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Results:
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Results: 2
Chromosome 22-specific low copy repeats and the 22q11.2 deletion syndrome:genomic organization and deletion endpoint analysis
Authors:
Shaikh, TH Kurahashi, H Saitta, SC O'Hare, AM Hu, P Roe, BA Driscoll, DA McDonald-McGinn, DM Zackai, EH Budarf, ML Emanuel, BS
Citation:
Th. Shaikh et al., Chromosome 22-specific low copy repeats and the 22q11.2 deletion syndrome:genomic organization and deletion endpoint analysis, HUM MOL GEN, 9(4), 2000, pp. 489-501
A 22q11.2 deletion that excludes UFD1L and CDC45L in a patient with conotruncal and craniofacial defects
Authors:
Saitta, SC McGrath, JM Mensch, H Shaikh, TH Zackai, EH Emanuel, BS
Citation:
Sc. Saitta et al., A 22q11.2 deletion that excludes UFD1L and CDC45L in a patient with conotruncal and craniofacial defects, AM J HU GEN, 65(2), 1999, pp. 562-566
Risultati:
1-2
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