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	41.	Branchio-oculo-facial syndrome associated with a white forelock. [electronic resource] by Mégarbané, A Hawat, N Chedid, P Bleik, J Délézoïde, A L Producer: 19981015 In: Clinical dysmorphology vol. 7 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	42.	Short stature, abnormal face, joint laxity, dislocation, hernias, delayed bone age, and severe psychomotor retardation in two brothers: previously undescribed MCA/MR syndrome. [electronic resource] by Mégarbané, A Ruchoux, M M Loeys, B Ayoub, N Nuytinck, L Producer: 20020115 In: American journal of medical genetics vol. 104 Availability: No items available. Save to lists Add to cart (remove)
	43.	Primary hypergonadotropic hypogonadism, partial alopecia, and Müllerian hypoplasia: report of a second family with additional findings. [electronic resource] by Mégarbané, A Gannagé-Yared, M H Khalifé, A A Fabre, M Producer: 20040130 In: American journal of medical genetics. Part A vol. 119A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	44.	Feeding problems and gastrointestinal diseases in Down syndrome. [electronic resource] by Ravel, A Mircher, C Rebillat, A-S Cieuta-Walti, C Megarbane, A Producer: 20201109 In: Archives de pediatrie : organe officiel de la Societe francaise de pediatrie vol. 27 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	45.	Two sibs with myoclonic epilepsy, congenital deafness, macular dystrophy, and psychiatric disorders. [electronic resource] by Mégarbané, A Khalil, G Waked, N Rötig, A Caillaud, C Loiselet, J Producer: 19991222 In: American journal of medical genetics vol. 87 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	46.	Exclusion of chromosome 15q21.1 in autosomal-recessive Weill-Marchesani syndrome in an inbred Lebanese family. [electronic resource] by Mégarbané, A Mustapha, M Bleik, J Waked, N Delague, V Loiselet, J Producer: 20010222 In: Clinical genetics vol. 58 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	47.	Trisomy for the distal segment of the short arm of chromosome 17 in a boy with mild mental retardation and some dysmorphic features. [electronic resource] by Mégarbané, A Souraty, N Theophile, D Vekemans, M Samaras, L Ghorayeb, Z Producer: 19970610 In: Annales de genetique vol. 40 Availability: No items available. Save to lists Add to cart (remove)
	48.	Differences in purine metabolism in patients with Down's syndrome. [electronic resource] by Peeters, M A Megarbane, A Cattaneo, F Rethore, M O Lejeune, J Producer: 19940414 In: Journal of intellectual disability research : JIDR vol. 37 ( Pt 6) Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	49.	Linear and whorled nevoid hypermelanosis with bilateral giant cerebral aneurysms. [electronic resource] by Mégarbané, A Vabres, P Slaba, S Smahi, A Loeys, B Okais, N Producer: 20030304 In: American journal of medical genetics vol. 112 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	50.	HLA-C molecular characterization of a Lebanese population and genetic structure of 39 populations from Europe to India-Pakistan. [electronic resource] by Buhler, S Megarbane, A Lefranc, G Tiercy, J-M Sanchez-Mazas, A Producer: 20060825 In: Tissue antigens vol. 68 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	51.	[Announcement of diagnosis of 21-trisomy and abandonment]. [electronic resource] by Mégarbane, A Jobert, A S Rethore, M O Lejeune, J Peeters, M Producer: 19950309 In: Archives de pediatrie : organe officiel de la Societe francaise de pediatrie vol. 1 Availability: No items available. Save to lists Add to cart (remove)
	52.	Microcephaly, colobomatous microphthalmia, short stature, and severe psychomotor retardation in two male cousins: a new MCA/MR syndrome? [electronic resource] by Mégarbané, A Haddad-Zebouni, S Nabbout, R Khoury, A H Traboulsi, E I Producer: 19990730 In: American journal of medical genetics vol. 83 Availability: No items available. Save to lists Add to cart (remove)
	53.	[Mirror hand deformity: a new phenotype with literature review]. [electronic resource] by El Hage, S Ghanem, I Megarbané, A Razzouk, C Dagher, F Kharrat, K Producer: 20080627 In: Revue de chirurgie orthopedique et reparatrice de l'appareil moteur vol. 94 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	54.	Mild Campomelic Dysplasia: Report on a Case and Review. [electronic resource] by Corbani, S Chouery, E Eid, B Jalkh, N Ghoch, J Abou Mégarbané, A Publication details: Molecular syndromology Jan 2011 In: Molecular syndromology vol. 1 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	55.	Cystic fibrosis in Lebanon: distribution of CFTR mutations among Arab communities. [electronic resource] by Desgeorges, M Mégarbané, A Guittard, C Carles, S Loiselet, J Demaille, J Claustres, M Producer: 19970908 In: Human genetics vol. 100 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	56.	Metabolic anomalies in cri du chat syndrome (5p-) lymphocytes and de novo purine synthesis. [electronic resource] by Peeters, M A Rethoré, M O Aris, L Megarbane, A Cattaneo, F Lejeune, J Producer: 19920521 In: Annales de genetique vol. 34 Availability: No items available. Save to lists Add to cart (remove)
	57.	Autosomal dominant secundum atrial septal defect with various cardiac and noncardiac defects: a new midline disorder. [electronic resource] by Mégarbané, A Stephan, E Kassab, R Ashoush, R Salem, N Bouvagnet, P Loiselet, J Producer: 19990506 In: American journal of medical genetics vol. 83 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	58.	Rapid fluorescence in situ hybridization on interphasic nuclei to discriminate between homozygous and heterozygous transgenic mice. [electronic resource] by Paris, D Toyama, K Mégarbané, A Casanova, P M Sinet, P M London, J Producer: 19961210 In: Transgenic research vol. 5 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	59.	Brown-Vialetto-Van Laere syndrome in a large inbred Lebanese family: confirmation of autosomal recessive inheritance? [electronic resource] by Mégarbané, A Desguerres, I Rizkallah, E Delague, V Nabbout, R Barois, A Urtizberea, A Producer: 20000524 In: American journal of medical genetics vol. 92 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	60.	[Autosomal dominant Mendelian midline complex. Secundum atrial septal defect associated with cardiac and facial-thoracic defects. A familial case]. [electronic resource] by Stéphan, E Ashoush, R Mégarbané, A Kassab, R Salem, N Loiselet, J Bouvagnet, P Producer: 20000714 In: Archives des maladies du coeur et des vaisseaux vol. 93 Availability: No items available. Save to lists Add to cart (remove)

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Your search returned 111 results.