Un programa de genética en un país en desarrollo: Cuba = Cmoprehensive national genetic program in a developing country: CubaHEREDERO, L.Boletín de la Oficina sanitaria panamericana. 1993, Vol 115, Num 1, pp 32-38, issn 0030-0632Article

A NEW FORM OF THE SOLUBILITY TEST FOR HEMOGLOBIN S., RESULTS FROM A SURVEY OF 3000 CASES.HEREDERO L; GRANDA H; DORTICOS A et al.1976; CLIN. CHIM. ACTA; PAYS-BAS; DA. 1976; VOL. 71; NO 3; PP. 515-519; BIBL. 12 REF.Article

HAEMOGLOBIN PORTO ALEGRE IN A CUBAN FAMILY.MARTINEZ G; LIMA F; WADE M et al.1977; J. MED. GENET.; G.B.; DA. 1977; VOL. 14; NO 6; PP. 422-425; BIBL. 21 REF.Article

Aspectos eticos en genetica medica en Cuba = Ethical aspects on medical genetics in CubaROJAS, I; PENCHASZADEH, V; HEREDERO, L et al.Revista cubana de pediatría. 1993, Vol 65, Num 1, pp 57-63, issn 0034-7531Article

Aspectos éticos en genética médica en CubaROJAS, I; PENCHASZADEH, V; HEREDERO, L et al.REVISTA CUBANA DE PEDIATRIA. 1993, Num 1, pp 57-63Article

Aspectos éticos en genética médica en CubaROJAS, I; PENCHASZADEH, V; HEREDERO, L et al.REVISTA CUBANA DE PEDIATRIA. 1993, Num 1, pp 57-63Article

Diagnostico precoz de fenilcetonuria en Cuba (Informe preliminar) = Diagnostic précoce de phénylcétonurie à Cuba = Early diagnosis of phenylketonuria in CubaHEREDERO, L; ATENCIO, G; VEGA, J. L et al.Revista cubana de pediatría. 1987, Vol 58, Num 1, pp 27-33, issn 0034-7531Article

Results of 12 years' combined maternal serum alpha-fetoprotein screening and ultrasound fetal monitoring for prenatal detection of fetal malformations in Havana City, CubaRODRIGUEZ, L; SANCHEZ, R; HERNANDEZ, J et al.Prenatal diagnosis. 1997, Vol 17, Num 4, pp 301-304, issn 0197-3851Article

Diagnostico prenatal de la fibrosis quistica en Cuba = Diagnostic anténatal de la mucoviscidose à Cuba = Prenatal diagnosis of cystis fibrosis in CubaDAVILA, L; RODRIGUEZ, L; ZALDIVAR, O et al.Revista cubana de pediatría. 1989, Vol 61, Num 1, pp 134-142, issn 0034-7531Article

Frequency of Delta-F508 mutation and XV2C/KM19 haplotypes in Cuban cystic fibrosis familiesCOLLAZO, T; MAGARINO, C; CHAVEZ, R et al.Human heredity. 1995, Vol 45, Num 1, pp 55-57, issn 0001-5652Article

Genetic mapping of the spinocerebellar ataxia 2 (SCA2) locus on chromosome 12q23-q24.1HERNANDEZ, A; MAGARINO, C; GISPERT, S et al.Genomics (San Diego, Calif.). 1995, Vol 25, Num 2, pp 433-435, issn 0888-7543Article

Results from a reference laboratory for prenatal diagnosis of sickle cell disorders in CubaGRANDA, H; GISPERT, S; MARTINEZ, G et al.Prenatal diagnosis. 1994, Vol 14, Num 8, pp 659-662, issn 0197-3851Article

Maternal serum alpha-fetoprotein screening for neural tube defects and other disorders using ultramicro-ELISA: collaborative study in Cuba and in the German Democratic RepublicKÖPRNER, H; RODRIGUEZ, L; SOLIS, R et al.Human genetics. 1986, Vol 73, Num 1, pp 60-63, issn 0340-6717Article

Cuban programme for prevention of sickle cell diseaseGRANDA, H; GISPERT, S; DORTICOS, A et al.Lancet (British edition). 1991, Vol 337, Num 8734, pp 152-153, issn 0140-6736, 2 p.Article