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Journal Abstract Search

132 related items for PubMed ID: 12465167

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  • 3. The 22q11.2 deletion syndrome: more answers but more questions.
    Fernhoff PM.
    J Pediatr; 2000 Aug; 137(2):145-7. PubMed ID: 10931401
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  • 4. Allergies in patients with chromosome 22q11.2 deletion syndrome (DiGeorge syndrome/velocardiofacial syndrome) and patients with chronic granulomatous disease.
    Staple L, Andrews T, McDonald-McGinn D, Zackai E, Sullivan KE.
    Pediatr Allergy Immunol; 2005 May; 16(3):226-30. PubMed ID: 15853951
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  • 5. The phenotypic spectrum of the 10p deletion syndrome versus the classical DiGeorge syndrome.
    Van Esch H, Groenen P, Fryns JP, Van de Ven W, Devriendt K.
    Genet Couns; 1999 May; 10(1):59-65. PubMed ID: 10191430
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  • 6. [Study on clinical features and fluorescence in situ hybridization detections of 22q11 microdeletion syndrome].
    Qin YF, Yang JB, Xie CH, Shao J, Zhao ZY.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2007 Jun; 24(3):284-7. PubMed ID: 17557238
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  • 7. Deletion of chromosome 22q11 and pseudohypoparathyroidism.
    Craigen WJ, Lindsay EA, Bricker JT, Hawkins EP, Baldini A.
    Am J Med Genet; 1997 Oct 03; 72(1):63-5. PubMed ID: 9295077
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  • 16. Hypocalcemia and chromosome 22q11 microdeletion.
    Garabédian M.
    Genet Couns; 1999 Oct 03; 10(4):389-94. PubMed ID: 10631928
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  • 17. The human genome: chromosome 22q11 deletion syndrome.
    Morris-Rosendahl DJ, Back E.
    Am J Psychiatry; 2002 Apr 03; 159(4):527. PubMed ID: 11925287
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  • 18. [Monosomy 22pter-22q11.2 with monosomy 10q26.2-10qter without Di George syndrome].
    Arslanian A, Veneziano G, Grasso M, Brugo A, Bertamino F.
    Pathologica; 1985 Apr 03; 77(1052):767-70. PubMed ID: 3842998
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  • 19. Atypical deletion of 22q11.2: detection using the FISH TBX1 probe and molecular characterization with high-density SNP arrays.
    Beaujard MP, Chantot S, Dubois M, Keren B, Carpentier W, Mabboux P, Whalen S, Vodovar M, Siffroi JP, Portnoï MF.
    Eur J Med Genet; 2009 Apr 03; 52(5):321-7. PubMed ID: 19467348
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