Results
|
|
1681.
|
|
|
|
1682.
|
|
|
|
1683.
|
|
|
|
1684.
|
|
|
|
1685.
|
|
|
|
1686.
|
|
|
|
1687.
|
|
|
|
1688.
|
|
|
|
1689.
|
|
|
|
1690.
|
Rare sequence variants in ANO3 and GNAL in a primary torsion dystonia series and controls. [electronic resource] by
- Zech, Michael
- Gross, Nadine
- Jochim, Angela
- Castrop, Florian
- Kaffe, Maria
- Dresel, Christian
- Lichtner, Peter
- Peters, Annette
- Gieger, Christian
- Meitinger, Thomas
- Haslinger, Bernhard
- Winkelmann, Juliane
Producer: 20140919
In:
Movement disorders : official journal of the Movement Disorder Society vol. 29
Availability: No items available.
|
|
|
1691.
|
|
|
|
1692.
|
|
|
|
1693.
|
|
|
|
1694.
|
|
|
|
1695.
|
|
|
|
1696.
|
Neonatal epileptic encephalopathy caused by de novo GNAO1 mutation misdiagnosed as atypical Rett syndrome: Cautions in interpretation of genomic test results. [electronic resource] by
- Gerald, Brittany
- Ramsey, Keri
- Belnap, Newell
- Szelinger, Szabolcs
- Siniard, Ashley L
- Balak, Chris
- Russell, Megan
- Richholt, Ryan
- De Both, Matt
- Claasen, Ana M
- Schrauwen, Isabelle
- Huentelman, Matthew J
- Craig, David W
- Rangasamy, Sampathkumar
- Narayanan, Vinodh
Producer: 20181127
In:
Seminars in pediatric neurology vol. 26
Availability: No items available.
|
|
|
1697.
|
Activating Mutations of the G-protein Subunit α 11 Interdomain Interface Cause Autosomal Dominant Hypocalcemia Type 2. [electronic resource] by
- Gorvin, Caroline M
- Stokes, Victoria J
- Boon, Hannah
- Cranston, Treena
- Glück, Anna K
- Bahl, Shailini
- Homfray, Tessa
- Aung, Theingi
- Shine, Brian
- Lines, Kate E
- Hannan, Fadil M
- Thakker, Rajesh V
Producer: 20201105
In:
The Journal of clinical endocrinology and metabolism vol. 105
Availability: No items available.
|
|
|
1698.
|
|
|
|
1699.
|
|
|
|
1700.
|
|