EFECTOS DE LA PRESION DE SOBRECARGA SOBRE LA PERMEABILIDAD ABSOLUTA EN ALGUNAS MUESTRAS DE LA FORMACION SAN ANDRES (MEXICO).LLOVERA MA; VILLAMAR M.1969; REV. INST. MEX. PETROLEO; MEX; 1969(10), VOL. 1, NUM. 0004, P. 53 A 58Miscellaneous

Crossover in a Spanish cystic fibrosis familyFERNANDEZ, E; VILLAMAR, M; BENITEZ, J et al.Human genetics. 1990, Vol 86, Num 1, issn 0340-6717, p. 102Article

Linkage disequilibrium between cystic fibrosis locus and three DNA markers, XV-2c, KM19 and MP6d-9, in 43 spannish familiesFERNANDEZ, E; BENITEZ, J; VILLAMAR, M et al.Human genetics. 1990, Vol 84, Num 4, pp 379-380, issn 0340-6717Article

Study of the parental origin of sexual aneuploidy in ten families using RFLPsVILLAMAR, M; FERNANDEZ, E; AYUSO, C et al.Annales de génétique (Paris). 1990, Vol 33, Num 1, pp 29-31, issn 0003-3995Article

Uniparental disomy of chromosome 13q causing homozygosity for the 35delG mutation in the gene encoding connexin26 (GJB2) results in prelingual hearing impairment in two unrelated Spanish patientsALVAREZ, A; DEL CASTILLO, I; PERA, A et al.Journal of medical genetics. 2003, Vol 40, Num 8, pp 636-639, issn 0022-2593, 4 p.Article

A novel locus for non-syndromic sensorineural deafness (DFN6) maps to chromosome Xp22DEL CASTILLO, I; VILLAMAR, M; TAPIA, M. C et al.Human molecular genetics (Print). 1996, Vol 5, Num 9, pp 1383-1387, issn 0964-6906Article

The A1555G mutation in the 12S rRNA gene of human mtDNA: Recurrent origins and founder events in families affected by sensorineural deafnessTORRONI, A; CRUCIANI, F; VILLAMAR, M et al.American journal of human genetics. 1999, Vol 65, Num 5, pp 1349-1358, issn 0002-9297Article

A novel deletion involving the connexin-30 gene, del(GJb6-d13s1854), found in frans with mutations in the GJB2 gene (connexin-26) in subjects with DFNB1 non-syndromic hearing impairmentDEL CASTILLO, F. J; RODRIGUEZ-BALLESTEROS, M; PANDYA, A et al.Journal of medical genetics. 2005, Vol 42, Num 7, pp 588-594, issn 0022-2593, 7 p.Article