Diguanosine 5', 5″'-P¹,P⁴-tetraphosphate causes specific inhibition and desensitization of Artemia trypsin-like proteinase in the hydrolysis of a high-affinity, argine-rich substrateEZQUIETA, B; VALLEJO, C. G.Biochimica et biophysica acta. 1986, Vol 883, Num 2, pp 380-382, issn 0006-3002Article

Neonatal salt-wasting and 11 β-hydroxylase deficiency in a child carrying a homozygous deletion hybrid CYP11B2 (aldosterone synthase)-CYP11B1 (11β-hydroxylase)EZQUIETA, B; LUZURIAAA, Cristina.Clinical genetics. 2004, Vol 66, Num 3, pp 229-235, issn 0009-9163, 7 p.Article

CF2603/4delT, a new frameshift mutation in exon 13 of the cystic fibrosis transmembrane conductance regulator (CFTR) geneEZQUIETA, B; MOLANO, J.Human genetics. 1993, Vol 91, Num 6, pp 614-615, issn 0340-6717Article

The trypsin-like proteinase of Artemia: yolk localization and developmental activationEZQUIETA, B; VALLEJO, C. G.Comparative biochemistry and physiology. B. Comparative biochemistry. 1985, Vol 82, Num 4, pp 731-736, issn 0305-0491Article

Screening for cystic fibrosis mutations in Spanish patientsMOLANO, J; EZQUIETA, B; GRANELL, R et al.Clinica chimica acta. 1994, Vol 226, Num 2, pp 247-253, issn 0009-8981Conference Paper

Analysis of steroid 21-hydroxylase gene mutations in the Spanish populationEZQUIETA, B; OLIVER, A; GRACIA, R et al.Human genetics. 1995, Vol 96, Num 2, pp 198-204, issn 0340-6717Article

Gene duplications in 21-hydroxylase deficiency : the importance of accurate molecular diagnosis in carrier detection and prenatal diagnosisEZQUIETA, B; BENEYTO, M; MUNOZ-PACHECO, R et al.Prenatal diagnosis. 2006, Vol 26, Num 12, pp 1172-1178, issn 0197-3851, 7 p.Article

Microsatellite markers in the indirect analysis of the steroid 21-hydroxylase geneEZQUIETA, B; JARIEGO, C; VARELA, J. M et al.Prenatal diagnosis. 1997, Vol 17, Num 5, pp 429-434, issn 0197-3851Article