Search Results - Al‐Obaidi, Ruqayah G. Y.

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  1. 1
    Epigenomic and phenotypic characterization of DEGCAGS syndrome

    Epigenomic and phenotypic characterization of DEGCAGS syndrome by Karimi, Karim, Weis, Denisa, Aukrust, Ingvild, Hsieh, Tzung-Chien, Horackova, Marie, Paulsen, Julie, Mendoza Londono, Roberto, Dupuis, Lucie, Dickson, Megan, Lesman, Hellen, Lau, Tracy, Murphy, David, Hama Salih, Khalid, Al-Musawi, Bassam M. S., Al-Obaidi, Ruqayah G. Y., Rydzanicz, Malgorzata, Biela, Mateus, Santos, Mafalda Saraiva, Aldeeri, Abdulrahman, Gazda, Hanna T., Pais, Lynn, Shril, Shirlee, Døllner, Henrik, Bartakke, Sandip, Laccone, Franco, Soltysova, Andrea, Kitzler, Thomas, Soliman, Neveen A., Relator, Raissa, Levy, Michael A., Kerkhof, Jennifer, Rzasa, Jessica, Houlden, Henry, Pilshofer, Gabriela V., Jobst-Schwan, Tilman, Hildebrandt, Friedhelm, Sousa, Sergio B., Maroofian, Reza, Yu, Timothy W., Krawitz, Peter, Sadikovic, Bekim, Douzgou Houge, Sofia

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  2. 2
    Molecular Analysis of CYP21A2 Gene Mutations among Iraqi Patients with Congenital Adrenal Hyperplasia

    Molecular Analysis of CYP21A2 Gene Mutations among Iraqi Patients with Congenital Adrenal Hyperplasia by Al-Obaidi, Ruqayah G. Y., Al-Musawi, Bassam M. S., Al-Zubaidi, Munib Ahmed K., Oberkanins, Christian, Németh, Stefan, Al-Obaidi, Yusra G. Y.

    Published in Enzyme Research
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  3. 3
    Primary hypogonadism, partial alopecia, and Müllerian hypoplasia: report of a fifth family and review

    Primary hypogonadism, partial alopecia, and Müllerian hypoplasia: report of a fifth family and review by Al‐Obaidi, Ruqayah G. Y., Al‐Musawi, Bassam M. S.

    Published in Clinical case reports
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  4. 4
    Primary hypogonadism, partial alopecia, and Müllerian hypoplasia: report of a fifth family and review

    Primary hypogonadism, partial alopecia, and Müllerian hypoplasia: report of a fifth family and review by Al-Obaidi, Ruqayah G Y, Al-Musawi, Bassam M S

    Published in Clinical case reports
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