Absence of EIF1AX, PPM1D, and CHEK2 mutations reported in Thyroid Cancer Genome Atlas (TCGA) in a large series of thyroid cancer von Alzahrani, Ali S., Murugan, Avaniyapuram Kannan, Qasem, Ebtesam, Alswailem, Meshael M., AlGhamdi, Balgees, Moria, Yosra, Al-Hindi, Hindi

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Mutational analysis of rare subtypes of congenital adrenal hyperplasia in a highly inbred population von Alswailem, Meshael M., Alzahrani, Ohoud S., Alhomaidah, Doha S., Alasmari, Rahma, Qasem, Ebtesam, Murugan, Avaniyapuram Kannan, Alsagheir, Afaf, Brema, Imad, Abbas, Bassam Ben, Almehthel, Mohammed, Almeqbali, Ali, Alzahrani, Ali S.

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Molecular genetics and phenotype/genotype correlation of 5-α reductase deficiency in a highly consanguineous population von Alswailem, Meshael M., Alzahrani, Ohoud S., Alghofaili, Lamyaa, Qasem, Ebtesam, Almohanaa, Mai, Alsagheir, Afaf, Bin Abbas, Bassam, Attia, Najya A., Al Shaikh, Adnan, Alzahrani, Ali S.

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Correction to: Absence of EIF1AX, PPM1D, and CHEK2 mutations reported in Thyroid Cancer Genome Atlas (TCGA) in a large series of thyroid cancer von Alzahrani, Ali S., Murugan, Avaniyapuram Kannan, Qasem, Ebtesam, Alswailem, Meshael M., AlGhamdi, Balgees, Moria, Yosra, Al-Hindi, Hindi

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A high rate of novel CYP11B1 mutations in Saudi Arabia von Alzahrani, Ali S., Alswailem, Meshael M., Murugan, Avaniyapuram Kannan, Alhomaidah, Doha S., Capper, Cameron P., Auchus, Richard J., Qasem, Ebtesam, Alzahrani, Ohoud S., Al-Sagheir, Afaf, Bin-Abbas, Bassam

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Case Report: Severe Gonadal Dysgenesis Causing 46,XY Disorder of Sex Development Due to a Novel NR5A1 Variant von Alhamoudi, Kheloud M., Alghamdi, Balgees, Aljomaiah, Abeer, Alswailem, Meshael, Al-Hindi, Hindi, Alzahrani, Ali S.

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A CYP11A1 homozygous exonic variant inducing an alternative splicing, frameshift and truncation in a family with congenital adrenal hyperplasia von Alhamoudi, Kheloud M., Alswailem, Meshael, Alghamdi, Balgees, Alashwal, Abdullah, Alzahrani, Ali S.

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A Unique Mechanism of a Novel Synonymous PHEX Variant Causing X-Linked Hypophosphatemia von Alhamoudi, Kheloud M, Alghamdi, Balgees, Alswailem, Meshael, Nasir, Abdul, Aljomaiah, Abeer, Al-Hindi, Hindi, Alzahrani, Ali S

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Germline Variants in Sporadic Pituitary Adenomas von Alzahrani, Ali S, Bin Nafisah, Abdulghani, Alswailem, Meshael, Alghamdi, Balgees, Alsaihati, Burair, Aljafar, Hussain, Baz, Batoul, Alhindi, Hindi, Moria, Yosra, Butt, Muhammad Imran, Alkabbani, Abdulrahman Ghiatheddin, Alshaikh, Omalkhaire M, Alnassar, Anhar, Bin Afeef, Ahmed, AlQuraa, Reem, Alsuhaibani, Rawan, Alhadlaq, Omar, Abothenain, Fayha, Altwaijry, Yasser A

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LBMON174 Germline Molecular Genetics Of Pituitary Adenomas von Alzahrani, Ali, Nafisah, Abdulghani Bin, Alswailem, Meshael, Alsaihati, Burair, Alnassar, Anhar, Bin Afeef, Ahmed, AlQuraa, Reem, Alsuhaibani, Rawan, Alhadlaq, Omar, Altwaijry, Yasser A, Abothenain, Fayha, AlBaz, Batoul, Aljafar, Hussein, Moria, Yosra, Butt, Mohammad Imran, Alkabbani, Abdulrahman Ghiatheddin, Alshaikh, Omalkhaire M

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Case Report: Severe Gonadal Dysgenesis Causing 46,XY Disorder of Sex Development Due to a Novel NR5A1 Variant von Alhamoudi, Kheloud M, Alghamdi, Balgees, Aljomaiah, Abeer, Alswailem, Meshael, Al-Hindi, Hindi, Alzahrani, Ali S

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