Mutations in MEOX1, Encoding Mesenchyme Homeobox 1, Cause Klippel-Feil Anomaly

المنشورات

مقال فى مجلة

2013

تم النشر فى:

Alkuraya, Jawahir Y. Mohamed, Eissa Faqeih, Abdulmonem Alsiddiky, Muneera J. Alshammari, Niema A. Ibrahim, and Fowzan S. . 2013

قراءة

نوع عمل المنشور

دكتوراة

رقم المجلد

رقم الانشاء

مجلة/صحيفة

The American Journal of Human genetics

الصفحات

175-161

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عبدالمنعم بن محمد الصديقي

Mutations in MEOX1, Encoding Mesenchyme Homeobox 1, Cause Klippel-Feil Anomaly

Alkuraya, Jawahir Y. Mohamed, Eissa Faqeih, Abdulmonem Alsiddiky, Muneera J. Alshammari, Niema A. Ibrahim, and Fowzan S. . 2013