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Journal Abstract Search

135 related items for PubMed ID: 16001439

  • 1. Craniosynostosis: another feature of the 22q11.2 deletion syndrome.
    McDonald-McGinn DM, Gripp KW, Kirschner RE, Maisenbacher MK, Hustead V, Schauer GM, Keppler-Noreuil KM, Ciprero KL, Pasquariello P, LaRossa D, Bartlett SP, Whitaker LA, Zackai EH.
    Am J Med Genet A; 2005 Aug 01; 136A(4):358-62. PubMed ID: 16001439
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  • 3. Partial craniosynostosis in a patient with deletion 22q11.
    Karteszi J, Kress W, Szasz M, Czako M, Melegh B, Kosztolanyi GY, Morava E.
    Genet Couns; 2004 Aug 01; 15(4):481-3. PubMed ID: 15658627
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  • 4. Severe craniosynostosis in an infant with deletion 22q11.2 syndrome.
    Al-Hertani W, Hastings VA, McGowan-Jordan J, Hurteau J, Graham GE.
    Am J Med Genet A; 2013 Jan 01; 161A(1):153-7. PubMed ID: 23239640
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  • 5. Pathogenic variants in CDC45 on the remaining allele in patients with a chromosome 22q11.2 deletion result in a novel autosomal recessive condition.
    Unolt M, Kammoun M, Nowakowska B, Graham GE, Crowley TB, Hestand MS, Demaerel W, Geremek M, Emanuel BS, Zackai EH, Vermeesch JR, McDonald-McGinn D.
    Genet Med; 2020 Feb 01; 22(2):326-335. PubMed ID: 31474763
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  • 9. Craniosynostosis in an infant with an interstitial deletion of 15q [46,XY,del(15)(q15q22.1)].
    Fukushima Y, Wakui K, Nishida T, Nishimoto H.
    Am J Med Genet; 1990 Jun 01; 36(2):209-13. PubMed ID: 2368808
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  • 16. Chromosome 7 short arm deletion and craniosynostosis. A 7p-syndrome.
    Gong BT, Norwood TH, Hoehn H, McPherson E, Hall JG, Hickman R.
    Hum Genet; 1976 Dec 29; 35(1):117-23. PubMed ID: 1002161
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  • 20. Pre- and Postnatal Diagnosis of 10p14 Deletion and 22q11.2 Deletion Syndrome and Significance of Non-Cardiac Markers.
    Shetty M, Srikanth A, Kadandale J, Hegde S.
    Cytogenet Genome Res; 2016 Dec 29; 148(4):249-55. PubMed ID: 27300488
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