Found: 7
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O09 Targeted genetic therapy for congenital melanocytic naevi.
- Published in:
- British Journal of Dermatology, 2024, v. 190, p. i4, doi. 10.1093/bjd/ljad483.009
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- Publication type:
- Article
Tissue- and ethnicity-independent hypervariable DNA methylation states show evidence of establishment in the early human embryo.
- Published in:
- Nucleic Acids Research, 2022, v. 50, n. 12, p. 6735, doi. 10.1093/nar/gkac503
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- Publication type:
- Article
Diverse species-specific phenotypic consequences of loss of function sorting nexin 14 mutations.
- Published in:
- Scientific Reports, 2020, v. 10, n. 1, p. 1, doi. 10.1038/s41598-020-70797-2
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- Publication type:
- Article
Exome sequencing identifies variants in FKBP4 that are associated with recurrent fetal loss in humans.
- Published in:
- Human Molecular Genetics, 2019, v. 28, n. 20, p. 3466, doi. 10.1093/hmg/ddz203
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- Publication type:
- Article
SNX14 mutations affect endoplasmic reticulum-associated neutral lipid metabolism in autosomal recessive spinocerebellar ataxia 20.
- Published in:
- Human Molecular Genetics, 2018, v. 27, n. 11, p. 1927, doi. 10.1093/hmg/ddy101
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- Publication type:
- Article
Genetic Analyses in Small-for-Gestational-Age Newborns.
- Published in:
- 2018
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- Publication type:
- journal article
Paternally Expressed, Imprinted Insulin-Like Growth Factor-2 in Chorionic Villi Correlates Significantly with Birth Weight.
- Published in:
- PLoS ONE, 2014, v. 9, n. 1, p. 1, doi. 10.1371/journal.pone.0085454
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- Publication type:
- Article