Showing 1 - 4 results of 4 for search 'Kadri Karaer', query time: 0.01s Refine Results
  1. 1
    A novel mutation in a case of pseudohypoparathyroidism type Ia

    A novel mutation in a case of pseudohypoparathyroidism type Ia by Birgül Kırel, Meliha Demiral, Özkan Bozdağ, Kadri Karaer

    Published 2016-02-01
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  2. 2
    Microcephaly and developmental delay caused by short-chain acyl-CoA dehydrogenase deficiency

    Microcephaly and developmental delay caused by short-chain acyl-CoA dehydrogenase deficiency by Mustafa Kılıç, Saliha Şenel, Kadri Karaer, Serdar Ceylaner

    Published 2017-12-01
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  3. 3
    A case with a ring chromosome 22

    A case with a ring chromosome 22 by Altuğ Koç, Kadri Karaer, Mehmet Ali Ergün, Meral Yirmibeş-Karaoğuz, Derya Kan, Ali Cansu, Ferda Perçin

    Published 2008-04-01
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  4. 4
    Two newborn babies with generalized arterial calcification of infancy, two new mutations

    Two newborn babies with generalized arterial calcification of infancy, two new mutations by Hacer Yapıcıoğlu-Yıldızdaş, Nazan Özbarlas, Sevcan Erdem, Mehmet Bertan Yılmaz, Ferda Özlü, Selim Büyükkurt, Süreyya Soyupak, Utku Güllü, Kadri Karaer

    Published 2016-08-01
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