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 *

168 related articles for article (PubMed ID: 5747328)

  • 1. [Chromoosome 1 abnormality in a child with multiple malformations].
    Ernould C; Hausman-Hagemeijer A; Lecomte-Ramioul S; Geubelle F
    Acta Paediatr Belg; 1968; 22(6):403-16. PubMed ID: 5747328
    [No Abstract]   [Full Text] [Related]  

  • 2. A new recognizable syndrome associated with a chromosomal abnormality.
    Handmaker SD; Hall BD; Conte FA
    Birth Defects Orig Artic Ser; 1975; 11(5):181-9. PubMed ID: 1218211
    [No Abstract]   [Full Text] [Related]  

  • 3. [Cumulative developmental anomalies and the incidence of ring-chromosome (C) in one family].
    Gács G; Schuler D
    Orv Hetil; 1969 Aug; 110(32):1852-3. PubMed ID: 5809883
    [No Abstract]   [Full Text] [Related]  

  • 4. Ring chromosome 2 in a child with growth failure and few congenital abnormalities.
    Vigfusson NV; Kapstafer KJ; Lloyd MA
    Am J Med Genet; 1980; 7(3):383-9. PubMed ID: 7468662
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [46, XX, 1q-, 2q-, Dq+, 16q+ karyotype in a polymalformed child].
    de Grouchy J; Lautmann F
    Ann Genet; 1968 Jun; 11(2):129-31. PubMed ID: 5303425
    [No Abstract]   [Full Text] [Related]  

  • 6. Ring chromosome 15.
    Kiss P; Osztovics M
    Acta Paediatr Acad Sci Hung; 1982; 23(4):409-15. PubMed ID: 7170952
    [No Abstract]   [Full Text] [Related]  

  • 7. [Etiopathological classification of scoliosis I].
    Bellyei A; Czeizel E; Barta O; Magda T; Molnar L
    Orv Hetil; 1976 Oct; 117(41):2475-7. PubMed ID: 787890
    [No Abstract]   [Full Text] [Related]  

  • 8. [12 p trisomy. A new case (author's transl)].
    Kubryk N; Prieur M; Borde M
    Ann Pediatr (Paris); 1980 Dec; 27(10):695-9. PubMed ID: 7212558
    [No Abstract]   [Full Text] [Related]  

  • 9. Duplication 3q: severe manifestations in an infant with duplication of a short segment of 3q.
    Rosenfeld W; Verma RS; Jhaveri RC; Estrada R; Evans H; Dosik H
    Am J Med Genet; 1981; 10(2):187-92. PubMed ID: 7315875
    [TBL] [Abstract][Full Text] [Related]  

  • 10. The dup(3q) syndrome: report of eight cases and review of the literature.
    Steinbach P; Adkins WN; Caspar H; Dumars KW; Gebauer J; Gilbert EF; Grimm T; Habedank M; Hansmann I; Herrmann J; Kaveggia EG; Langenbeck U; Meisner LF; Najafzadeh TM; Opitz JM; Palmer CG; Peters HH; Scholz W; Tavares AS; Wiedeking C
    Am J Med Genet; 1981; 10(2):159-77. PubMed ID: 7315873
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Genetic prognosis of chromosome translocations].
    Srsen S; Volna J
    Cesk Pediatr; 1980 Apr; 35(4):196-203. PubMed ID: 7397898
    [No Abstract]   [Full Text] [Related]  

  • 12. [Multiple abnormalities in a newborn infant with a D1ring chromosome].
    Biles AR; Lüers T; Sperling K
    Med Welt; 1969 Aug; 33():1771-5. PubMed ID: 5357975
    [No Abstract]   [Full Text] [Related]  

  • 13. [Two cases of trisomy 13 with persistance of the embryonal hemoglobin Gower 2].
    Blum N; De Grouchy J; Alison F
    Ann Genet; 1967 Sep; 10(3):138-40. PubMed ID: 5300398
    [No Abstract]   [Full Text] [Related]  

  • 14. [A case of cyclopia in a sibling group presenting additionally several median malformations of the face].
    Ardouin M; Lanchou G; Faivre J; Garnier JP
    Rev Otoneuroophtalmol; 1968; 40(5):259-70. PubMed ID: 4988800
    [No Abstract]   [Full Text] [Related]  

  • 15. [Multiple malformations in a newborn infant presenting a chromosomic triploidy].
    Bernard R; Stahl A; Coignet J; Giraud F; Hartung M; Passeron P
    Pediatrie; 1967 Sep; 22(6):721-2. PubMed ID: 4312709
    [No Abstract]   [Full Text] [Related]  

  • 16. Triploid live full-term infant.
    Prats J; Sarret E; Moragas A; Martin C
    Helv Paediatr Acta; 1971 Jun; 26(2):164-72. PubMed ID: 5167785
    [No Abstract]   [Full Text] [Related]  

  • 17. [Structural chromosome abnormality (Gp+) in 2 families with hydrocephalus].
    Walbaum R
    Lille Med; 1969; 14(7):794-8. PubMed ID: 5360846
    [No Abstract]   [Full Text] [Related]  

  • 18. Partial serial duplication of the short arm of chromosome 3.
    Zhang SZ; Wang Q
    Chin Med J (Engl); 1984 Jun; 97(6):425-8. PubMed ID: 6437761
    [No Abstract]   [Full Text] [Related]  

  • 19. [Genetics in eye diseases].
    Keith CG
    Buch Augenarzt; 1981; (83):1-127. PubMed ID: 6784888
    [No Abstract]   [Full Text] [Related]  

  • 20. [Chromosome aberrations and child psychiatry].
    de Grouchy J
    Ann Med Psychol (Paris); 1966 Jun; 124(1):105-6. PubMed ID: 5941447
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 9.