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 *

147 related articles for article (PubMed ID: 5449950)

  • 1. Human chromosomal deficiency: the 4p--syndrome.
    Passarge E; Altrogge HC; Rüdiger RA
    Humangenetik; 1970 Aug; 10(1):51-7. PubMed ID: 5449950
    [No Abstract]   [Full Text] [Related]  

  • 2. Partial deletion of the short arm of chromosome no. 4(4p-): clinical studies in five unrelated patients.
    Miller OJ; Breg WR; Warburton D; Miller DA; DeCapoa A; Allderdice PW; Davis J; Klinger HP; McGilvray E; Allen FH
    J Pediatr; 1970 Nov; 77(5):792-801. PubMed ID: 5504070
    [No Abstract]   [Full Text] [Related]  

  • 3. Holt-Oram syndrome associated with ectromelia and chromosomal aberrations.
    Rybak M; Kozlowski K; Kleczkowska A; Lewandowska J; Sokolowski J; Soltysik-Wilk E
    Am J Dis Child; 1971 Jun; 121(6):490-5. PubMed ID: 5581016
    [No Abstract]   [Full Text] [Related]  

  • 4. [Deficiency in the short arms of Group B (4p--; 5p--) chromosomes. Studies on 6 patients].
    Altrogge HC; Hirth L; Goedde HW; Schroeder HJ
    Z Kinderheilkd; 1971; 110(3):218-47. PubMed ID: 5088755
    [No Abstract]   [Full Text] [Related]  

  • 5. [Trisomy 4p due to recombination aneusomy of an inversion 4 (p 14, q 35)].
    Rethoré MO; Dutrillaux B; Job JC; Lejeune J
    Ann Genet; 1974 Jun; 17(2):109-14. PubMed ID: 4547937
    [No Abstract]   [Full Text] [Related]  

  • 6. 4p- phenotype in an infant with t(4p-;19p or q+)mat translocation.
    Neu RL; Shott RJ; Gardner LI
    Am J Dis Child; 1975 Mar; 129(3):363-5. PubMed ID: 1121967
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Translocation 4p-- syndrome: a general review.
    Centerwall WR; Thompson WP; Allen IE; Fobes CD
    Am J Dis Child; 1975 Mar; 129(3):366-70. PubMed ID: 1121968
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. Partial deletion of the short arm of a chromosome No. 4. Wolf's syndrome.
    van Kempen C; Jongbloet PH
    Maandschr Kindergeneeskd; 1967 Oct; 35(8):252-69. PubMed ID: 6065161
    [No Abstract]   [Full Text] [Related]  

  • 10. [Cytogenetic and pathological observations in the (4p-) SYNDROME (Wolf syndrome)].
    Citoler P; Gropp A; Gullotta F
    Beitr Pathol; 1971 Apr; 143(1):84-96. PubMed ID: 5577069
    [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. New syndrome associated with partial deletion of short arms of chromosome No. 4. Clinical manifestations of hypospadias, beaked nose, abnormal iris, hemangioma of forehead, seizures, and other anomalies.
    Leão JC; Bargman GJ; Neu RL; Kajii T; Gardner LI
    JAMA; 1967 Oct; 202(5):434-7. PubMed ID: 6072506
    [No Abstract]   [Full Text] [Related]  

  • 13. Duplication 11 (q21 to 23 leads to qter) syndrome.
    Francke U; Weber F; Sparkes RS; Mattson PD; Mann J
    Birth Defects Orig Artic Ser; 1977; 13(3B):167-86. PubMed ID: 890090
    [No Abstract]   [Full Text] [Related]  

  • 14. 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]  

  • 15. Chromosome abnormalities in two cases with bilateral radial element defects.
    Faed M; Stewart A; Keay AJ
    J Med Genet; 1969 Sep; 6(3):342-6. PubMed ID: 5345108
    [No Abstract]   [Full Text] [Related]  

  • 16. A girl with Wolf-Hirschorn syndrome and mosaicism 46,XX-46,XX,4p-.
    Judge CG; Garson OM; Pitt DB; Sutherland GR
    J Ment Defic Res; 1974 Mar; 18(0):79-85. PubMed ID: 4423845
    [No Abstract]   [Full Text] [Related]  

  • 17. The 4p- syndrome. A clinically recognizable chromosomal deletion syndrome.
    Guthrie RD; Aase JM; Asper AC; Smith DW
    Am J Dis Child; 1971 Nov; 122(5):421-5. PubMed ID: 5129531
    [No Abstract]   [Full Text] [Related]  

  • 18. Ring 13 chromosome associated with microcephaly, congenital heart defect, intrauterine growth retardation, and abnormal skin pigmentation.
    Lowry RB; Dill FJ
    Birth Defects Orig Artic Ser; 1977; 13(3B):216-22. PubMed ID: 890095
    [No Abstract]   [Full Text] [Related]  

  • 19. Cri-du-chat syndrome. Case report.
    Schmid W; Vischer D
    Helv Paediatr Acta; 1967 Apr; 22(1):22-7. PubMed ID: 5585045
    [No Abstract]   [Full Text] [Related]  

  • 20. [Familial translocation t(4;22) (p11;p12) and trisomy 4p in 2 sisters].
    Giovannelli G; Forabosco A; Dutrillaux B
    Ann Genet; 1974 Jun; 17(2):119-24. PubMed ID: 4547939
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 8.