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 *

59 related articles for article (PubMed ID: 1203470)

  • 1. Gene mapping by exclusion.
    Ferguson-Smith MA
    Birth Defects Orig Artic Ser; 1975; 11(3):126-9. PubMed ID: 1203470
    [No Abstract]   [Full Text] [Related]  

  • 2. Gene mapping by exclusion: the current status.
    Aitken DA; Ferguson-Smith MA; Dick HM
    Birth Defects Orig Artic Ser; 1976; 12(7):256-65. PubMed ID: 1024621
    [No Abstract]   [Full Text] [Related]  

  • 3. Gene mapping by exclusion.
    Ferguson-Smith MA
    Cytogenet Cell Genet; 1975; 14(3-6):296-9. PubMed ID: 1192806
    [No Abstract]   [Full Text] [Related]  

  • 4. Elusive chromosome anomalies.
    Francke U
    Hosp Pract (Off Ed); 1986 May; 21(5):175-8, 182, 191-3. PubMed ID: 3084511
    [No Abstract]   [Full Text] [Related]  

  • 5. Brief clinical report: ring chromosome 17 in a mentally retarded young man - clinical, cytogenetic, and biochemical investigations.
    Chudley AE; Pabello PD; McAlpine PJ; Nickel BE; Shokeir MH
    Am J Med Genet; 1982 Jun; 12(2):219-25. PubMed ID: 7048927
    [TBL] [Abstract][Full Text] [Related]  

  • 6. An International System for Human Cytogenetic Nomenclature (1985) ISCN 1985. Report of the Standing Committee on Human Cytogenetic Nomenclature.
    Birth Defects Orig Artic Ser; 1985; 21(1):1-117. PubMed ID: 4041569
    [No Abstract]   [Full Text] [Related]  

  • 7. Neuroblastoma in a boy with MCA/MR syndrome, deletion 11q, and duplication 12q.
    Koiffmann CP; Gonzalez CH; Vianna-Morgante AM; Kim CA; Odone-Filho V; Wajntal A
    Am J Med Genet; 1995 Jul; 58(1):46-9. PubMed ID: 7573155
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Deletion mapping of the human X chromosome.
    de la Chapelle A; Schröder J; Haahtela T; Aro P
    Hereditas; 1975; 80(1):113-20. PubMed ID: 1141012
    [No Abstract]   [Full Text] [Related]  

  • 9. 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]  

  • 10. Cytogenetics of parametrial leiomyoma.
    Dahlenfors R; Havel G; Wedell B; Mark J
    Anticancer Res; 1997; 17(3C):2121-2. PubMed ID: 9216674
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Erroneous interpretation of Y-chromosome deletion del (Y)(q11) with infertility as Philadelphia chromosome positive chronic myeloid leukemia].
    Mittermüller J; Düll T; Schmetzer H
    Med Klin (Munich); 1994 May; 89(5):279-82. PubMed ID: 8052184
    [No Abstract]   [Full Text] [Related]  

  • 12. 46,XX,-12,+der(12),rcp(3;12)(p25.1;p13.31)pat karyotype in a girl. Probable subregional assignment of glyceraldehyde-3-phosphate dehydrogenase locus to 12p13.1----p13.31 by exclusion mapping.
    Rivas F; Vaca G; Zúñiga G; González RM; Ruiz C; Rivera H; Moller M; Cantu JM
    Ann Genet; 1985; 28(3):189-92. PubMed ID: 3879156
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Cytogenetic and morphologic characteristics of gastrointestinal stromal tumors. Recurrent rearrangement of chromosome 1 and losses of chromosomes 14 and 22 as common anomalies.
    Bergmann F; Gunawan B; Hermanns B; Höer J; Schumpelick V; Füzesi L
    Verh Dtsch Ges Pathol; 1998; 82():275-8. PubMed ID: 10095446
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Comparative gene mapping and human karyotype evolution].
    Hirai M; Suto Y
    Tanpakushitsu Kakusan Koso; 1996 Nov; 41(15 Suppl):2441-9. PubMed ID: 8952408
    [No Abstract]   [Full Text] [Related]  

  • 15. Duncan Guthrie Institute of Medical Genetics, Glasgow, University of Glasgow, Scotland.
    Ferguson-Smith MA; Aitken DA
    Birth Defects Orig Artic Ser; 1982; 18(2):24-42. PubMed ID: 6760922
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Nonisotopic in situ hybridization. Clinical cytogenetics and gene mapping applications.
    Adinolfi M; Crolla J
    Adv Hum Genet; 1994; 22():187-255. PubMed ID: 7762453
    [No Abstract]   [Full Text] [Related]  

  • 17. [Interstitial deletion of the long arm of chromosome 7 and its clinical correlations].
    Del Porto G; D'Alessandro E; De Matteis C; Lo Re ML; Ivaldi M; Di Fusco C
    Pathologica; 1983; 75 Suppl():268-71. PubMed ID: 6680429
    [No Abstract]   [Full Text] [Related]  

  • 18. [Chromosome diagnosis in leukemia].
    Gebhart E
    Med Klin (Munich); 1988 Nov; 83(22):753-9. PubMed ID: 3070313
    [No Abstract]   [Full Text] [Related]  

  • 19. Fine mapping of re-arranged Y chromosome in three infertile patients with non-obstructive azoospermia/cryptozoospermia.
    Faure AK; Aknin-Seifer I; Satre V; Amblard F; Devillard F; Hennebicq S; Chouteau J; Bergues U; Levy R; Rousseaux S
    Hum Reprod; 2007 Jul; 22(7):1854-60. PubMed ID: 17582144
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [13q syndrome. Deletion of the long arm of chromosome No. 13].
    Andersen EA; Mikkelsen M
    Ugeskr Laeger; 1976 Jan; 138(4):227. PubMed ID: 1251485
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 3.