Absence of EIF1AX, PPM1D, and CHEK2 mutations reported in Thyroid Cancer Genome Atlas (TCGA) in a large series of thyroid cancer
Alzahrani, Ali S., Murugan, Avaniyapuram Kannan, Qasem, Ebtesam, Alswailem, Meshael M., AlGhamdi, Balgees, Moria, Yosra, Al-Hindi, Hindi
Published in Endocrine (01.01.2019)
Published in Endocrine (01.01.2019)
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Journal Article
Mutational analysis of rare subtypes of congenital adrenal hyperplasia in a highly inbred population
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.
Published in Molecular and cellular endocrinology (05.02.2018)
Published in Molecular and cellular endocrinology (05.02.2018)
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Journal Article
Molecular genetics and phenotype/genotype correlation of 5-α reductase deficiency in a highly consanguineous population
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.
Published in Endocrine (01.02.2019)
Published in Endocrine (01.02.2019)
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Journal Article
Correction to: Absence of EIF1AX, PPM1D, and CHEK2 mutations reported in Thyroid Cancer Genome Atlas (TCGA) in a large series of thyroid cancer
Alzahrani, Ali S., Murugan, Avaniyapuram Kannan, Qasem, Ebtesam, Alswailem, Meshael M., AlGhamdi, Balgees, Moria, Yosra, Al-Hindi, Hindi
Published in Endocrine (01.07.2019)
Published in Endocrine (01.07.2019)
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Journal Article
A high rate of novel CYP11B1 mutations in Saudi Arabia
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
Published in The Journal of steroid biochemistry and molecular biology (01.11.2017)
Published in The Journal of steroid biochemistry and molecular biology (01.11.2017)
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