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	1.	[Nifedipine-captopril combination in the treatment of refractory arterial hypertension]. [electronic resource] by Cosenzi, A Franca, G Piemontesi, A M Sancandi, M Bellini, G Producer: 19870924 In: Giornale di clinica medica vol. 67 Availability: No items available. Save to lists Add to cart (remove)
	2.	Assignment of the HOX11L2 gene to human chromosome band 5q35.1 and of its murine homolog to mouse chromosome bands 11A4-A5 by in situ hybridization. [electronic resource] by Cinti, R Fava, M Sancandi, M Matera, I Ravazzolo, R Ceccherini, I Producer: 20010802 In: Cytogenetics and cell genetics vol. 92 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	A single-nucleotide polymorphic variant of the RET proto-oncogene is underrepresented in sporadic Hirschsprung disease. [electronic resource] by Griseri, P Sancandi, M Patrone, G Bocciardi, R Hofstra, R Ravazzolo, R Devoto, M Romeo, G Ceccherini, I Producer: 20001012 In: European journal of human genetics : EJHG vol. 8 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	A heterozygous endothelin 3 mutation in Waardenburg-Hirschsprung disease: is there a dosage effect of EDN3/EDNRB gene mutations on neurocristopathy phenotypes? [electronic resource] by Pingault, V Bondurand, N Lemort, N Sancandi, M Ceccherini, I Hugot, J P Jouk, P S Goossens, M Producer: 20010614 In: Journal of medical genetics vol. 38 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Evaluation of the HOX11L1 gene as a candidate for congenital disorders of intestinal innervation. [electronic resource] by Costa, M Fava, M Seri, M Cusano, R Sancandi, M Forabosco, P Lerone, M Martucciello, G Romeo, G Ceccherini, I Producer: 20000822 In: Journal of medical genetics vol. 37 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Single nucleotide polymorphic alleles in the 5' region of the RET proto-oncogene define a risk haplotype in Hirschsprung's disease. [electronic resource] by Sancandi, M Griseri, P Pesce, B Patrone, G Puppo, F Lerone, M Martucciello, G Romeo, G Ravazzolo, R Devoto, M Ceccherini, I Producer: 20030930 In: Journal of medical genetics vol. 40 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	Incidence of RET mutations in patients with Hirschsprung's disease. [electronic resource] by Sancandi, M Ceccherini, I Costa, M Fava, M Chen, B Wu, Y Hofstra, R Laurie, T Griffths, M Burge, D Tam, P K Producer: 20000203 In: Journal of pediatric surgery vol. 35 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)