Works matching IS 13085727 AND DT 2021 AND VI 13 AND IP 1


Results: 15
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    6q25.1-q25.3 Microdeletion in a Chinese Girl.

    Published in:
    Journal of Clinical Research in Pediatric Endocrinology, 2021, v. 13, n. 1, p. 109, doi. 10.4274/jcrpe.galenos.2020.2020.0008
    By:
    • Mian-Ling Zhong;
    • Ye-Mei Song;
    • Chao-Chun Zou
    Publication type:
    Article
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    A New Cause of Obesity Syndrome Associated with a Mutation in the Carboxypeptidase Gene Detected in Three Siblings with Obesity, Intellectual Disability and Hypogonadotropic Hypogonadism.

    Published in:
    Journal of Clinical Research in Pediatric Endocrinology, 2021, v. 13, n. 1, p. 52, doi. 10.4274/jcrpe.galenos.2020.2020.0101
    By:
    • Durmaz, Asude;
    • Aykut, Ayça;
    • Atik, Tahir;
    • Özen, Samim;
    • Emecen, Durdugül Ayyıldız;
    • Ata, Aysun;
    • Işık, Esra;
    • Gökşen, Damla;
    • Çoğulu, Özgür;
    • Özkınay, Ferda
    Publication type:
    Article
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    Identification of Three Novel and One Known Mutation in the WFS1 Gene in Four Unrelated Turkish Families: The Role of Homozygosity Mapping in the Early Diagnosis.

    Published in:
    Journal of Clinical Research in Pediatric Endocrinology, 2021, v. 13, n. 1, p. 34, doi. 10.4274/jcrpe.galenos.2020.2020.0152
    By:
    • Sherif, Maha;
    • Demirbilek, Hüseyin;
    • Çayır, Atilla;
    • Tahir, Sophia;
    • Çavdarlı, Büşra;
    • Demiral, Meliha;
    • Cebeci, Ayşe Nurcan;
    • Vurallı, Doğuş;
    • Rahman, Sofia Asim;
    • Unal, Edip;
    • Büyükyılmaz, Gönül;
    • Baran, Rıza Taner;
    • Özbek, Mehmet Nuri;
    • Hussain, Khalid
    Publication type:
    Article
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