Results
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Intellectual disability in patients with MODY due to hepatocyte nuclear factor 1B (HNF1B) molecular defects. [electronic resource] by
- Dubois-Laforgue, D
- Bellanné-Chantelot, C
- Charles, P
- Jacquette, A
- Larger, E
- Ciangura, C
- Saint-Martin, C
- Rastel, C
- Keren, B
- Timsit, J
Producer: 20170323
In:
Diabetes & metabolism vol. 43
Availability: No items available.
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Identification of novel HNF1B mRNA splicing variants and their qualitative and semi-quantitative profile in selected healthy and tumour tissues. [electronic resource] by
- Hojny, Jan
- Bartu, Michaela
- Krkavcova, Eva
- Nemejcova, Kristyna
- Sevcik, Jan
- Cibula, David
- Fryba, Vladimir
- Plincelnerova, Lenka
- Dundr, Pavel
- Struzinska, Ivana
Producer: 20201214
In:
Scientific reports vol. 10
Availability: No items available.
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Mutations in the hepatocyte nuclear factor-1β (HNF1B) gene are common with combined uterine and renal malformations but are not found with isolated uterine malformations. [electronic resource] by
- Oram, Richard A
- Edghill, Emma L
- Blackman, Jenny
- Taylor, Miles J O
- Kay, Tracey
- Flanagan, Sarah E
- Ismail-Pratt, Ida
- Creighton, Sarah M
- Ellard, Sian
- Hattersley, Andrew T
- Bingham, Coralie
Producer: 20101101
In:
American journal of obstetrics and gynecology vol. 203
Availability: No items available.
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