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	1.	The 18ph+ chromosome heteromorphism. [electronic resource] by Zelante, L Notarangelo, A Dallapiccola, B Producer: 19950406 In: Prenatal diagnosis vol. 14 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Ring chromosome 21 in healthy persons: different consequences in females and in males. [electronic resource] by Dallapiccola, B De Filippis, V Notarangelo, A Perla, G Zelante, L Producer: 19860917 In: Human genetics vol. 73 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Interstitial "de novo" tandem duplication of 7(q31.1-q35): first reported case. [electronic resource] by Zelante, L Croce, A I Grifa, A Notarangelo, A Calvano, S Producer: 20040220 In: Annales de genetique vol. 46 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	On the parental origin of the X's in a prenatally diagnosed 49,XXXXX syndrome. [electronic resource] by Martini, G Carillo, G Catizone, F Notarangelo, A Mingarelli, R Dallapiccola, B Producer: 19940217 In: Prenatal diagnosis vol. 13 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Cytogenetic and molecular analysis of trisomy 9. Case report and review. [electronic resource] by Zelante, L Notarangelo, A Croce, A I Piemontese, M R Gasparini, P Producer: 19940720 In: Annales de genetique vol. 37 Availability: No items available. Save to lists Add to cart (remove)
	6.	A complex mosaicism 45,X/46,X,del(Xq)/46,X,idic(Xq) in a patient with secondary amenorrhea. [electronic resource] by Calvano, S de Cillis, G P Croce, A I Perla, G Notarangelo, A Zelante, L Producer: 20030509 In: Annales de genetique vol. 45 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	Molecular genetics of cystinuria: identification of four new mutations and seven polymorphisms, and evidence for genetic heterogeneity. [electronic resource] by Gasparini, P Calonge, M J Bisceglia, L Purroy, J Dianzani, I Notarangelo, A Rousaud, F Gallucci, M Testar, X Ponzone, A Producer: 19951103 In: American journal of human genetics vol. 57 Availability: No items available. Save to lists Add to cart (remove)
	8.	Fine exon-intron structure of the Fanconi anemia group A (FAA) gene and characterization of two genomic deletions. [electronic resource] by Centra, M Memeo, E d'Apolito, M Savino, M Ianzano, L Notarangelo, A Liu, J Doggett, N A Zelante, L Savoia, A Producer: 19981005 In: Genomics vol. 51 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	The parental origin of hydatidiform moles and blighted ova: molecular probing with hypervariable DNA polymorphisms. [electronic resource] by Trabetti, E Galavotti, R Zanini, L Zardini, E Zatti, N Bernardi, F Notarangelo, A Croce, A I Pignatti, P F Gasparini, P Producer: 19931207 In: Molecular and cellular probes vol. 7 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	10.	MYO6, the human homologue of the gene responsible for deafness in Snell's waltzer mice, is mutated in autosomal dominant nonsyndromic hearing loss. [electronic resource] by Melchionda, S Ahituv, N Bisceglia, L Sobe, T Glaser, F Rabionet, R Arbones, M L Notarangelo, A Di Iorio, E Carella, M Zelante, L Estivill, X Avraham, K B Gasparini, P Producer: 20010906 In: American journal of human genetics vol. 69 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)