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 *

127 related articles for article (PubMed ID: 881719)

  • 1. Prenatal recognition of 4p- syndrome.
    Blunt S; Berry AC; Seller MJ; Williams CA
    J Med Genet; 1977 Jun; 14(3):232-3. PubMed ID: 881719
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. Chromosome instability limited to the aneuploid clone in the Pallister-Killian syndrome: a pitfall in prenatal diagnosis.
    Zollino M; Bajer J; Neri G
    Prenat Diagn; 1999 Feb; 19(2):184-5. PubMed ID: 10215084
    [No Abstract]   [Full Text] [Related]  

  • 4. 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]  

  • 5. Interstitial deletion of the short arm of chromosome 4.
    Ray M; Evans J; Rockman-Greenberg C; Wickstrom D
    J Med Genet; 1984 Jun; 21(3):223-5. PubMed ID: 6748021
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. 4p- syndrome in a girl with translocation t(1;4)(q11;p16)mat.
    Stoll C; Pennerath A; Lausecker C
    Hum Genet; 1981; 56(3):413-5. PubMed ID: 7239524
    [No Abstract]   [Full Text] [Related]  

  • 8. [Syndrome 4p-].
    Subrt I; Blehová B
    Cesk Pediatr; 1973 Feb; 28(2):75-7. PubMed ID: 4686581
    [No Abstract]   [Full Text] [Related]  

  • 9. Partial deletion of short arm of chromosome no. 4.
    Mace JW; Cunningham MD; Miller OJ; Breg WR
    J Pediatr; 1971 May; 78(5):911-2. PubMed ID: 5581598
    [No Abstract]   [Full Text] [Related]  

  • 10. New autosomal syndromes: trisomies 4p and 9p.
    Dallapiccola B; Mastroiacovo P; Segni G
    Acta Genet Med Gemellol (Roma); 1977; 26(3-4):267-73. PubMed ID: 613692
    [No Abstract]   [Full Text] [Related]  

  • 11. [Early diagnosis of the trisomy 15q proximialis syndrome].
    Tsancheva MS; Lalov VM; Krachunova MG
    Pediatriia; 1982 Jan; (1):65-6. PubMed ID: 7063327
    [No Abstract]   [Full Text] [Related]  

  • 12. 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]  

  • 13. 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]  

  • 14. Inv dup(15) supernumerary marker chromosomes.
    Webb T
    J Med Genet; 1994 Aug; 31(8):585-94. PubMed ID: 7815414
    [No Abstract]   [Full Text] [Related]  

  • 15. 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]  

  • 16. [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]  

  • 17. [A new clinico-cytogenetic syndrome--a proximal deletion of the short arm of chromosome 17].
    Zaletaev DV; Marincheva GS
    Pediatriia; 1988; (11):82-4. PubMed ID: 3226810
    [No Abstract]   [Full Text] [Related]  

  • 18. [Ring of the chromosome 4. I - With 4p- phenotype].
    Fraisse J; Lauras B; Couturier J; Freycon F
    Ann Genet; 1977 Jun; 20(2):101-4. PubMed ID: 302681
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Trisomy 9 mosaicism with multiple congenital anomalies.
    Haslam RH; Broske SP; Moore CM; Thomas GH; Neill CA
    J Med Genet; 1973 Jun; 10(2):180-4. PubMed ID: 4714587
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Prenatal diagnosis of smith-magenis syndrome (del 17p11.2).
    Thomas DG; Jacques SM; Flore LA; Feldman B; Evans MI; Qureshi F
    Fetal Diagn Ther; 2000; 15(6):335-7. PubMed ID: 11111213
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.