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Demonstration of uniparental-isodisomy on chromosome 22q11.2 in a patient with childhood schizophrenia and facial dysmorphology by whole-genome analysis. [electronic resource] by
- Cogulu, Ozgur
- Pariltay, Erhan
- Durmaz, Asude Alpman
- Aykut, Ayca
- Gunduz, Cumhur
- Ozbaran, Burcu
- Aydin, Hikmet Hakan
- Erermis, Serpil
- Aydin, Cahide
- Ozkinay, Ferda
Producer: 20120808
In:
The Journal of neuropsychiatry and clinical neurosciences vol. 24
Availability: No items available.
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Genome-wide paternal uniparental disomy as a cause of Beckwith-Wiedemann syndrome associated with recurrent virilizing adrenocortical tumors. [electronic resource] by
- Bertoin, F
- Letouzé, E
- Grignani, P
- Patey, M
- Rossignol, S
- Libé, R
- Pasqual, C
- Lardière-Deguelte, S
- Hoeffel-Fornes, C
- Gaillard, D
- Previderè, C
- Delemer, B
- Lalli, E
Producer: 20160229
In:
Hormone and metabolic research = Hormon- und Stoffwechselforschung = Hormones et metabolisme vol. 47
Availability: No items available.
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