18p Deletion Syndrome With a 45, XY, t (14;18) (p11.1; p11.1), Karyotype von Ashgan, Baraah, Al-Agha, Abdulmoein, Alhamdani, Yara, Shazly, Mohamed Abdelmaksoud

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Precocious Puberty Associated with Testicular Hormone-secreting Leydig Cell Tumor von Alagha, Eid, Kafi, Shahd E, Shazly, Mohamed Abdelmaksoud, Al-Agha, Abdulmoein

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Pseudo-precocious Puberty Associated with an Adrenocortical Tumor in a Young Child von Kafi, Shahd E, Alagha, Eid, Shazly, Mohamed Abdelmaksoud, Al-Agha, Abdulmoein

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Classical 11β-Hydroxylase Deficiency Caused by a Novel Homozygous Mutation: A Case Study and Literature Review von Alsanea, Mohammad N, Al-Agha, Abdulmoein, Shazly, Mohamed Abdelmaksoud

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18p Deletion Syndrome With a 45, XY, t (14;18) (p11.1; p11.1), Karyotype von Ashgan, Baraah, Al-Agha, Abdulmoein, Alhamdani, Yara, Shazly, Mohamed Abdelmaksoud

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Classical 11β-Hydroxylase Deficiency Caused by a Novel Homozygous Mutation: A Case Study and Literature Review von Alsanea, Mohammad N, Al-Agha, Abdulmoein, Shazly, Mohamed Abdelmaksoud

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Pseudo-precocious Puberty Associated with an Adrenocortical Tumor in a Young Child von Kafi, Shahd E, Alagha, Eid, Shazly, Mohamed Abdelmaksoud, Al-Agha, Abdulmoein

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Precocious Puberty Associated with Testicular Hormone-secreting Leydig Cell Tumor von Alagha, Eid, Kafi, Shahd E, Shazly, Mohamed Abdelmaksoud, Al-Agha, Abdulmoein

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