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17981.
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17982.
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17990.
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17991.
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17992.
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17993.
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17994.
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17995.
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17996.
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Mutations in SMG9, Encoding an Essential Component of Nonsense-Mediated Decay Machinery, Cause a Multiple Congenital Anomaly Syndrome in Humans and Mice. [electronic resource] by
- Shaheen, Ranad
- Anazi, Shams
- Ben-Omran, Tawfeg
- Seidahmed, Mohammed Zain
- Caddle, L Brianna
- Palmer, Kristina
- Ali, Rehab
- Alshidi, Tarfa
- Hagos, Samya
- Goodwin, Leslie
- Hashem, Mais
- Wakil, Salma M
- Abouelhoda, Mohamed
- Colak, Dilek
- Murray, Stephen A
- Alkuraya, Fowzan S
Producer: 20160829
In:
American journal of human genetics vol. 98
Availability: No items available.
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17997.
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Sequencing the GRHL3 Coding Region Reveals Rare Truncating Mutations and a Common Susceptibility Variant for Nonsyndromic Cleft Palate. [electronic resource] by
- Mangold, Elisabeth
- Böhmer, Anne C
- Ishorst, Nina
- Hoebel, Ann-Kathrin
- Gültepe, Pinar
- Schuenke, Hannah
- Klamt, Johanna
- Hofmann, Andrea
- Gölz, Lina
- Raff, Ruth
- Tessmann, Peter
- Nowak, Stefanie
- Reutter, Heiko
- Hemprich, Alexander
- Kreusch, Thomas
- Kramer, Franz-Josef
- Braumann, Bert
- Reich, Rudolf
- Schmidt, Gül
- Jäger, Andreas
- Reiter, Rudolf
- Brosch, Sibylle
- Stavusis, Janis
- Ishida, Miho
- Seselgyte, Rimante
- Moore, Gudrun E
- Nöthen, Markus M
- Borck, Guntram
- Aldhorae, Khalid A
- Lace, Baiba
- Stanier, Philip
- Knapp, Michael
- Ludwig, Kerstin U
Producer: 20160829
In:
American journal of human genetics vol. 98
Availability: No items available.
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17998.
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17999.
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18000.
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