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 *

99 related articles for article (PubMed ID: 11851277)

  • 21. [DiGeorge syndrome. Velocardiofacial syndrome/chromosome 22q11 deletion syndrome].
    Hoffmann MH; Vadstrup S
    Ugeskr Laeger; 2000 May; 162(19):2736-9. PubMed ID: 10827540
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Diagnosing genetic anomalies by inspection.
    Guthrie E; Mast J; Engel M
    Child Adolesc Psychiatr Clin N Am; 1999 Oct; 8(4):777-90. PubMed ID: 10553203
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Antenatal monitoring of genetic disorders.
    Simpson JL
    Clin Obstet Gynaecol; 1979 Aug; 6(2):259-93. PubMed ID: 387326
    [No Abstract]   [Full Text] [Related]  

  • 24. Is the autosomal dominant Optiz GBBB syndrome part of the DiGeorge/velocardiofacial syndrome with deletions of chromosome area 22q11.2?
    Wulfsberg EA
    Am J Med Genet; 1996 Aug; 64(3):523-4. PubMed ID: 8862634
    [No Abstract]   [Full Text] [Related]  

  • 25. [Transient neonatal hypocalcemia. Onset Manifestation of the 22q11.2 deletion syndrome].
    Pusceddu M; Bertone A; Campra D; Pontoriero D; Guala A
    Minerva Pediatr; 2002 Aug; 54(4):343-5. PubMed ID: 12131871
    [No Abstract]   [Full Text] [Related]  

  • 26. Fetal cells in maternal blood.
    Shulman LP
    Curr Womens Health Rep; 2003 Feb; 3(1):47-54. PubMed ID: 12521552
    [TBL] [Abstract][Full Text] [Related]  

  • 27. [Ethics and genetic diagnosis].
    Bondolfi A
    Schweiz Med Wochenschr; 2000 Nov; 130(44):1662-8. PubMed ID: 11103437
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Is 47 XXY the genetic marker for Aicardi syndrome?
    Saddichha S
    J Child Neurol; 2009 Dec; 24(12):1579; author reply 1579-80. PubMed ID: 19955350
    [No Abstract]   [Full Text] [Related]  

  • 29. Prenatal diagnosis of DiGeorge syndrome.
    Göktolga U; Gezginç K; Ceyhan ST; Fidan U; Ergün A; Bahçe M; Başer I
    Taiwan J Obstet Gynecol; 2008 Dec; 47(4):441-2. PubMed ID: 19126513
    [No Abstract]   [Full Text] [Related]  

  • 30. [Methods of research on the chromosome level in diagnosing genetic disorders].
    Ruffini E
    Minerva Pediatr; 1989 Sep; 41(9):491-2. PubMed ID: 2586382
    [No Abstract]   [Full Text] [Related]  

  • 31. Ascertainment of genetic disease in relatives of affected persons.
    McKusick VA
    Isr J Med Sci; 1973; 9(9):1358-60. PubMed ID: 4775118
    [No Abstract]   [Full Text] [Related]  

  • 32. [Use of DNA polymorphism in the diagnosis of human genetic diseases].
    Cebrat S
    Postepy Hig Med Dosw; 1988; 42(5):461-82. PubMed ID: 2908211
    [No Abstract]   [Full Text] [Related]  

  • 33. "Genetic for medical practitioners".
    Ambani LM
    Q Med Rev; 1981 Oct; 32(4):1-43. PubMed ID: 7051087
    [No Abstract]   [Full Text] [Related]  

  • 34. Dual-probe fluorescence in situ hybridization assay for detecting deletions associated with VCFS/DiGeorge syndrome I and DiGeorge syndrome II loci.
    Berend SA; Spikes AS; Kashork CD; Wu JM; Daw SC; Scambler PJ; Shaffer LG
    Am J Med Genet; 2000 Apr; 91(4):313-7. PubMed ID: 10766989
    [TBL] [Abstract][Full Text] [Related]  

  • 35. First-trimester screening for chromosomal abnormalities: advantages of an instant results approach.
    Norton ME
    Clin Lab Med; 2010 Sep; 30(3):565-71. PubMed ID: 20638572
    [TBL] [Abstract][Full Text] [Related]  

  • 36. [Congenital ocular abnormalities].
    Vérin P; Comte P
    Annee Ther Clin Ophtalmol; 1986; 37():151-78. PubMed ID: 3118764
    [No Abstract]   [Full Text] [Related]  

  • 37. Personal genomics: his daughter's DNA.
    Maher B
    Nature; 2007 Oct; 449(7164):773-6. PubMed ID: 17968422
    [No Abstract]   [Full Text] [Related]  

  • 38. Oversight of genetic testing: an update.
    Kaul KL; Leonard DG; Gonzalez A; Garrett CT
    J Mol Diagn; 2001 Aug; 3(3):85-91. PubMed ID: 11486046
    [No Abstract]   [Full Text] [Related]  

  • 39. DiGeorge anomaly in the absence of chromosome 22q11.2 deletion.
    Rope AF; Cragun DL; Saal HM; Hopkin RJ
    J Pediatr; 2009 Oct; 155(4):560-5. PubMed ID: 19595366
    [TBL] [Abstract][Full Text] [Related]  

  • 40. The Philadelphia story: the 22q11.2 deletion: report on 250 patients.
    McDonald-McGinn DM; Kirschner R; Goldmuntz E; Sullivan K; Eicher P; Gerdes M; Moss E; Solot C; Wang P; Jacobs I; Handler S; Knightly C; Heher K; Wilson M; Ming JE; Grace K; Driscoll D; Pasquariello P; Randall P; Larossa D; Emanuel BS; Zackai EH
    Genet Couns; 1999; 10(1):11-24. PubMed ID: 10191425
    [TBL] [Abstract][Full Text] [Related]  

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