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 *

95 related articles for article (PubMed ID: 862431)

  • 1. Deletion of the short arm of chromosome 2 from a subject with congenital anomalies. Repository identification no. GM-1138.
    Zackai E; Emanuel B; Mellman WJ; Aronson MM; Bozarth B; Greene AE; Coriell LL
    Cytogenet Cell Genet; 1977; 18(2):108. PubMed ID: 862431
    [No Abstract]   [Full Text] [Related]  

  • 2. Interstitial deletion in the long arm of chromosome 1 in a subject with congenital abnormalities. Repository identification No. GM-214.
    de la Chapelle A; Koivisto M; Aronson MM; Greene AE; Coriell LL
    Cytogenet Cell Genet; 1979; 23(3):220. PubMed ID: 436455
    [No Abstract]   [Full Text] [Related]  

  • 3. Duplication of a segment of chromosome 3 in a subject with multiple congenital anomalies and a 47,XYY father, inversion of chromosomes 3 and 9 in the mother, and inversion of chromosome 9 in a brother. Repository identification Nos. GM-1253, GM-1252, and GM-1251.
    Pope IS; Thuline HC; Aronson MM; Bozarth B; Greene AE; Coriell LL
    Cytogenet Cell Genet; 1979; 24(2):127-8. PubMed ID: 477407
    [No Abstract]   [Full Text] [Related]  

  • 4. Deletion in the long arm of chromosome 1 from a subject with multiple congenital anomalies. Respository identification No. GM-2025.
    Sekhon GS; Hillman RE; Yu R; Aronson MM; Greene AE; Coriell LL
    Cytogenet Cell Genet; 1978; 21(3):176. PubMed ID: 657850
    [No Abstract]   [Full Text] [Related]  

  • 5. Deletion in the short arm of chromosome 9 from a subject with congenital cerebral maldevelopment. Repository identification No. GM-870.
    Breg WR; Aronson MM; Hill R; Greene AE; Coriell LL
    Cytogenet Cell Genet; 1976; 17(5):296-7. PubMed ID: 1017321
    [No Abstract]   [Full Text] [Related]  

  • 6. Deletion of the short arm of chromosome 4 from a subject with Wolf's syndrome. Repository identification no. GM-72.
    Breg WR; Aronson MM; Greene AE; Coriell LL
    Cytogenet Cell Genet; 1977; 18(5):307-8. PubMed ID: 560288
    [No Abstract]   [Full Text] [Related]  

  • 7. An unusual ocular finding associated with chromosome 1q deletion syndrome.
    Wright LL; Schwartz MF; Schwartz S; Karesh J
    Pediatrics; 1986 May; 77(5):786. PubMed ID: 3703649
    [No Abstract]   [Full Text] [Related]  

  • 8. Interstitial deletion of the long arm of chromosome no. 7 (7q-) in an infant with multiple anomalies.
    Higginson G; Weaver DD; Magenis RE; Prescott GH; Haag C; Hepburn DJ
    Clin Genet; 1976 Nov; 10(5):307-12. PubMed ID: 991439
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Interstitial deletion of the long arm of chromosome 2: case report and review of literature.
    Taysi K; Dengler DR; Jones LA; Heersma JR
    Ann Genet; 1981; 24(4):245-7. PubMed ID: 7036843
    [No Abstract]   [Full Text] [Related]  

  • 10. A partial long arm deletion of chromosome 7:46,XY,del(7)(q32).
    Kousseff BG; Hsu LY; Paciuc S; Hirschhorn K
    J Med Genet; 1977 Apr; 14(2):144-7. PubMed ID: 192866
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Deletion of the short arm of chromosome No. 10.
    Berger R; Larroche JC; Toubas PL
    Acta Paediatr Scand; 1977 Sep; 66(5):659-62. PubMed ID: 899785
    [No Abstract]   [Full Text] [Related]  

  • 12. Tandem dup (1p) within the short arm of chromosome 1 in a child with ambiguous genitalia and multiple congenital anomalies.
    Elejalde BR; Opitz JM; de Elejalde MM; Gilbert EF; Abellera M; Meisner L; Lebel RR; Hartigan JM
    Am J Med Genet; 1984 Apr; 17(4):723-30. PubMed ID: 6539070
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Deletion of the short arm of chromosome 3: a case report with necropsy findings.
    Beneck D; Suhrland MJ; Dicker R; Greco MA; Wolman SR
    J Med Genet; 1984 Aug; 21(4):307-10. PubMed ID: 6492097
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Partial deletion of the short arm of chromosome 4. Apropos of 3 cases].
    Taillemite JL; Tufferaud G; Hazael-Massieux P; Baheux-Morlier G; Roux C
    Ann Genet; 1977 Jun; 20(2):93-100. PubMed ID: 302690
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [2 new cases of deletion of the short arm of chromosome 9].
    Antonenko VG; Demintseva VS; Demina NA; Levina LIa
    Pediatriia; 1987; (3):81-4. PubMed ID: 3601545
    [No Abstract]   [Full Text] [Related]  

  • 16. A (2;4) translocation, balanced, 46 chromosomes. Repository identification No. GM-1064.
    Biederman B; Bowen P; Aronson MM; Greene AE; Coriell LL
    Cytogenet Cell Genet; 1976; 17(5):300-1. PubMed ID: 1017323
    [No Abstract]   [Full Text] [Related]  

  • 17. Interstitial 3p deletion in a child due to paternal paracentric inserted inversion.
    Wyandt HE; Kasprzak R; Ennis J; Willson K; Koch V; Schnatterly P; Wilson W; Kelly TE
    Am J Hum Genet; 1980 Sep; 32(5):731-5. PubMed ID: 7424912
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Multiple congenital anomalies/mental retardation (MCA/MR) syndrome due to interstitial deletion 1q.
    Steinbach P; Wolf M; Schmidt H
    Am J Med Genet; 1984 Sep; 19(1):131-6. PubMed ID: 6496565
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A (2;4) translocation, unbalanced, 46 chromosomes. Repository identification No. GM-501.
    Biederman B; Bowen P; Aronson MM; Greene AE; Coriell LL
    Cytogenet Cell Genet; 1976; 17(5):298-9. PubMed ID: 1017322
    [No Abstract]   [Full Text] [Related]  

  • 20. Use of fluorescence in situ hybridization to clarify a complex chromosomal rearrangement in a child with multiple congenital anomalies.
    Spikes AS; Hegmann K; Smith JL; Shaffer LG
    Am J Med Genet; 1995 May; 57(1):31-4. PubMed ID: 7645595
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 5.