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A premature termination mutation in a patient with Lowe syndrome without congenital cataracts: dropping the "O" in OCRL. [electronic resource] by
- Pasternack, S M
- Böckenhauer, D
- Refke, M
- Tasic, V
- Draaken, M
- Conrad, C
- Born, M
- Betz, R C
- Reutter, H
- Ludwig, M
Producer: 20130805
In:
Klinische Padiatrie vol. 225
Availability: No items available.
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40.
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Duplication of The [electronic resource] by
- Tasic, V
- Mitrotti, A
- Riepe, F G
- Kulle, A E
- Laban, N
- Polenakovic, M
- Plaseska-Karanfilska, D
- Sanna-Cherchi, S
- Kostovski, M
- Gucev, Z
Publication details: Balkan journal of medical genetics : BJMG Jun 2019
In:
Balkan journal of medical genetics : BJMG vol. 22
Availability: No items available.
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