Showing 1 - 5 results of 5 for search 'Latos-Bielenska Anna', query time: 0.03s Refine Results
  1. 1
    Isolated brachydactyly type E caused by a <it>HOXD13 </it>nonsense mutation: a case report

    Isolated brachydactyly type E caused by a <it>HOXD13 </it>nonsense mutation: a case report by Jamsheer Aleksander, Sowińska Anna, Kaczmarek Leszek, Latos-Bieleńska Anna

    Published 2012
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  2. 2
    Bilateral radial agenesis with absent thumbs, complex heart defect, short stature, and facial dysmorphism in a patient with pure distal microduplication of 5q35.2-5q35.3

    Bilateral radial agenesis with absent thumbs, complex heart defect, short stature, and facial dysmorphism in a patient with pure distal microduplication of 5q35.2-5q35.3 by Jamsheer Aleksander, Sowińska Anna, Simon Dorota, Jamsheer-Bratkowska Małgorzata, Trzeciak Tomasz, Latos-Bieleńska Anna

    Published 2013
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  3. 3
    Osteopoikilosis and multiple exostoses caused by novel mutations in <it>LEMD3 </it>and <it>EXT1 </it>genes respectively - coincidence within one family

    Osteopoikilosis and multiple exostoses caused by novel mutations in <it>LEMD3 </it>and <it>EXT1 </it>genes respectively - coincidence within one family by Horn Denise, Kolanczyk Mateusz, Jamsheer Aleksander, Baasanjav Sevjidmaa, Latos Tomasz, Hoffmann Katrin, Latos-Bielenska Anna, Mundlos Stefan

    Published 2010
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  4. 4
    Exploring Research Priorities of Parents Who Have Children With Down Syndrome, Cleft Lip With or Without Cleft Palate, Congenital Heart Defects, or Spina Bifida Using ConnectEpeople: A Social Media Coproduction Research Study

    Exploring Research Priorities of Parents Who Have Children With Down Syndrome, Cleft Lip With or Without Cleft Palate, Congenital Heart Defects, or Spina Bifida Using ConnectEpeopl... by Sinclair, Marlene, McCullough, Julie EM, Elliott, David, Latos-Bielenska, Anna, Braz, Paula, Cavero-Carbonell, Clara, Jamry-Dziurla, Anna, João Santos, Ana, Páramo-Rodríguez, Lucía

    Published 2019
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  5. 5
    Frequency of 22q11.2 microdeletion in children with congenital heart defects in western poland

    Frequency of 22q11.2 microdeletion in children with congenital heart defects in western poland by Zeyland Joanna, Krawczynski Maciej R, Skolozdrzy Joanna, Badura-Stronka Magdalena, Moszura Tomasz, Materna-Kiryluk Anna, Glazar Renata, Wisniewska Marzena, Wolnik-Brzozowska Danuta, Wozniak Anna, Bobkowski Waldemar, Slomski Ryszard, Latos-Bielenska Anna, Siwinska Aldona

    Published 2010
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