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92 results

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Page 1
Communication issues in 22q11.2 deletion syndrome: children at risk.
Solot CB, Gerdes M, Kirschner RE, McDonald-McGinn DM, Moss E, Woodin M, Aleman D, Zackai EH, Wang PP. Solot CB, et al. Among authors: kirschner re. Genet Med. 2001 Jan-Feb;3(1):67-71. doi: 10.1097/00125817-200101000-00015. Genet Med. 2001. PMID: 11339383 Free article.
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. McDonald-McGinn DM, et al. Genet Couns. 1999;10(1):11-24. Genet Couns. 1999. PMID: 10191425
Cleft palate repair at 3 to 7 months of age.
Kirschner RE, Randall P, Wang P, Jawad AF, Duran M, Huang K, Solot C, Cohen M, LaRossa D. Kirschner RE, et al. Plast Reconstr Surg. 2000 May;105(6):2127-32. doi: 10.1097/00006534-200005000-00032. Plast Reconstr Surg. 2000. PMID: 10839414
Otolaryngologic manifestations of the 22q11.2 deletion syndrome.
Dyce O, McDonald-McGinn D, Kirschner RE, Zackai E, Young K, Jacobs IN. Dyce O, et al. Among authors: kirschner re. Arch Otolaryngol Head Neck Surg. 2002 Dec;128(12):1408-12. doi: 10.1001/archotol.128.12.1408. Arch Otolaryngol Head Neck Surg. 2002. PMID: 12479730
The 22q11.2 deletion in African-American patients: an underdiagnosed population?
McDonald-McGinn DM, Minugh-Purvis N, Kirschner RE, Jawad A, Tonnesen MK, Catanzaro JR, Goldmuntz E, Driscoll D, Larossa D, Emanuel BS, Zackai EH. McDonald-McGinn DM, et al. Among authors: kirschner re. Am J Med Genet A. 2005 Apr 30;134(3):242-6. doi: 10.1002/ajmg.a.30069. Am J Med Genet A. 2005. PMID: 15754359 Free PMC article.
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 Jr, LaRossa D, Bartlett SP, Whitaker LA, Zackai EH. McDonald-McGinn DM, et al. Among authors: kirschner re. Am J Med Genet A. 2005 Aug 1;136A(4):358-62. doi: 10.1002/ajmg.a.30746. Am J Med Genet A. 2005. PMID: 16001439
92 results