Found: 4
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Partial deficiency of 17γ-hydroxylase/17,20-lyase caused by a novel missense mutation in the canonical cytochrome heme-interacting motif.
- Published in:
- European Journal of Endocrinology, 2015, v. 172, n. 5, p. K19, doi. 10.1530/EJE-14-0834
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- Article
A Novel Mutation in the Critical P-Box Residue of Steroidogenic Factor-1 Presenting with XY Sex Reversal and Transient Adrenal Failure.
- Published in:
- Hormone Research in Paediatrics, 2018, v. 89, n. 6, p. 450, doi. 10.1159/000481776
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- Article
High-throughput mutagenesis identifies mutations and RNA-binding proteins controlling CD19 splicing and CART-19 therapy resistance.
- Published in:
- Nature Communications, 2022, v. 13, n. 1, p. 1, doi. 10.1038/s41467-022-31818-y
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- Article
Synovial lipomatosis of the stifle joint in a dog.
- Published in:
- Veterinary Record Case Reports, 2021, v. 9, n. 4, p. 1, doi. 10.1002/vrc2.163
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- Publication type:
- Article