Search Results - Tuc Bengur, Ecenur

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  1. 1
    Impact of deep phenotyping: high diagnostic yield in a diverse pediatric population of 172 patients through clinical whole-genome sequencing at a single center

    Impact of deep phenotyping: high diagnostic yield in a diverse pediatric population of 172 patients through clinical whole-genome sequencing at a single center by Akgun-Dogan, Ozlem, Tuc Bengur, Ecenur, Ay, Beril, Ozkose, Gulsah Sebnem, Kar, Emre, Bengur, Fuat Baris, Bulut, Aybike S, Yigit, Ayca, Aydin, Eylul, Esen, Fatma Nisa, Ozdemir, Ozkan, Yesilyurt, Ahmet, Alanay, Yasemin

    Published in Frontiers in genetics
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  2. 2
    Infantile Krabbe disease (0–12 months), progression, and recommended endpoints for clinical trials

    Infantile Krabbe disease (0–12 months), progression, and recommended endpoints for clinical trials by Greco, Melissa R., Lopez, Mabel A., Beltran‐Quintero, Maria L., Tuc Bengur, Ecenur, Poe, Michele D., Escolar, Maria L.

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  3. 3
    P371: Alternative diagnoses of PHACES syndrome with overlapping features

    P371: Alternative diagnoses of PHACES syndrome with overlapping features by Bengur, Ecenur Tuc, Shmuylovich, Leo, Menezes, Maithilee, King, Katherine

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  4. 4
    Genetics and Primary Care: Raising Awareness and Enhancing Cooperation

    Genetics and Primary Care: Raising Awareness and Enhancing Cooperation by Bengur, Ecenur Tuc, Heeley, Jennifer

    Published in Missouri medicine
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  5. 5
    Psychosine predicts age of onset in babies with Krabbe disease

    Psychosine predicts age of onset in babies with Krabbe disease by Bengur, Ecenur Tuc, Halthore, Amitha, Poe, Michele D., Escolar, Maria L.

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  6. 6
    The third family with TAF6‐related phenotype: Alazami‐Yuan syndrome

    The third family with TAF6‐related phenotype: Alazami‐Yuan syndrome by Tuc, Ecenur, Bengur, Fuat Baris, Aykut, Aslan, Sahin, Ozlem, Alanay, Yasemin

    Published in Clinical genetics
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  7. 7
    The third family with TAF6-related phenotype: Alazami-Yuan syndrome

    The third family with TAF6-related phenotype: Alazami-Yuan syndrome by Tuc, Ecenur, Bengur, Fuat Baris, Aykut, Aslan, Sahin, Ozlem, Alanay, Yasemin

    Published in Clinical genetics
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