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Ghadir Elias-Assad
Ghadir Elias-Assad
Medicine
Pediatrics
Mutation
Persistent Müllerian duct syndrome
Gene
5
Papers
1
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0
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High Prevalence of Hearing Impairment in Primary Congenital Hypothyroidism
2020
European thyroid journal
Tal Almagor
Shoshana Rath
Dan Nachtigal
Zohara Sharroni
Ghadir Elias-Assad
Ora Hess
Gilad Havazelet
Yoav Zehavi
Ronen Spiegel
Dani Bercovich
Shlomo Almashanu
Yardena Tenenbaum-Rakover
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The Evolving Role of Whole Exome Sequencing in the Diagnosis of Disorders of Sex Development (DSD)
2019
Yardena Tenenbaum-Rakover
Osnat Admoni
Ghadir Elias-Assad
Shira London
Barhoum Marie Noufi
Hana Ludar
Tal Almagor
Rita Bertalan
Anu Bashamboo
Ken McElreavey
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Hearing Loss Among Patients with Congenital Hypothyroidism
2018
Tal Almagor
Dan Nachtigal
Zohara Sharoni
Ghadir Elias-Assad
Ora Hess
Gilad Havazelet
Yardena Tenenbaum-Rakover
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Neonatal Diabetes Mellitus Caused by a Novel GLIS3 Mutation in Twins
2018
Shira London
Ghadir Elias-Assad
Marie Noufi Barhoum
Clari Felszer
Marina Paniakov
Scott Vainer
Sarah Flanagan
Jayne A. L. Houghton
Yardena Tenenbaum-Rakover
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A Novel Mutation of Anti-Mullerian Hormone Receptor Gene in a Male with Persistent Mullerian Duct Syndrome
2015
Ghadir Elias-Assad
Marwan Elias
Asher Pressman
Yardena Tenenbaum-Rakover
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