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Results: 1-25 | 26-29 |
Results: 26-29/29
Autosomal dominant secundum atrial septal defect with various cardiac and noncardiac defects: A new midline disorder
Authors: Megarbane, A Stephan, E Kassab, R Ashoush, R Salem, N Bouvagnet, P Loiselet, J
Citation: A. Megarbane et al., Autosomal dominant secundum atrial septal defect with various cardiac and noncardiac defects: A new midline disorder, AM J MED G, 83(3), 1999, pp. 193-200
Microcephaly, colobomatous microphthalmia, short stature, and severe psychomotor retardation in two male cousins: A new MCA/MR syndrome?
Authors: Megarbane, A Haddad-Zebouni, S Nabbout, R Khoury, AH Traboulsi, EI
Citation: A. Megarbane et al., Microcephaly, colobomatous microphthalmia, short stature, and severe psychomotor retardation in two male cousins: A new MCA/MR syndrome?, AM J MED G, 83(2), 1999, pp. 82-87
Microcephaly, microphthalmia, congenital cataract, optic atrophy, short stature, hypotonia, severe psychomotor retardation, and cerebral malformations: a second family with micro syndrome or a new syndrome?
Authors: Megarbane, A Choueiri, R Bleik, J Mezzina, M Caillaud, C
Citation: A. Megarbane et al., Microcephaly, microphthalmia, congenital cataract, optic atrophy, short stature, hypotonia, severe psychomotor retardation, and cerebral malformations: a second family with micro syndrome or a new syndrome?, J MED GENET, 36(8), 1999, pp. 637-640
Homozygosity for a novel DTDST mutation in a child with a 'broad bone-platyspondylic' variant of diastrophic dysplasia
Authors: Megarbane, A Haddad, FA Haddad-Zebouni, S Achram, M Eich, G Le Merrer, M Superti-Furga, A
Citation: A. Megarbane et al., Homozygosity for a novel DTDST mutation in a child with a 'broad bone-platyspondylic' variant of diastrophic dysplasia, CLIN GENET, 56(1), 1999, pp. 71-76
Risultati: 1-25 | 26-29 |