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 *

140 related articles for article (PubMed ID: 5494356)

  • 1. [Free trisomy concerning a little acrocentric chromosome in a non-mongoloid female patient. Trisomy 22 or partial trisomy D?].
    Malpuech G; Menut G; Raynaud EJ; Lavignon A
    Pediatrie; 1970 Dec; 25(8):901-10. PubMed ID: 5494356
    [No Abstract]   [Full Text] [Related]  

  • 2. [Multiple malformations in partial trisomy C (12) as manifestation of an inherited E-C (18/12) translocation].
    Bühler UK; Bühler EM; Sartorius J; Stalder GR
    Helv Paediatr Acta; 1967 Apr; 22(1):41-53. PubMed ID: 5585048
    [No Abstract]   [Full Text] [Related]  

  • 3. Familial D/D and D/G, translocation.
    Orye E; Delire C
    Helv Paediatr Acta; 1967 Apr; 22(1):36-40. PubMed ID: 4230976
    [No Abstract]   [Full Text] [Related]  

  • 4. [Congenital leukemia with chromosome aberrations (Trisomy G) in a non-mongoloid child].
    Bjönness H; Bühler EM; Fricker H; Gugler E
    Helv Paediatr Acta; 1974 Nov; 29(5):457-70. PubMed ID: 4281418
    [No Abstract]   [Full Text] [Related]  

  • 5. [Prenatal diagnosis of a de novo trisomy case 9q-47,XX,+9 del(q33----qter)].
    Cordier MP; Coicaud C; Thoulon JM; Robert JM; Germain D
    J Genet Hum; 1984 Dec; 32(5):351-61. PubMed ID: 6527131
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [D 1 trisomy and its cytogenetic and clinical differences--report of 3 cases].
    Zergollern L; Hitrec V; Stampar B; Gorecan V
    Acta Med Iugosl; 1971; 25(2):157-73. PubMed ID: 5119679
    [No Abstract]   [Full Text] [Related]  

  • 7. Precarious acrocentric short arm in prenatal diagnosis: no chromosome 14 polymorphism, but trisomy 17p.
    De Pater JM; Van Tintelen JP; Stigter R; Brouwers HA; Scheres JM
    Genet Couns; 2000; 11(3):241-7. PubMed ID: 11043432
    [TBL] [Abstract][Full Text] [Related]  

  • 8. The prenatal diagnosis of chromosome anomalies.
    Schmid W
    Triangle; 1972; 11(3):91-102. PubMed ID: 4656755
    [No Abstract]   [Full Text] [Related]  

  • 9. Prenatal diagnosis of partial trisomy 1q using fluorescent in situ hybridization.
    DuPont BR; Huff RW; Ridgway LE; Stratton RF; Moore CM
    Am J Med Genet; 1994 Mar; 50(1):21-7. PubMed ID: 8160748
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Chromosome abnormalities and child psychiatry].
    de Grouchy J
    Rev Neuropsychiatr Infant; 1967; 15(4):263-73. PubMed ID: 5602320
    [No Abstract]   [Full Text] [Related]  

  • 11. [Trisomy of group C (47, XX, C+)].
    Emberger JM; Rey J; Rieu D; Dossa D; Bonnet H; Jean R
    Arch Fr Pediatr; 1970; 27(10):1081-8. PubMed ID: 5495708
    [No Abstract]   [Full Text] [Related]  

  • 12. [Trisomy 10p as a result of familial 10/22 translocation].
    Zergollern L; Begovic D; Muzinić D
    Acta Med Iugosl; 1980; 34(2):113-22. PubMed ID: 7405617
    [No Abstract]   [Full Text] [Related]  

  • 13. [A new case of partial trisomy 8p].
    Gemme G; Bonioli E; Lagorio V; Bellini C; Caledoni S; Vianello MG
    Minerva Pediatr; 1981 Dec; 33(24):1211-4. PubMed ID: 7038428
    [No Abstract]   [Full Text] [Related]  

  • 14. [Late prenatal diagnosis of fetal growth retardation: the diagnosis of a case of trisomy 18 (author's transl)].
    Le Marec B; Defawe G; Mention JE; Picard F; Duval JM; Dubois J
    J Gynecol Obstet Biol Reprod (Paris); 1980; 9(6):655-7. PubMed ID: 7462570
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Trisomy 18 (Edwards syndrome) in Delaware.
    Morallo LM; Rosenblum H; Esterly KL; Johnson WD; Storlazzi JJ; Narvaez AC; Borgaonkar DS
    Del Med J; 1983 Jan; 55(1):27-30. PubMed ID: 6840358
    [No Abstract]   [Full Text] [Related]  

  • 16. [Trisomy 10 p. Apropos of a case caused by a maternal translocation].
    Stoll C; Willard D
    Pediatrie; 1980; 35(3):251-5. PubMed ID: 7393692
    [No Abstract]   [Full Text] [Related]  

  • 17. [Prenatal diagnosis of te Dandy-Walker syndrome associated with partial trisomy of chromosome 9].
    Zacharias S; Nazer J; Lacassie I; Ibarra A; Valencia JM
    Rev Chil Obstet Ginecol; 1983; 48(6):414-8. PubMed ID: 6681216
    [No Abstract]   [Full Text] [Related]  

  • 18. Trisomy 18-Edwards syndrome: a report of three patients.
    Ejiwumni AB; Msamati BC
    Cent Afr J Med; 1993 May; 39(5):105-9. PubMed ID: 8131193
    [No Abstract]   [Full Text] [Related]  

  • 19. Prenatal diagnosis of a 5/15 translocation with 5p and proximal 5q trisomy. Cytogenetic and phenotypic findings.
    Crowder WE; Yeast JD; Falk RE
    Birth Defects Orig Artic Ser; 1982; 18(3 Pt A):143-51. PubMed ID: 7126787
    [No Abstract]   [Full Text] [Related]  

  • 20. [Diagnosis and prevention of chromosome aberrations].
    Sachs ES; van Hemel JO
    Ned Tijdschr Geneeskd; 1982 Dec; 126(49):2236-44. PubMed ID: 6217426
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 7.