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Comprehensive molecular analysis identifies eight novel variants in XY females with disorders of sex development.
- Published in:
- Molecular Human Reproduction, 2023, v. 29, n. 2, p. 1, doi. 10.1093/molehr/gaad001
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- Publication type:
- Article
Correction to: Novel deletion of exon 3 in TYR gene causing Oculocutaneous albinism 1B in an Indian family along with intellectual disability associated with chromosomal copy number variations.
- Published in:
- 2022
- By:
- Publication type:
- Correction Notice
Novel deletion of exon 3 in TYR gene causing Oculocutaneous albinism 1B in an Indian family along with intellectual disability associated with chromosomal copy number variations.
- Published in:
- BMC Medical Genomics, 2022, v. 15, n. 1, p. 1, doi. 10.1186/s12920-021-01152-1
- By:
- Publication type:
- Article
Novel deletion of exon 3 in TYR gene causing Oculocutaneous albinism 1B in an Indian family along with intellectual disability associated with chromosomal copy number variations.
- Published in:
- BMC Medical Genomics, 2022, v. 15, n. 1, p. 1, doi. 10.1186/s12920-021-01152-1
- By:
- Publication type:
- Article