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Founder mutation for Huntington disease in Caucasus Jews. [electronic resource] by
- Melamed, O
- Behar, D M
- Bram, C
- Magal, N
- Pras, E
- Reznik-Wolf, H
- Borochowitz, Z U
- Davidov, B
- Mor-Cohen, R
- Baris, H N
Producer: 20150916
In:
Clinical genetics vol. 87
Availability: No items available.
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Novel WWOX deleterious variants cause early infantile epileptic encephalopathy, severe developmental delay and dysmorphism among Yemenite Jews. [electronic resource] by
- Weisz-Hubshman, M
- Meirson, H
- Michaelson-Cohen, R
- Beeri, R
- Tzur, S
- Bormans, C
- Modai, S
- Shomron, N
- Shilon, Y
- Banne, E
- Orenstein, N
- Konen, O
- Marek-Yagel, D
- Veber, A
- Shalva, N
- Imagawa, E
- Matsumoto, N
- Lev, D
- Lerman Sagie, T
- Raas-Rothschild, A
- Ben-Zeev, B
- Basel-Salmon, L
- Behar, D M
- Heimer, G
Producer: 20190722
In:
European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society vol. 23
Availability: No items available.
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