The fragile X syndrome: 13 years of experience
Daneberga, Zanda, Krūmiņa, Zita, Lāce, Baiba, Bauze, Daiga, Lugovska, Rita
Spectrum and Frequency of the GJB2 Gene Mutations Among Latvian Patients with Prelingual Nonsyndromic Hearing Loss
Šterna, Olga, Proņina, Natālija, Grīnfelde, Ieva, Kušķe, Sandra, Krūmiņa, Astrīda, Lugovska, Rita, Pētersons, Aigars
Association between minihaplotypes and mutations at the phenylalanine hydroxylase locus in Latvian phenylketonuria patients
Proņina, Natālija, Lugovska, Rita
Fragile X Syndrome in Mentally Retarded Patients from Latvia
Daneberga, Zanda, Krūmiņa, Zita, Lāce, Baiba, Bauze, Daiga, Proņina, Natālija, Lugovska, Rita
Neonatal Cystic Fibrosis Screening in Latvia: A Pilot Project
Lāce, Baiba, Grīnblate, Santa, Korņejeva, Liene, Švābe, Vija, Grauduma, Ineta, Vēvere, Pārsla, Lugovska, Rita, Krams, Alvils, Martinsons, Agris