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Delta Like-1 Gene Mutation: A Novel Cause of Congenital Vertebral Malformation. [electronic resource] by
- Barhoumi, Tlili
- Nashabat, Marwan
- Alghanem, Bandar
- Alhallaj, AlShaimaa
- Boudjelal, Mohamed
- Umair, Muhammad
- Alarifi, Saud
- Alfares, Ahmed
- Mohrij, Saad A Al
- Alfadhel, Majid
Publication details: Frontiers in genetics 2019
In:
Frontiers in genetics vol. 10
Availability: No items available.
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686.
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687.
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688.
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689.
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690.
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Head and neck neuroendocrine tumors at a single institution over 15 years. [electronic resource] by
- Bacalao, Maria
- Beg, Muhammad S
- Cavuoti, Dominick
- Zhu, Hong
- Sumer, Baran
- Myers, Larry
- Truelson, John
- Nedzi, Lucien
- Sher, David
- Hughes, Randall
- Khan, Saad A
Publication details: Clinical case reports Dec 2019
In:
Clinical case reports vol. 7
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Functional evidence implicating FOXL2 in non-syndromic premature ovarian failure and in the regulation of the transcription factor OSR2. [electronic resource] by
- Laissue, P
- Lakhal, B
- Benayoun, B A
- Dipietromaria, A
- Braham, R
- Elghezal, H
- Philibert, P
- Saâd, A
- Sultan, C
- Fellous, M
- Veitia, R A
Producer: 20090923
In:
Journal of medical genetics vol. 46
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699.
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700.
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