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 *

171 related articles for article (PubMed ID: 5518460)

  • 1. 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]  

  • 2. Case report. Familial 4-22 translocation with partial trisomy for the short arm of chromosome 4 in two sibs.
    Sartori A; Tenconi R; Baccichetti C; Pujatti G
    Acta Paediatr Scand; 1974 Jul; 63(4):631-5. PubMed ID: 4850900
    [No Abstract]   [Full Text] [Related]  

  • 3. Cytogenetics in mentally defective children with anomalies: a controlled study.
    Summitt RL
    J Pediatr; 1969 Jan; 74(1):58-66. PubMed ID: 5782825
    [No Abstract]   [Full Text] [Related]  

  • 4. 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]  

  • 5. 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]  

  • 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. 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]  

  • 8. An unusual balanced reciprocal translocation in several members of a family.
    Monteleone PL; Monteleone JA; Grzegocki J
    J Med Genet; 1969 Dec; 6(4):394-8. PubMed ID: 5365947
    [No Abstract]   [Full Text] [Related]  

  • 9. Developmental abnormalities in a patient with karyotype 46,XX,bq+.
    Chakanovskis JE; Sutherland GR
    J Med Genet; 1970 Jun; 7(2):180-4. PubMed ID: 5519607
    [No Abstract]   [Full Text] [Related]  

  • 10. An extra small metacentric chromosome in association with multiple congenital abnormalities.
    Finley WH; Finley SC; Monsky D
    J Med Genet; 1971 Sep; 8(3):381-3. PubMed ID: 5097148
    [No Abstract]   [Full Text] [Related]  

  • 11. 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]  

  • 12. Karyotype with chromosomal abnormality with various inherited defects in the offspring (recombination aneusomy).
    Warter S; Ruch JV; Lehmann M
    Humangenetik; 1973 Dec; 20(4):355-9. PubMed ID: 4768111
    [No Abstract]   [Full Text] [Related]  

  • 13. Human congenital abnormalities associated with a long group B chromosome.
    Holden HE
    J Hered; 1971; 62(6):380-1. PubMed ID: 5137684
    [No Abstract]   [Full Text] [Related]  

  • 14. Ring chromosome 18 in a patient with multiple anomalies.
    Palmer CG; Fareed N; Merritt AD
    J Med Genet; 1967 Jun; 4(2):117-23. PubMed ID: 5619991
    [No Abstract]   [Full Text] [Related]  

  • 15. Unbalanced X-autosomal translocation with inactivation of the normal X chromosome.
    Mikkelsen M; Dahl G
    Cytogenet Cell Genet; 1973; 12(5):357-66. PubMed ID: 4131091
    [No Abstract]   [Full Text] [Related]  

  • 16. A homozygote for pericentric inversion of chromosome 4.
    Carpenter NJ; Say B; Barber ND
    J Med Genet; 1982 Dec; 19(6):469-71. PubMed ID: 6185681
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. Chromosome aberrations in 50 patients with idiopathic mental retardation and in 50 control subjects. Madison blind study 3.
    Daly RF
    J Pediatr; 1970 Sep; 77(3):444-53. PubMed ID: 5502094
    [No Abstract]   [Full Text] [Related]  

  • 19. Ring-G chromosome, a new G-deletion syndrome?
    Weleber RG; Hecht F; Giblett ER
    Am J Dis Child; 1968 Apr; 115(4):489-93. PubMed ID: 4296014
    [No Abstract]   [Full Text] [Related]  

  • 20. Tertiary trisomy in a human kindred containing an E/G translocation.
    Macintyre MN; Walden DB; Hempel JM
    Am J Hum Genet; 1971 Sep; 23(5):431-41. PubMed ID: 5092595
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 9.