Differences in Leaf Morphological Parameters of Pear (<i>Pyrus communis</i> L.) Based on Their Susceptibility to European Pear Rust Caused by <i>Gymnosporangium sabinae</i> (Dicks....

by Katrīna Kārkliņa, Gunārs Lācis, Baiba Lāce
Published 2021-05-01

Presentation of Complex Homozygous Allele in ABCA4 Gene in a Patient with Retinitis Pigmentosa

by Māreta Audere, Katrīna Rutka, Svetlana Šepetiene, Baiba Lāce
Published 2015-01-01

Whole-exome sequencing identifies homozygous mutation in TTI2 in a child with primary microcephaly: a case report

by Vincent Picher-Martel, Yvan Labrie, Serge Rivest, Baiba Lace, Nicolas Chrestian
Published 2020-02-01

Genetic linkage studies of a North Carolina macular dystrophy family

by Mareta Audere, Katrina Rutka, Inna Inaskina, Raitis Peculis, Svetlana Sepetiene, Sandra Valeina, Baiba Lāce
Published 2016-01-01

Dupuytren's Contracture Cosegregation with Limb-Girdle Muscle Dystrophy

by Baiba Lace, Inna Inashkina, Ieva Micule, Inta Vasiljeva, Maruta Solvita Naudina, Jurgis Strautmanis, Janis Stavusis, Eriks Jankevics
Published 2013-01-01

A Homozygous Deep Intronic Mutation Alters the Splicing of Nebulin Gene in a Patient With Nemaline Myopathy

by Nathalie Laflamme, Baiba Lace, Samarth Thonta Setty, Nadie Rioux, Yvan Labrie, Arnaud Droit, Nicolas Chrestian, Serge Rivest
Published 2021-06-01

HSD10 mitochondrial disease: p.Leu122Val variant, mild clinical phenotype, and founder effect in French‐Canadian patients from Quebec

by Paula J. Waters, Baiba Lace, Daniela Buhas, Serge Gravel, Denis Cyr, Renée‐Myriam Boucher, Geneviève Bernard, Sébastien Lévesque, Bruno Maranda
Published 2019-12-01

A founder mutation in the PLPBP gene in families from Saguenay‐Lac‐St‐Jean region affected by a pyridoxine‐dependent epilepsy

by Maitou Pal, Baiba Lace, Yvan Labrie, Nathalie Laflamme, Nadie Rioux, Samarth Thonta Setty, Marc‐Andre Dugas, Louise Gosselin, Arnaud Droit, Nicolas Chrestian, Serge Rivest
Published 2021-05-01

Human Mitochondrial HMG-CoA Synthase Deficiency: Role of Enzyme Dimerization Surface and Characterization of Three New Patients

by Beatriz Puisac, Iñigo Marcos-Alcalde, María Hernández-Marcos, Pilar Tobajas Morlana, Alina Levtova, Bernd C. Schwahn, Corinne DeLaet, Baiba Lace, Paulino Gómez-Puertas, Juan Pié
Published 2018-03-01

Duplication events downstream of IRX1 cause North Carolina macular dystrophy at the MCDR3 locus

by Valentina Cipriani, Raquel S. Silva, Gavin Arno, Nikolas Pontikos, Ambreen Kalhoro, Sandra Valeina, Inna Inashkina, Mareta Audere, Katrina Rutka, Bernard Puech, Michel Michaelides, Veronica van Heyningen, Baiba Lace, Andrew R. Webster, Anthony T. Moore
Published 2017-08-01

Interaction between IRF6 and TGFA genes contribute to the risk of nonsyndromic cleft lip/palate.

by Ariadne Letra, Walid Fakhouri, Renata F Fonseca, Renato Menezes, Inga Kempa, Joanne L Prasad, Toby G McHenry, Andrew C Lidral, Lina Moreno, Jeffrey C Murray, Sandra Daack-Hirsch, Mary L Marazita, Eduardo E Castilla, Baiba Lace, Ieda M Orioli, Jose M Granjeiro, Brian C Schutte, Alexandre R Vieira
Published 2012-01-01