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EXPERIENCIA EN LA DETERMINACION DE HEMOGLOBINA A₂ PAR MICROCROMATOGRAFIA EN DEAE CELULOSA = RESULTATS DU DOSAGE DE L'HEMOGLOBINE A₂ PAR MICROCHROMATOGRAPHIE EN DEAE CELLULOSEBAIGET M; GIMFERRER E; RUTLLANT ML et al.1978; SANGRE; ESP; DA. 1978; VOL. 23; NO 6; PP. 864-869; ABS. ENG; BIBL. 4 REF.Article

Aportaciones de la genética molecular al estudio de la patología respiratoriaBAIGET, M; TIZZANO, E.Archivos de bronconeumología. 1991, Vol 27, Num 3, pp 147-152, issn 0300-2896Article

HAEMOGLOBIN LEPORE BOSTON IN A SPANISH FAMILY.GIMFERRER E; BAIGET M; DARBRE PD et al.1976; ACTA HAEMATOL.; SUISSE; DA. 1976; VOL. 56; NO 4; PP. 234-240; BIBL. 1 P. 1/2Article

Carbamazepina como psicoprofiláctico = Carbamazepine as psychoprophylaxisFONSECA FABREGAS, L. E; ARGANY BAIGET, M. A.Psiquis (Madrid). 1995, Vol 16, Num 3, pp 21-28, issn 0210-8348Article

Cell-specific survival motor neuron gene expression during human development of the central nervous system. Implications for the pathogenesis of spinal muscular atrophyTIZZANO, E. F; CABOT, C; BAIGET, M et al.The American journal of pathology. 1998, Vol 153, Num 2, pp 355-361, issn 0002-9440Article

Copy number variations are not modifiers of phenotypic expression in a pair of identical twins carrying a BRCA1 mutationLASA, A; Y CAJAL, T. Ramón; LLORT, G et al.Breast cancer research and treatment. 2010, Vol 123, Num 3, pp 901-905, issn 0167-6806, 5 p.Article

Pharmacogenetic prediction of clinical outcome in advanced colorectal cancer patients receiving oxaliplatin/5-fluorouracil as first-line chemotherapyPARE, L; MARCUELLO, E; ALTES, A et al.British journal of cancer. 2008, Vol 99, Num 7, pp 1050-1055, issn 0007-0920, 6 p.Article

Primary neuroendocrine carcinoma of the skin expresses Tyrosinase mRNA: Detection by a specific nested PCR techniqueALEGRE, M; PUIG, L; CARRENO, R et al.Dermatology (Basel). 1997, Vol 194, Num 4, pp 334-337, issn 1018-8665Conference Paper

Various patterns of chimerism after allogeneic bone marrow transplantation for advanced chronic lymphocytic leukemiaMARTINO, R; BRUNET, S; GARCIA, A et al.Bone marrow transplantation (Basingstoke). 1995, Vol 16, Num 6, pp 783-786, issn 0268-3369Article

Expansion of the myotonic dystrophy gene in italian and Spanish patientsMELCHIONDA, S; COBO, A; DALLAPICCOLA, B et al.Journal of medical genetics. 1992, Vol 29, Num 11, pp 789-790, issn 0022-2593Article

Linkage disequilibrium detected between myotonic dystrophy and the anonymous marker D19S63 in Spanish populationCOBO, A; GRINBERG, D; BALCELLS, S et al.Human genetics. 1992, Vol 89, Num 3, pp 287-291, issn 0340-6717Article

Determination of the spectrum of β-thalassemia genes in Spain by use of dot-blot analysis of amplified β-globin DNAAMSELEM, S; NUNES, V; VIDAUD, M et al.American journal of human genetics. 1988, Vol 43, Num 1, pp 95-100, issn 0002-9297, 6 p.Article

A novel insertional mutation of a single base in exon 12 of the dystrophin geneLASA, A; GALLANO, P; COLOMER, J et al.Clinical genetics. 1995, Vol 48, Num 3, pp 128-130, issn 0009-9163Article

Inversion of intron 22 in isolated cases of severe hemophilia ATIZZANO, E. F; DOMENECH, M; BAIGET, M et al.Thrombosis and haemostasis. 1995, Vol 73, Num 1, pp 6-9, issn 0340-6245Article

Isolated cardiomyopathy caused by a DMD nonsense mutation in somatic mosaicism: genetic normalization in skeletal muscleJUAN-MATEU, J; PARADAS, C; OLIVE, M et al.Clinical genetics. 2012, Vol 82, Num 6, pp 574-578, issn 0009-9163, 5 p.Article

AML-1 mutations outside the RUNT domain: description of two cases in myeloid malignanciesCARNICER, M. J; NOMDEDEU, I. F; LASA, A et al.Leukemia. 2002, Vol 16, Num 11, pp 2329-2332, issn 0887-6924Article

A novel mutation in exon 17 of the β-subunit of rod phosphodiesterase in two RP sisters of a consanguineous familyVALVERDE, D; SOLANS, T; BAIGET, M et al.Human genetics. 1996, Vol 97, Num 1, pp 35-38, issn 0340-6717Article

Homozygous myotonic dystrophy : clinical and molecular studies of three unrelated casesMARTORELL, L; ILLA, I; ROSELL, J et al.Journal of medical genetics. 1996, Vol 33, Num 9, pp 783-785, issn 0022-2593Article

Mutational analysis of RAG-1 in lymphoid malignanciesNOMDEDEU, J; LASA, A; SEMINAGO, R et al.Leukemia. 1996, Vol 10, Num 11, pp 1715-1718, issn 0887-6924Article

Factor VIII gene inversions in severe hemophilia A : results of an international consortium studyANTONARAKIS, S. E; ROSSITER, J. P; GITSCHIER, J et al.Blood. 1995, Vol 86, Num 6, pp 2206-2212, issn 0006-4971Article

Prevalence of myotonic dystrophy in Guipúzcoa (Basque Country, Spain)LOPEZ DE MUNAIN, A; BLANCO, A; EMPARANZA, J. I et al.Neurology. 1993, Vol 43, Num 8, pp 1573-1576, issn 0028-3878Article

Parental origin and germline mosaicism of deletions and duplications of the dystrophin gene : a European studyVAN ESSEN, A. J; ABBS, S; FERRARI, M et al.Human genetics. 1992, Vol 88, Num 3, pp 249-257, issn 0340-6717Article

Hb F-Catalonia or α₂^Gγ₂15(A12)TRP→ARGPLASESKA, D; WILSON, J. B; KUTLAR, F et al.Hemoglobin. 1990, Vol 14, Num 5, pp 511-516, issn 0363-0269, 6 p.Article

Spanish delta-beta-thalassemia: hematological studies and composition of the gamma-chains in ten homozygous patientsBAIGET, M; GIMFERRER, E; FERNANDEZ, I et al.Acta haematologica. 1983, Vol 70, Num 5, pp 341-344, issn 0001-5792Article