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Orlova E.M.

FGU Éndokrinologicheskiĭ nauchnyĭ tsentr Minzdravsotsrazvitiia Rossiĭskoĭ Federatsii, Moskva

Kurkina M.V.

Research Center for Medical Genetics, Moscow, Russia

Sozaeva L.S.

FGBU "Éndokrinologicheskiĭ nauchnyĭ tsentr" Minzdrava RF, Moskva

Kareva M.A.

Institut detskoĭ éndokrinologii Éndokrinologicheskogo nauchnogo tsentra, Moskva

Kanivets I.V.

Research Center for Medical Genetics «Genomed», Moscow, Russia

Antonets A.V.

Research Center for Medical Genetics «Genomed», Moscow, Russia

Zakharova E.Iu.

Mediko-geneticheskiĭ tsentr RAMN

A case report of concomitant myopathy, adrenal insufficiency, and mental retardation linked with deletion of Xp21

Authors:

Orlova E.M., Kurkina M.V., Sozaeva L.S., Kareva M.A., Kanivets I.V., Antonets A.V., Zakharova E.Iu.

More about the authors

Journal: Problems of Endocrinology. 2017;63(5): 329‑333

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To cite this article:

Orlova EM, Kurkina MV, Sozaeva LS, Kareva MA, Kanivets IV, Antonets AV, Zakharova EIu. A case report of concomitant myopathy, adrenal insufficiency, and mental retardation linked with deletion of Xp21. Problems of Endocrinology. 2017;63(5):329‑333. (In Russ.)
https://doi.org/10.14341/probl2017635329-333

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