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 *

84 related articles for article (PubMed ID: 293131)

  • 1. Deletion mapping: further evidence for the location of acid phosphatase (ACP1) within 2p23.
    Emanuel BS; Zackai EH; Van Dyke DC; Swallow DM; Allen FH; Mellman WJ
    Am J Med Genet; 1979; 4(2):167-72. PubMed ID: 293131
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Deletion of 2p: a cytogenetic and clinical update.
    Neidich J; Zackai E; Aronson M; Emanuel BS
    Am J Med Genet; 1987 Jul; 27(3):707-10. PubMed ID: 3477100
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Linkage to Tourette syndrome is excluded for red-cell acid phosphatase (ACP1) and flanking markers on chromosome 2pter-2p23.
    Devor EJ; Henderson V; Sparkes RS
    Hum Biol; 1991 Apr; 63(2):221-6. PubMed ID: 2019415
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Interstitial deletion of chromosome 2 (p23p25).
    Penchaszadeh VB; Dowling PK; Davis JG; Schmidt R; Wapnir RA
    Am J Med Genet; 1987 Jul; 27(3):701-6. PubMed ID: 3477099
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Duplication of 2p25: confirmation of the assignment of soluble acid phosphatase (ACP1) locus to 2p25.
    Wakita Y; Narahara K; Takahashi Y; Kikkawa K; Kimura S; Oda M; Kimoto H
    Hum Genet; 1985; 71(3):259-60. PubMed ID: 4065897
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Physical findings in 21q22 deletion suggest critical region for 21q- phenotype in q22.
    Theodoropoulos DS; Cowan JM; Elias ER; Cole C
    Am J Med Genet; 1995 Nov; 59(2):161-3. PubMed ID: 8588579
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Partial duplication for the short arm of chromosome 2 : the 2p23 to pter syndrome.
    Rosenfeld W; Verma RS; Jhaveri R; Dosik H; Evans H
    Ann Genet; 1982; 25(1):28-31. PubMed ID: 6979296
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Further evidence for the assignment of the red cell acid phosphatase gene (ACP1) to the short arm of chromosome 2 from gene dosage effect.
    Magenis RE; Koler RD; Lovrien E; Bigley RH; DuVal MC; Overton KM
    Birth Defects Orig Artic Ser; 1976; 12(7):326-7. PubMed ID: 1024633
    [No Abstract]   [Full Text] [Related]  

  • 9. Further evidence by gene dosage for the regional assignment of erythrocyte acid phosphatase (ACP1) and malate dehydrogenase (MDH1) loci on chromosome 2p.
    Larson LM; Bruce AW; Saumur JH; Wasdahl WA
    Clin Genet; 1982 Oct; 22(4):220-5. PubMed ID: 7151307
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Clinical and cytogenetic findings in seven cases of inverted duplication of 8p with evidence of a telomeric deletion using fluorescence in situ hybridization.
    Guo WJ; Callif-Daley F; Zapata MC; Miller ME
    Am J Med Genet; 1995 Sep; 58(3):230-6. PubMed ID: 8533823
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Interstitial deletion of chromosome 3p: report of a patient and delineation of a proximal 3p deletion syndrome.
    Neri G; Reynolds JF; Westphal J; Hinz J; Daniel A
    Am J Med Genet; 1984 Sep; 19(1):189-93. PubMed ID: 6496569
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Regional assignment of red cell acid phosphatase locus to band 2p25.
    Junien C; Kaplan JC; Bernheim A; Berger R
    Hum Genet; 1979 Apr; 48(1):17-21. PubMed ID: 457131
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Subtle overlapping deletions in the terminal region of chromosome 6q24.2-q26: three cases studied using FISH.
    Sukumar S; Wang S; Hoang K; Vanchiere CM; England K; Fick R; Pagon B; Reddy KS
    Am J Med Genet; 1999 Nov; 87(1):17-22. PubMed ID: 10528241
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Refined genotype-phenotype correlations in cases of chromosome 6p deletion syndromes.
    Mirza G; Williams RR; Mohammed S; Clark R; Newbury-Ecob R; Baldinger S; Flinter F; Ragoussis J
    Eur J Hum Genet; 2004 Sep; 12(9):718-28. PubMed ID: 15150541
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Terminal deletion of 6p: report of a new case.
    Plaja A; Vidal R; Soriano D; Bou X; Vendrell T; Mediano C; Pueyo JM; Labraña X; Sarret E
    Ann Genet; 1994; 37(4):196-9. PubMed ID: 7710255
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Distal 11q deletion: a specific clinical entity.
    Fryns JP; Kleczkowska A; Smeets E; Van den Berghe H
    Helv Paediatr Acta; 1987 Oct; 42(2-3):191-4. PubMed ID: 3692885
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A new case of interstitial deletion of chromosome 3q, del(3q)(q13.12q21.3), with agenesis of the corpus callosum.
    Genuardi M; Calvieri F; Tozzi C; Coslovi R; Neri G
    Clin Dysmorphol; 1994 Oct; 3(4):292-6. PubMed ID: 7894733
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Chromosome 7p--syndrome: craniosynostosis with preservation of region 7p2.
    Aughton DJ; Cassidy SB; Whiteman DA; Delach JA; Guttmacher AE
    Am J Med Genet; 1991 Sep; 40(4):440-3. PubMed ID: 1746608
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Two patients with interstitial del (14q), one with features of Holt-Oram syndrome. Exclusion mapping of PI (alpha-1-antitrypsin).
    Turleau C; de Grouchy J; Chavin-Colin F; Dore F; Seger J; Dautzenberg MD; Arthuis M; Jeanson C
    Ann Genet; 1984; 27(4):237-40. PubMed ID: 6335371
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Further evidence for the assignment of the red cell acid phosphatase gene (ACP1) to the short arm of chromosome 2 from gene dosage effect.
    Magenis RE; Koler RD; Lovrien E; Bigley RH; DuVal MC; Overton KM
    Cytogenet Cell Genet; 1976; 16(1-5):326-7. PubMed ID: 975901
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 5.