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38201.
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38202.
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38203.
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38204.
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38205.
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38206.
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38207.
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Mutations in TMEM260 Cause a Pediatric Neurodevelopmental, Cardiac, and Renal Syndrome. [electronic resource] by
- Ta-Shma, Asaf
- Khan, Tahir N
- Vivante, Asaf
- Willer, Jason R
- Matak, Pavle
- Jalas, Chaim
- Pode-Shakked, Ben
- Salem, Yishay
- Anikster, Yair
- Hildebrandt, Friedhelm
- Katsanis, Nicholas
- Elpeleg, Orly
- Davis, Erica E
Producer: 20170426
In:
American journal of human genetics vol. 100
Availability: No items available.
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38208.
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Loss-of-Function Mutations in LGI4, a Secreted Ligand Involved in Schwann Cell Myelination, Are Responsible for Arthrogryposis Multiplex Congenita. [electronic resource] by
- Xue, Shifeng
- Maluenda, Jérôme
- Marguet, Florent
- Shboul, Mohammad
- Quevarec, Loïc
- Bonnard, Carine
- Ng, Alvin Yu Jin
- Tohari, Sumanty
- Tan, Thong Teck
- Kong, Mung Kei
- Monaghan, Kristin G
- Cho, Megan T
- Siskind, Carly E
- Sampson, Jacinda B
- Rocha, Carolina Tesi
- Alkazaleh, Fawaz
- Gonzales, Marie
- Rigonnot, Luc
- Whalen, Sandra
- Gut, Marta
- Gut, Ivo
- Bucourt, Martine
- Venkatesh, Byrappa
- Laquerrière, Annie
- Reversade, Bruno
- Melki, Judith
Producer: 20170426
In:
American journal of human genetics vol. 100
Availability: No items available.
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38209.
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Experimental and theoretical evidence for the ferromagnetic edge in WSe [electronic resource] by
- Tao, Lei
- Meng, Fanchen
- Zhao, Shudong
- Song, Yongli
- Yu, Jianxin
- Wang, Xianjie
- Liu, Zhiguo
- Wang, Yi
- Li, Bingsheng
- Wang, Yang
- Sui, Yu
Producer: 20180718
In:
Nanoscale vol. 9
Availability: No items available.
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38210.
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38211.
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38212.
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38213.
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38214.
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38215.
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38216.
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38217.
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38218.
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38219.
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38220.
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