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 *

130 related articles for article (PubMed ID: 8111185)

  • 1. Silver-like syndrome and a small deletion on chromosome 13.
    Wahlström J; Holmgren G; Albertsson-Wikland K; Törnhage CJ
    Acta Paediatr; 1993 Nov; 82(11):993-6. PubMed ID: 8111185
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Developmental delay and dysmorphic features associated with a previously undescribed deletion on chromosome 1.
    Barton JS; O'Loughlin J; Howell RT; L'e Orme R
    J Med Genet; 1995 Aug; 32(8):636-7. PubMed ID: 7473657
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Loss of the 3p25.3 band is critical in the manifestation of del(3p) syndrome: karyotype-phenotype correlation in cases with deficiency of the distal portion of the short arm of chromosome 3.
    Narahara K; Kikkawa K; Murakami M; Hiramoto K; Namba H; Tsuji K; Yokoyama Y; Kimoto H
    Am J Med Genet; 1990 Feb; 35(2):269-73. PubMed ID: 2178418
    [TBL] [Abstract][Full Text] [Related]  

  • 4. The phenotype of ring chromosome 3.
    Wilson GN; Pooley J; Parker J
    J Med Genet; 1982 Dec; 19(6):471-3. PubMed ID: 7154048
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Distinct 15q genotypes in Russell-Silver and ring 15 syndromes.
    Rogan PK; Seip JR; Driscoll DJ; Papenhausen PR; Johnson VP; Raskin S; Woodward AL; Butler MG
    Am J Med Genet; 1996 Mar; 62(1):10-5. PubMed ID: 8779316
    [TBL] [Abstract][Full Text] [Related]  

  • 6. The 8p- syndrome.
    Reiss JA; Brenes PM; Chamberlin J; Magenis RE; Lovrien EW
    Hum Genet; 1979 Mar; 47(2):135-40. PubMed ID: 437781
    [TBL] [Abstract][Full Text] [Related]  

  • 7. The 18p- syndrome. Report of five cases.
    Zumel RM; Darnaude MT; Delicado A; Diaz de Bustamante A; de Torres ML; López-Pájares I
    Ann Genet; 1989; 32(3):160-3. PubMed ID: 2817777
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Inherited parital duplication deficiency of chromosome 15 (p12;q22).
    Coco R; Penchaszadeh VB
    J Genet Hum; 1978 Sep; 26(3):203-10. PubMed ID: 739260
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Partial deletion 8q without Langer-Giedion syndrome: a recognisable syndrome.
    Fennell SJ; Benson JW; Kindley AD; Schwarz MJ; Czepulkowski B
    J Med Genet; 1989 Mar; 26(3):167-71. PubMed ID: 2651669
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Deletion of long arms of chromosome 13.
    Kucerovă M; Polívková Z; Pokorná M
    Humangenetik; 1975; 27(3):255-7. PubMed ID: 1150247
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [De novo partial monosomy 10p].
    Ibáñez Micó S; Solaz Barrios S; Aleu Pérez-Gramunt M; García Vicent C
    An Pediatr (Barc); 2006 Dec; 65(6):627-8. PubMed ID: 17194334
    [No Abstract]   [Full Text] [Related]  

  • 12. 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]  

  • 13. [Monosomy 7qter (author's transl)].
    Turleau C; de Grouchy J; Perignon F; Lenoir G
    Ann Genet; 1979; 22(4):242-4. PubMed ID: 317790
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Direct transmission of the 18q- syndrome from mother to daughter.
    Chen CP; Lin SP; Chern SR; Lee CC; Huang JK; Wang W
    Genet Couns; 2006; 17(2):185-9. PubMed ID: 16970036
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Phenotypic delineation of ring chromosome 15 and Russell-Silver syndromes.
    Wilson GN; Sauder SE; Bush M; Beitins IZ
    J Med Genet; 1985 Jun; 22(3):233-6. PubMed ID: 4040173
    [TBL] [Abstract][Full Text] [Related]  

  • 16. De novo interstitial deletion of the long arm of chromosome 3: 46,XX,del(3)(q25.1q26.1).
    Robin NH; Magnusson M; McDonald-McGinn D; Zackai EH; Spinner NB
    Clin Genet; 1993 Dec; 44(6):335-7. PubMed ID: 8131307
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 46,XX/46,XX,del(20)(pter-->p12.2) mosaicism limited to fibroblasts associated with MCA/MR and severe growth deficit.
    Fryns JP; Kleczkowska A; Decock P; Massa G; van den Berghe H
    Ann Genet; 1992; 35(4):234-6. PubMed ID: 1296522
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Syndromes associated with deletion of the long arm of chromosome 18[del(18q)].
    Wilson MG; Towner JW; Forsman I; Siris E
    Am J Med Genet; 1979; 3(2):155-74. PubMed ID: 474629
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Terminal deletion of the long arm of chromosome 2 in a mildly dysmorphic hypotonic infant with karyotype 46,XY,del(2)(q37).
    Gorski JL; Cox BA; Kyine M; Uhlmann W; Glover TW
    Am J Med Genet; 1989 Mar; 32(3):350-2. PubMed ID: 2729355
    [TBL] [Abstract][Full Text] [Related]  

  • 20. The syndrome of ring chromosome 12.
    Scribanu N; McCullars EB; Baumiller RC; Colon AR
    Am J Med Genet; 1980; 5(2):165-70. PubMed ID: 7395909
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.