Association between minihaplotypes and mutations at the phenylalanine hydroxylase locus in Latvian phenylketonuria patients

by Proņina Natālija, Lugovska Rita
Published 2011-01-01

The fragile X syndrome: 13 years of experience

by Daneberga Zanda, Krūmiņa Zita, Lāce Baiba, Bauze Daiga, Lugovska Rita
Published 2011-01-01

Fragile X Syndrome in Mentally Retarded Patients from Latvia

by Daneberga Zanda, Krūmiņa Zita, Lāce Baiba, Bauze Daiga, Proņina Natālija, Lugovska Rita
Published 2009-01-01

Spectrum and Frequency of the GJB2 Gene Mutations Among Latvian Patients with Prelingual Nonsyndromic Hearing Loss

by Šterna Olga, Proņina Natālija, Grīnfelde Ieva, Kušķe Sandra, Krūmiņa Astrīda, Lugovska Rita, Pētersons Aigars
Published 2009-01-01

Neonatal Cystic Fibrosis Screening in Latvia: A Pilot Project

by Lāce Baiba, Grīnblate Santa, Korņejeva Liene, Švābe Vija, Grauduma Ineta, Vēvere Pārsla, Lugovska Rita, Krams Alvils, Martinsons Agris
Published 2009-01-01