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 *

130 related articles for article (PubMed ID: 5587668)

  • 1. Short arm deletion of chromosome 18.
    Kasahara S; Reisman LE
    Tohoku J Exp Med; 1967 Nov; 93(3):291-300. PubMed ID: 5587668
    [No Abstract]   [Full Text] [Related]  

  • 2. Trisomy 18.
    James AE; Belcourt CL; Atkins L; Janower ML
    Radiology; 1969 Jan; 92(1):37-43. PubMed ID: 4236175
    [No Abstract]   [Full Text] [Related]  

  • 3. Absence of IgA and growth hormone deficiency associated with short arm deletion of chromosome 18.
    Leisti J; Leisti S; Perheentupa J; Savilahti E; Aula P
    Arch Dis Child; 1973 Apr; 48(4):320-2. PubMed ID: 4705937
    [No Abstract]   [Full Text] [Related]  

  • 4. Short-arm deletion, chromosome 4, (4p-), a syndrome?
    Taylor AI; Challacombe DN; Howlett RM
    Ann Hum Genet; 1970 Oct; 34(2):137-44. PubMed ID: 5493842
    [No Abstract]   [Full Text] [Related]  

  • 5. 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]  

  • 6. A patient with a short arm deletion of chromosome 18 (46,XY,18p-).
    Weiss L; Mayeda K
    J Med Genet; 1969 Jun; 6(2):216-9. PubMed ID: 5801470
    [No Abstract]   [Full Text] [Related]  

  • 7. Trisomy 13-15.
    James AE; Belcourt CL; Atkins L; Janower ML
    Radiology; 1969 Jan; 92(1):44-9. PubMed ID: 4302761
    [No Abstract]   [Full Text] [Related]  

  • 8. 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]  

  • 9. Short arm deletion of chromosome 14.
    Emerit I; Noel B; Thiriet M; Loubon M; Quack B
    Humangenetik; 1972; 15(1):33-8. PubMed ID: 5046906
    [No Abstract]   [Full Text] [Related]  

  • 10. A short, retarded child with a deletion of the short arm of chromosome 18 (18p-).
    Parker CE; Donnell GN; Mavalwala J; Hurst N; Derencsenyi A
    Clin Pediatr (Phila); 1973 Jan; 12(1):42-6. PubMed ID: 4345621
    [No Abstract]   [Full Text] [Related]  

  • 11. [The clinical features of the 18 q-syndrome (author's transl)].
    Feichtinger C; Glatzl J
    Wien Klin Wochenschr; 1974 Aug; 86(15):441-4. PubMed ID: 4605988
    [No Abstract]   [Full Text] [Related]  

  • 12. A structurally abnormal chromosome (46,XX,?17p+) associated with mental deficiency and congenital malformations.
    Ricci N; Dallapiccola B; Ventimiglia B
    J Med Genet; 1968 Sep; 5(3):220-3. PubMed ID: 5708027
    [No Abstract]   [Full Text] [Related]  

  • 13. A mentally retarded child with a translocation involving chromosomes 12 and 19.
    Histinx TW; Gabreƫls FJ; Rutten FJ; Korten II; Scheres JM; Joosten EM
    J Med Genet; 1975 Jun; 12(2):207-10. PubMed ID: 1142383
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Agenesis of the corpus callosum with mosaicism 46,XY/47,XY, extra ring chromosome.
    Zamboni G; Bernardi F; Danesino C; del Majno UM; Beghini G; Dalla Bernardina B
    J Med Genet; 1980 Feb; 17(1):59-61. PubMed ID: 7365765
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. 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]  

  • 17. 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]  

  • 18. Ring chromosome 14 complicated with complex partial seizures and hypoplastic corpus callosum.
    Ono J; Nishiike K; Imai K; Otani K; Okada S
    Pediatr Neurol; 1999 Jan; 20(1):70-2. PubMed ID: 10029266
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. [Skeletal malformations caused by chromosome aberrations. Clinical and radiological study].
    Dallapiccola B; Pistocchi GF
    Minerva Med; 1972 Dec; 63(92):5049-208. PubMed ID: 4264793
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 7.