Search Results - Guilbride, Dorothy Lys

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  1. 1
    De Novo ACTG1 Variant Expands the Phenotype and Genotype of Partial Deafness and Baraitser-Winter Syndrome

    De Novo ACTG1 Variant Expands the Phenotype and Genotype of Partial Deafness and Baraitser-Winter Syndrome by Dawidziuk, Mateusz, Kutkowska-Kazmierczak, Anna, Bukowska-Olech, Ewelina, Jurek, Marta, Kalka, Ewa, Guilbride, Dorothy Lys, Furmanek, Mariusz Ireneusz, Bekiesinska-Figatowska, Monika, Bal, Jerzy, Gawlinski, Pawel

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  2. 2
    Congenital coenzyme Q5-linked pathology: causal genetic association, core phenotype, and molecular mechanism

    Congenital coenzyme Q5-linked pathology: causal genetic association, core phenotype, and molecular mechanism by Dawidziuk, Mateusz, Podwysocka, Aleksandra, Jurek, Marta, Obersztyn, Ewa, Bekiesinska-Figatowska, Monika, Goszczanska-Ciuchta, Alicja, Bukowska-Olech, Ewelina, Rygiel, Agnieszka Magdalena, Guilbride, Dorothy Lys, Wiszniewski, Wojciech, Gawlinski, Pawel

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  3. 3
    A Zebrafish/Drosophila Dual System Model for Investigating Human Microcephaly

    A Zebrafish/Drosophila Dual System Model for Investigating Human Microcephaly by Bartoszewski, Slawomir, Dawidziuk, Mateusz, Kasica, Natalia, Durak, Roma, Jurek, Marta, Podwysocka, Aleksandra, Guilbride, Dorothy Lys, Podlasz, Piotr, Winata, Cecilia Lanny, Gawlinski, Pawel

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  4. 4
    De Novo ACTG1 Variant Expands the Phenotype and Genotype of Partial Deafness and Baraitser-Winter Syndrome

    De Novo ACTG1 Variant Expands the Phenotype and Genotype of Partial Deafness and Baraitser-Winter Syndrome by Dawidziuk, Mateusz, Kutkowska-Kazmierczak, Anna, Bukowska-Olech, Ewelina, Jurek, Marta, Kalka, Ewa, Guilbride, Dorothy Lys, Furmanek, Mariusz Ireneusz, Bekiesinska-Figatowska, Monika, Bal, Jerzy, Gawlinski, Pawel

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