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	1.	Frequency of the HFE C282Y and H63D mutations in distinct ethnic groups living in Spain. [electronic resource] by Baiget, M Barceló, M J Gimferrer, E Producer: 19981113 In: Journal of medical genetics vol. 35 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Colorectal cancer and HFE gene mutations. [electronic resource] by Altés, A Gimferrer, E Capella, G Barceló, M J Baiget, M Producer: 19990803 In: Haematologica vol. 84 Availability: No items available. Save to lists Add to cart (remove)
	3.	[Plasma carriers of vitamin B 12 in normal controls and in the initial diagnosis of pernicious anemia]. [electronic resource] by Remacha, A Fornells, J Barceló, M J Ubeda, J Gimferrer, E Producer: 19890622 In: Sangre vol. 33 Availability: No items available. Save to lists Add to cart (remove)
	4.	Prevalence of hemochromatosis related HFE gene mutations in patients with acute myeloid leukemia. [electronic resource] by Gimferrer, E Nomdedeu, J Gich, I Barceló, M J Baiget, M Producer: 19990707 In: Leukemia research vol. 23 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	HFE mutation analysis in patients with hepatitis C virus with positive screening for iron overload. [electronic resource] by Remacha, A F Carrasco, M Sardá, M P Barceló, M J Baiget, M Producer: 19990623 In: Haematologica vol. 84 Availability: No items available. Save to lists Add to cart (remove)
	6.	Prenatal diagnosis for risk of spinal muscular atrophy. [electronic resource] by Cuscó, I Barceló, M J Soler, C Parra, J Baiget, M Tizzano, E Producer: 20021226 In: BJOG : an international journal of obstetrics and gynaecology vol. 109 Availability: No items available. Save to lists Add to cart (remove)
	7.	Genotyping the HFE gene by melting point analysis with the LightCycler system: Pros and cons. [electronic resource] by Bach, V Barceló, M J Altés, A Remacha, A Félez, J Baiget, M Producer: 20070920 In: Blood cells, molecules & diseases vol. 36 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	The deoxyuridine suppression test in peripheral lymphocytes. [electronic resource] by Remacha, A Barceló, M J Pastor, M Ubeda, J Espadaler, M Gimferrer, E Producer: 19900525 In: European journal of haematology vol. 44 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	Serum erythropoietin in the diagnosis of polycythemia vera. A follow-up study. [electronic resource] by Remacha, A F Montserrat, I Santamaria, A Oliver, A Barceló, M J Parellada, M Producer: 19971006 In: Haematologica vol. 82 Availability: No items available. Save to lists Add to cart (remove)
	10.	Autosomal dominant hereditary hemochromatosis associated with two novel Ferroportin 1 mutations in Spain. [electronic resource] by Bach, V Remacha, A Altés, A Barceló, M J Molina, M A Baiget, M Producer: 20060504 In: Blood cells, molecules & diseases vol. 36 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	11.	The S65C mutation in Spain. Implications for iron overload screening. [electronic resource] by Remacha, A F Barceló, M J Sardà, M P Blesa, I Altés, A Baiget, M Producer: 20010510 In: Haematologica vol. 85 Availability: No items available. Save to lists Add to cart (remove)
	12.	The deoxyuridine suppression test in HIV-1 positive patients: the role of azydothymidine (AZT). [electronic resource] by García-Die, F Remacha, A Cadafalch, J Barceló, M J Parellada, M M Arza, B Producer: 19960718 In: European journal of haematology vol. 56 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	13.	Evaluation of erythropoietin in endurance runners. [electronic resource] by Remacha, A F Ordoñez, J Barcelo, M J Garcia-Die, F Arza, B Estruch, A Producer: 19950130 In: Haematologica vol. 79 Availability: No items available. Save to lists Add to cart (remove)
	14.	Screening for iron overload and HFE mutations in a university hospital. [electronic resource] by Remacha, A F Carrasco, M Sardà, M P Barceló, M J Blesa, I Baiget, M Producer: 20001205 In: Haematologica vol. 85 Availability: No items available. Save to lists Add to cart (remove)
	15.	Congenital intrinsic factor deficiency in a Spanish patient. [electronic resource] by Remacha, A F Sambeat, M A Barceló, M J Mones, J García-Die, J Gimferrer, E Producer: 19920618 In: Annals of hematology vol. 64 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	16.	[Interest in the study of genetic variants of the promoter region of the UGT1A1 gene in neonatal jaundice]. [electronic resource] by Seco, M L del Río, E Barceló, M J Remacha, A Ginovart, G Moliner, E Baiget, M Producer: 20020611 In: Anales espanoles de pediatria vol. 56 Availability: No items available. Save to lists Add to cart (remove)
	17.	Survival and respiratory decline are not related to homozygous SMN2 deletions in ALS patients. [electronic resource] by Gamez, J Barceló, M J Muñoz, X Carmona, F Cuscó, I Baiget, M Cervera, C Tizzano, E F Producer: 20021209 In: Neurology vol. 59 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	18.	[Influence of chronic renal failure and of its treatment on serum erythropoietin]. [electronic resource] by Remacha, A F Oliver, A Calero, F Barceló, M J Doñate, T Ballarín, J A García-Die, F Producer: 19920827 In: Medicina clinica vol. 99 Availability: No items available. Save to lists Add to cart (remove)
	19.	Characterisation of SMN hybrid genes in Spanish SMA patients: de novo, homozygous and compound heterozygous cases. [electronic resource] by Cuscó, I Barceló, M J del Rio, E Martín, Y Hernández-Chico, C Bussaglia, E Baiget, M Tizzano, E F Producer: 20010531 In: Human genetics vol. 108 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	20.	SMN2 copy number predicts acute or chronic spinal muscular atrophy but does not account for intrafamilial variability in siblings. [electronic resource] by Cuscó, I Barceló, M J Rojas-García, R Illa, I Gámez, J Cervera, C Pou, A Izquierdo, G Baiget, M Tizzano, E F Producer: 20060929 In: Journal of neurology vol. 253 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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Your search returned 23 results.