t(18q+).
    Wyandt HE; Hecht F; Lovrien EW; Stewart RE
    Cytogenetics; 1971; 10(6):413-26. PubMed ID: 5146418
    [No Abstract]   [Full Text] [Related]  

  • 6. Duplication deficiency syndrome in familial translocation (2q-;5p+).
    Bijlsma JB; de France H; Bleeker-Wagemakers EM
    Humangenetik; 1971; 12(2):110-22. PubMed ID: 5568729
    [No Abstract]   [Full Text] [Related]  

  • 7. Inherited t(13q14q) in two retarded sisters.
    Crandall BF; Francke U; Campbell MA; Sparkes RS
    Am J Hum Genet; 1972 Jul; 24(4):416-24. PubMed ID: 5031981
    [No Abstract]   [Full Text] [Related]  

  • 8. A ring chromosome (46,XY,13r) occurring in a family with a D-D translocation 13-,14-, t(13q 14q).
    Mikkelsen M; Niebuhr E
    Ann Genet; 1969 Mar; 12(1):51-6. PubMed ID: 5306712
    [No Abstract]   [Full Text] [Related]  

  • 9. Trisomy of the short arm of chromosome 8: association with translocation between chromosomes 8 and 22 46,XY,22-,t(8p22q) plus.
    Rosenthal IM; Krmpotic E; Bocian M; Szego K
    Clin Genet; 1973 Jun; 4(6):507-16. PubMed ID: 4787842
    [No Abstract]   [Full Text] [Related]  

  • 10. 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]  

  • 11. Placental chorangiomata and mental deficiency in a child with 2/15 translocation: 46,XX,t(2q-;15q+).
    Wurster DH; Hoefnagel D; Benirschke K; Allen FH
    Cytogenetics; 1969; 8(5):389-99. PubMed ID: 5823571
    [No Abstract]   [Full Text] [Related]  

  • 12. A partial D-trisomy-normal mosaic female.
    Webb GC; Garson M; Robson MK; Pitt DB
    J Med Genet; 1971 Dec; 8(4):522-7. PubMed ID: 5149538
    [No Abstract]   [Full Text] [Related]  

  • 13. A family showing transmission of a translocation t(3porq-;Cq+).
    McHugh J; Wright T; Cooke P
    J Med Genet; 1971 Dec; 8(4):509-12. PubMed ID: 5149535
    [No Abstract]   [Full Text] [Related]  

  • 14. Banding identification of chromosomal abnormalities in four patients: ring (6), translocation (2q-;15q+), translocation (21q;21q) and deletion (22q-).
    Wurster-Hill DH; Hoefnagel D
    J Ment Defic Res; 1975 Jun; 19(2):145-50. PubMed ID: 127842
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A girl with 46,XX,t(1;15) karyotype. Cytogenetic and clinical observations.
    van Hemel JO; van Biervliet JP; de Jager-van der Grift PW
    Clin Genet; 1975 Sep; 8(3):213-7. PubMed ID: 1175325
    [No Abstract]   [Full Text] [Related]  

  • 16. 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]  

  • 17. Severe mental retardation in a boy with partial trisomy 10q and partial monosomy 2q.
    Sills JA; Buckton KE; Raeburn JA
    J Med Genet; 1976 Dec; 13(6):507-10. PubMed ID: 1018309
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Pericentric inversions of chromosome 9 in two families.
    Wahrman J; Atidia J; Goitein R; Cohen T
    Cytogenetics; 1972; 11(2):132-44. PubMed ID: 5024689
    [No Abstract]   [Full Text] [Related]  

  • 19. MN blood-group locus: data concerning the possible chromosomal location.
    German J; Walker ME; Stiefel FH; Allen FH
    Science; 1968 Nov; 162(3857):1014-5. PubMed ID: 5698839
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A case of multople chromosomal rearrangements with persistence of foetal haemoglobin.
    Nuzzo F; Marini A; Baglioni C; Ford CE; De Carli L; Piceni Sereni L
    Cytogenetics; 1968; 7(3):169-82. PubMed ID: 5682897
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 12.