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Results: 1-9 |
Results: 9
Association of chromosome 22q11 deletion with isolated anomalies of aorticarch laterality and branching
Authors: McElhinney, DB Clark, BJ Weinberg, PM Kenton, ML McDonald-McGinn, D Driscoll, DA Zackai, EH Goldmuntz, E
Citation: Db. Mcelhinney et al., Association of chromosome 22q11 deletion with isolated anomalies of aorticarch laterality and branching, J AM COL C, 37(8), 2001, pp. 2114-2119
Patterns of right aortic arch and mirror-image branching of the brachiocephalic vessels without associated anomalies
Authors: McElhinney, DB Hoydu, AK Gaynor, JW Spray, TL Goldmuntz, E Weinberg, PM
Citation: Db. Mcelhinney et al., Patterns of right aortic arch and mirror-image branching of the brachiocephalic vessels without associated anomalies, PEDIAT CARD, 22(4), 2001, pp. 285-291
The epidemiology and genetics of congenital heart disease
Authors: Goldmuntz, E
Citation: E. Goldmuntz, The epidemiology and genetics of congenital heart disease, CLIN PERIN, 28(1), 2001, pp. 1
Cardiovascular anomalies in patients diagnosed with a chromosome 22q11 deletion beyond 6 months of age
Authors: McElhinney, DB Mcdonald-McGinn, D Zackai, EH Goldmuntz, E
Citation: Db. Mcelhinney et al., Cardiovascular anomalies in patients diagnosed with a chromosome 22q11 deletion beyond 6 months of age, PEDIATRICS, 108(6), 2001, pp. NIL_47-NIL_50
NKX2.5 mutations in patients with tetralogy of Fallot
Authors: Goldmuntz, E Geiger, E Benson, DW
Citation: E. Goldmuntz et al., NKX2.5 mutations in patients with tetralogy of Fallot, CIRCULATION, 104(21), 2001, pp. 2565-2568
Guidelines for 22q11 deletion screening of patients with conotruncal defects - Reply
Authors: Goldmuntz, E Clark, BJ Mitchell, LE Cuneo, BF McDonald-McGinn, D Zackair, EH Emanuel, BS Driscoll, DA
Citation: E. Goldmuntz et al., Guidelines for 22q11 deletion screening of patients with conotruncal defects - Reply, J AM COL C, 33(6), 1999, pp. 1747-1748
Features of Alagille syndrome in 92 patients: Frequency and relation to prognosis
Authors: Emerick, KM Rand, EB Goldmuntz, E Krantz, ID Spinner, NB Piccoli, DA
Citation: Km. Emerick et al., Features of Alagille syndrome in 92 patients: Frequency and relation to prognosis, HEPATOLOGY, 29(3), 1999, pp. 822-829
Cognitive and behavior profile of preschool children with chromosome 22q11.2 deletion
Authors: Gerdes, M Solot, C Wang, PP Moss, E LaRossa, D Randall, P Goldmuntz, E Clark, BJ Driscoll, DA Jawad, A Emanuel, BS McDonald-McGinn, DM Batshaw, ML Zackai, EH
Citation: M. Gerdes et al., Cognitive and behavior profile of preschool children with chromosome 22q11.2 deletion, AM J MED G, 85(2), 1999, pp. 127-133
Jagged1 mutations in patients ascertained with isolated congenital heart defects
Authors: Krantz, ID Smith, R Colliton, RP Tinkel, H Zackai, EH Piccoli, DA Goldmuntz, E Spinner, NB
Citation: Id. Krantz et al., Jagged1 mutations in patients ascertained with isolated congenital heart defects, AM J MED G, 84(1), 1999, pp. 56-60
Risultati: 1-9 |