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	1.	Identification of trophoblast in chorionic villi biopsy samples. [electronic resource] by Covone, A E Johnson, P M Producer: 19860326 In: Human genetics vol. 72 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Screening Duchenne and Becker muscular dystrophy patients for deletions in 30 exons of the dystrophin gene by three-multiplex PCR. [electronic resource] by Covone, A E Caroli, F Romeo, G Producer: 19920910 In: American journal of human genetics vol. 51 Availability: No items available. Save to lists Add to cart (remove)
	3.	Genotype-phenotype correlation and germline mosaicism in DMD/BMD patients with deletions of the dystrophin gene. [electronic resource] by Covone, A E Lerone, M Romeo, G Producer: 19910912 In: Human genetics vol. 87 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Trophoblast cells in peripheral blood from pregnant women. [electronic resource] by Covone, A E Mutton, D Johnson, P M Adinolfi, M Producer: 19841119 In: Lancet (London, England) vol. 2 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	[Identification of the dystrophin gene deletions in DMD/BMD patients. Analysis of the reading frame shift and germinal mosaicism]. [electronic resource] by Covone, A E Caroli, F Cereseto, A Lerone, M Romeo, G Producer: 19910916 In: Minerva pediatrica vol. 43 Availability: No items available. Save to lists Add to cart (remove)
	6.	Analysis of peripheral maternal blood samples for the presence of placenta-derived cells using Y-specific probes and McAb H315. [electronic resource] by Covone, A E Kozma, R Johnson, P M Latt, S A Adinolfi, M Producer: 19890203 In: Prenatal diagnosis vol. 8 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	WES in a family trio suggests involvement of TECPR2 in a complex form of progressive motor neuron disease. [electronic resource] by Covone, A E Fiorillo, C Acquaviva, M Trucco, F Morana, G Ravazzolo, R Minetti, C Producer: 20170522 In: Clinical genetics vol. 90 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	Deleted and normal chromosome 10 homologs from a patient with Hirschsprung disease isolated in two cell hybrids through enrichment by immunomagnetic selection. [electronic resource] by Puliti, A Covone, A E Bicocchi, M P Bolino, A Lerone, M Martucciello, G Jasonni, V Romeo, G Producer: 19930513 In: Cytogenetics and cell genetics vol. 63 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	DNA technology for prenatal diagnosis of cystic fibrosis in Italy. [electronic resource] by Seia, M Cozzi, G Sereni, L Ferrari, M Cremonesi, L Covone, A E Fenu, L Ronchetto, P Devoto, M Romeo, G Producer: 19911209 In: Advances in experimental medicine and biology vol. 290 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	10.	SSCP detection of novel mutations in patients with Emery-Dreifuss muscular dystrophy: definition of a small C-terminal region required for emerin function. [electronic resource] by Nigro, V Bruni, P Ciccodicola, A Politano, L Nigro, G Piluso, G Cappa, V Covone, A E Romeo, G D'Urso, M Producer: 19960418 In: Human molecular genetics vol. 4 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	11.	Parental origin and germline mosaicism of deletions and duplications of the dystrophin gene: a European study. [electronic resource] by van Essen, A J Abbs, S Baiget, M Bakker, E Boileau, C van Broeckhoven, C Bushby, K Clarke, A Claustres, M Covone, A E Producer: 19920304 In: Human genetics vol. 88 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	12.	A report on 528 intragenic deletions detected in DMD and BMD patients by an Italian collaborative study. [electronic resource] by Mioni, F Danieli, G A Cao, A Cau, M Colonna-Romano, S Covone, A E De Leonardis, P De Leo, R Esposito, M G Felicetti, L Producer: 19950829 In: Gene geography : a computerized bulletin on human gene frequencies vol. 8 Availability: No items available. Save to lists Add to cart (remove)
	13.	Diagnosis of Duchenne and Becker muscular dystrophies by polymerase chain reaction. A multicenter study. [electronic resource] by Chamberlain, J S Chamberlain, J R Fenwick, R G Ward, P A Caskey, C T Dimnik, L S Bech-Hansen, N T Hoar, D I Richards, S Covone, A E Govanni, R Abbs, S Bentley, D R Bobrow, M Rysiecki, G Ray, P N Boileau, C Junien, C Boehm, C Venne, V L Fujmura, F K Spiga, I Ferrari, M Tedeschi, S Bakker, E Kneppers, A L van Ommen, G J Jain, K Spector, E Crandall, B Kiuru, A Savontaus, M L Caskey, C T Chamberlain, J S Chamberlain, J R Rysiecki, G Producer: 19920602 In: JAMA vol. 267 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	14.	The molecular basis for Duchenne versus Becker muscular dystrophy: correlation of severity with type of deletion. [electronic resource] by Koenig, M Beggs, A H Moyer, M Scherpf, S Heindrich, K Bettecken, T Meng, G Müller, C R Lindlöf, M Kaariainen, H de la Chapellet, A Kiuru, A Savontaus, M L Gilgenkrantz, H Récan, D Chelly, J Kaplan, J C Covone, A E Archidiacono, N Romeo, G Liechti-Gailati, S Schneider, V Braga, S Moser, H Darras, B T Murphy, P Francke, U Chen, J D Morgan, G Denton, M Greenberg, C R Wrogemann, K Blonden, L A van Paassen, M B van Ommen, G J Kunkel, L M Producer: 19910918 In: American journal of human genetics vol. 45 Availability: No items available. Save to lists Add to cart (remove)