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 *

98 related articles for article (PubMed ID: 315197)

  • 21. Delineation of a characteristic phenotype in distal trisomy 2q.
    Kyllerman M; Wahlström J; Westerberg B; Gustavson KH
    Helv Paediatr Acta; 1984 Dec; 39(5-6):499-508. PubMed ID: 6543860
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Loss of the N-myc oncogene in a patient with a small interstitial deletion of the short arm of chromosome 2.
    Saal HM; King LJ; Zimmerman D; Johnson RC; Carr AG; Samango-Sprouse CA; Stanley W
    Am J Med Genet; 1996 Dec; 66(4):373-7. PubMed ID: 8989454
    [TBL] [Abstract][Full Text] [Related]  

  • 23. 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]  

  • 24. [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]  

  • 25. A new syndrome of proximal deletion of the long arm of chromosome 1: 1q21-23 leads to 1q25.
    Taysi K; Sekhon GS; Hillman RE
    Am J Med Genet; 1982 Dec; 13(4):423-30. PubMed ID: 7158642
    [No Abstract]   [Full Text] [Related]  

  • 26. An epileptic case with mosaic ring chromosome 6 and 6q terminal deletion.
    Kara N; Okten G; Guneş SO; Saglam Y; Tasdemir HA; Pinarli FA
    Epilepsy Res; 2008 Aug; 80(2-3):219-23. PubMed ID: 18485670
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Infant with multiple congenital anomalies and deletion (9)(q34.3).
    Schimmenti LA; Berry SA; Tuchman M; Hirsch B
    Am J Med Genet; 1994 Jun; 51(2):140-2. PubMed ID: 7522397
    [TBL] [Abstract][Full Text] [Related]  

  • 28. 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]  

  • 29. De novo deletion of chromosome 9 (9p-) in a child with multiple congenital anomalies and psychomotor retardation.
    Murthy DS; Murthy SK; Banker GJ; Patel AJ
    Indian Pediatr; 1991 May; 28(5):546-9. PubMed ID: 1684352
    [No Abstract]   [Full Text] [Related]  

  • 30. 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]  

  • 31. Deletion of the distal long arm of chromosome 1: a definable syndrome.
    Johnson VP; Heck LJ; Carter GA; Flom JO
    Am J Med Genet; 1985 Dec; 22(4):685-94. PubMed ID: 4073121
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Phenotype associated with ring 10 chromosome: report of patient and review of literature.
    Michels VV; Driscoll DJ; Ledbetter DH; Riccardi VM
    Am J Med Genet; 1981; 9(3):231-7. PubMed ID: 7025632
    [TBL] [Abstract][Full Text] [Related]  

  • 33. De novo interstitial deletion q16.2q21 on chromosome 6.
    Villa A; Urioste M; Bofarull JM; Martínez-Frías ML
    Am J Med Genet; 1995 Jan; 55(3):379-83. PubMed ID: 7726240
    [TBL] [Abstract][Full Text] [Related]  

  • 34. De novo satellited 21q associated with corpus callosum dysgenesis, colpocephaly, a concealed penis, congenital heart defects, and developmental delay.
    Chen CP; Lin SP; Chern SR; Lee CC; Huang JK; Wang W; Liao YW
    Genet Couns; 2004; 15(4):437-42. PubMed ID: 15658619
    [TBL] [Abstract][Full Text] [Related]  

  • 35. 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]  

  • 36. Interstitial deletion of the long arm of chromosome 6.
    Chery M; Formiga LF; Mujica P; André M; Stehelin D; Dozier C; Gilgenkrantz S
    Ann Genet; 1989; 32(2):82-6. PubMed ID: 2757364
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Terminal deletion 4q in a severely retarded boy.
    de Michelena MI; Campos PJ
    Am J Med Genet; 1989 Jun; 33(2):228-30. PubMed ID: 2764033
    [TBL] [Abstract][Full Text] [Related]  

  • 38. 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]  

  • 39. Interstitial deletion of the long arm of chromosome 1 [del(1)(q32q42)].
    Al-Awadi SA; Farag TI; Usha R; el-Khalifa MY; Sundareshan TS; Al-Othman SA
    Am J Med Genet; 1986 Apr; 23(4):931-3. PubMed ID: 3963055
    [TBL] [Abstract][Full Text] [Related]  

  • 40. 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]  

    [Previous]   [Next]    [New Search]
    of 5.