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Journal Abstract Search

116 related items for PubMed ID: 8730297

  • 21. Monozygotic twins with 22q11 deletion and discordant phenotypes.
    Fryer A.
    J Med Genet; 1996 Feb; 33(2):173. PubMed ID: 8929959
    [No Abstract] [Full Text] [Related]

  • 22. Increased incidence of renal anomalies in patients with chromosome 22q11 microdeletion.
    Stewart TL, Irons MB, Cowan JM, Bianchi DW.
    Teratology; 1999 Jan; 59(1):20-2. PubMed ID: 9988879
    [Abstract] [Full Text] [Related]

  • 23. [Hereditary kidney diseases in children (a review of the literature)].
    Degtiareva EM.
    Vopr Okhr Materin Det; 1973 Mar; 18(3):36-40. PubMed ID: 4585577
    [No Abstract] [Full Text] [Related]

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  • 27. Prenatal diagnosis of urinary tract abnormalities--ultrasound and laboratory assessment to predict fetal outcome.
    Antsaklis AJ, Papantoniou NE, Varvarigos JE, Rodolakis AJ, Mesogitis SJ, Aravantinos ID.
    Prog Clin Biol Res; 1989 Mar; 305():19-23. PubMed ID: 2668972
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  • 28. [Chromosome 22q11 deletion syndrome and its relevance for child and adolescent psychiatry. An overview of etiology, physical symptoms, aspects of child development and psychiatric disorders].
    Briegel W, Cohen M.
    Z Kinder Jugendpsychiatr Psychother; 2004 May; 32(2):107-15. PubMed ID: 15181786
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  • 30. Frontonasal malformation and deletion of 22q11.
    Kirkpatrick SJ, Pauli RM.
    Am J Med Genet; 1998 Feb 03; 75(4):443-4. PubMed ID: 9482658
    [No Abstract] [Full Text] [Related]

  • 31. A case of 22q11.2 deletion syndrome with right microphthalmia and left corneal staphyloma.
    Tarlan B, Kiratli H, Kılıç E, Utine E, Boduroğlu K.
    Ophthalmic Genet; 2014 Dec 03; 35(4):248-51. PubMed ID: 23834556
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  • 36. DiGeorge syndrome and related syndromes associated with 22q11.2 deletions. A review.
    Demczuk S, Aurias A.
    Ann Genet; 1995 Dec 03; 38(2):59-76. PubMed ID: 7486827
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  • 38. [Congenital malformations of the kidneys and the deferrent urinary tract].
    Brandis M.
    Kinderkrankenschwester; 1994 Mar 03; 13(3):74-5. PubMed ID: 8193029
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  • 40. Renal function studies in an infant with 4p (-) syndrome.
    Schoeneman M, Nitowsky MM.
    J Med Genet; 1976 Dec 03; 13(6):522-5. PubMed ID: 1018312
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