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 *

97 related articles for article (PubMed ID: 2363438)

  • 1. Distal 12p deletion in a stillborn infant.
    Baroncini A; Avellini C; Neri C; Forabosco A
    Am J Med Genet; 1990 Jul; 36(3):358-60. PubMed ID: 2363438
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Two patients with chromosome 6q terminal deletions with breakpoints at q24.3 and q25.3.
    Meng J; Fujita H; Nagahara N; Kashiwai A; Yoshioka Y; Funato M
    Am J Med Genet; 1992 Jul; 43(4):747-50. PubMed ID: 1621768
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Phenotypic variation in the del(12p) syndrome.
    Kivlin JD; Fineman RM; Williams MS
    Am J Med Genet; 1985 Dec; 22(4):769-79. PubMed ID: 4073126
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A case of interstitial 1q deletion [46,XY,del(q25q32.1)].
    Hamano S; Fukushima Y; Yamada T; Shimizu H; Okuyama M; Ito F; Maekawa K
    Ann Genet; 1987; 30(2):105-8. PubMed ID: 3314663
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Intercalary de novo deletion of chromosome 1: del(1) (q24 to q32)].
    Faugeras C; Barthe D
    J Genet Hum; 1985 Jan; 33(1):51-6. PubMed ID: 3981142
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A specific syndrome due to deletion of the distal long arm of chromosome 1.
    Meinecke P; Vögtel D
    Am J Med Genet; 1987 Oct; 28(2):371-6. PubMed ID: 3322005
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Del(1)(q22-q25) syndrome. Cytogenetics and phenotype].
    Zaletaev DV; Dadali EL; Kuleshov NP
    Tsitol Genet; 1987; 21(3):213-6. PubMed ID: 3617217
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Cytogenetic and molecular analysis in trisomy 12p.
    Allen TL; Brothman AR; Carey JC; Chance PF
    Am J Med Genet; 1996 May; 63(1):250-6. PubMed ID: 8723118
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Deletion 2q37: an identifiable clinical syndrome with mental retardation and autism.
    Galasso C; Lo-Castro A; Lalli C; Nardone AM; Gullotta F; Curatolo P
    J Child Neurol; 2008 Jul; 23(7):802-6. PubMed ID: 18658079
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Brief cytogenetic case report: a 4.5-year-old girl with deletion 4q syndrome--de novo, 46,XX, del(4) (pter leads to q31:).
    Young RS; Palmer CG; Bender HA; Weaver DD; Hodes ME
    Am J Med Genet; 1982 May; 12(1):103-7. PubMed ID: 7091193
    [No Abstract]   [Full Text] [Related]  

  • 11. A case of de novo trisomy 12p syndrome.
    Ray M; Chudley AE; Christie N; Seargeant L
    Ann Genet; 1985; 28(4):235-8. PubMed ID: 3879436
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. 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]  

  • 14. 4p- syndrome and 9p tetrasomy mosaicism with cleft lip and palate.
    Kobayashi J; Kimijima Y; Yamada S; Amagasa T; Saito-Ohara F
    J Craniomaxillofac Surg; 2000 Jun; 28(3):165-70. PubMed ID: 10964553
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Brief clinical report: interstitial deletion of the long arm of chromosome 4, del(4)(q28-->q31.3).
    Copelli S; del Rey G; Heinrich J; Coco R
    Am J Med Genet; 1995 Jan; 55(1):77-9. PubMed ID: 7702102
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Interstitial deletions of the short arm of chromosome 4 in patients with a similar combination of multiple minor anomalies and mental retardation.
    White DM; Pillers DA; Reiss JA; Brown MG; Magenis RE
    Am J Med Genet; 1995 Jul; 57(4):588-97. PubMed ID: 7573135
    [TBL] [Abstract][Full Text] [Related]  

  • 17. De novo del(3)(q2800).
    Alvarez Arratia MC; Rivera H; Möller M; Valdivia A; Vigueras A; Cantu JM
    Ann Genet; 1984; 27(2):109-11. PubMed ID: 6331786
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Clinical and molecular cytogenetic observations in three cases of "trisomy 12p syndrome".
    Rauch A; Trautmann U; Pfeiffer RA
    Am J Med Genet; 1996 May; 63(1):243-9. PubMed ID: 8723117
    [TBL] [Abstract][Full Text] [Related]  

  • 19. De novo 18q deletion with mitral valve insufficiency.
    Gunes S; Okten G; Kara N; Saglam Y; Tasdemir HA; Kayacik OE; Tural S
    Genet Couns; 2008; 19(3):261-5. PubMed ID: 18990980
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Interstitial deletion 13q: further delineation of the syndrome by clinical and high-resolution chromosome analysis of five patients.
    Tranebjaerg L; Nielsen KB; Tommerup N; Warburg M; Mikkelsen M
    Am J Med Genet; 1988 Apr; 29(4):739-53. PubMed ID: 3400720
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 5.