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Journal Abstract Search

260 related items for PubMed ID: 10631928

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  • 2. [Neonatal hypocalcaemic dilated myocardiopathy due to a 22q11 microdeletion].
    Goulet M, Rio M, Jacquette A, Ladouceur M, Bonnet D.
    Arch Mal Coeur Vaiss; 2006 May; 99(5):520-2. PubMed ID: 16802747
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  • 7. Hypoparathyroidism as the major manifestation in two patients with 22q11 deletions.
    Scirè G, Dallapiccola B, Iannetti P, Bonaiuto F, Galasso C, Mingarelli R, Boscherini B.
    Am J Med Genet; 1994 Oct 01; 52(4):478-82. PubMed ID: 7747762
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  • 8. 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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  • 9. Endocrine manifestations of chromosome 22q11.2 microdeletion syndrome.
    Choi JH, Shin YL, Kim GH, Seo EJ, Kim Y, Park IS, Yoo HW.
    Horm Res; 2005 Oct 03; 63(6):294-9. PubMed ID: 15995343
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  • 15. Fragile X syndrome and 22q11.2 microdeletion in the same sibship.
    Missirian C, Moncla A, Voelckel MA, Ravix V, Philip N.
    Am J Med Genet; 2000 Dec 11; 95(4):358-60. PubMed ID: 11186890
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  • 16. 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 11; 16(3):226-30. PubMed ID: 15853951
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  • 18. [Cerebral polymicrogyria and 22q11 deletion syndrome].
    Arriola-Pereda G, Verdú-Pérez A, de Castro-De Castro P.
    Rev Neurol; 2005 May 11; 48(4):188-90. PubMed ID: 19226486
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  • 19. [Phenotypic variability of deletion 22q11.2. An analysis of 16 observations with special emphasis on the neurological manifestations].
    Eirís-Puñal J, Iglesias-Meleiro JM, Blanco-Barca MO, Fuster-Siebert M, Barros-Angueira F, Ansede A, Castro-Gago M.
    Rev Neurol; 2005 May 11; 37(7):601-7. PubMed ID: 14582013
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