Found: 7
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Extremely skewed X-chromosome inactivation is increased in pre-eclampsia.
- Published in:
- Human Genetics, 2007, v. 121, n. 1, p. 101, doi. 10.1007/s00439-006-0281-3
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- Article
ALX4 dysfunction disrupts craniofacial and epidermal development.
- Published in:
- Human Molecular Genetics, 2009, v. 18, n. 22, p. 4357, doi. 10.1093/hmg/ddp391
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- Article
Evidence from autoimmune thyroiditis of skewed X-chromosome inactivation in female predisposition to autoimmunity.
- Published in:
- European Journal of Human Genetics, 2006, v. 14, n. 6, p. 791, doi. 10.1038/sj.ejhg.5201614
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- Article
Mutations in IRX5 impair craniofacial development and germ cell migration via SDF1.
- Published in:
- Nature Genetics, 2012, v. 44, n. 6, p. 709, doi. 10.1038/ng.2259
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- Article
KIF7 mutations cause fetal hydrolethalus and acrocallosal syndromes.
- Published in:
- Nature Genetics, 2011, v. 43, n. 6, p. 601, doi. 10.1038/ng.826
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- Article
Extreme Clonality in Lymphoblastoid Cell Lines with Implications for Allele Specific Expression Analyses.
- Published in:
- PLoS ONE, 2008, v. 3, n. 8, p. 1, doi. 10.1371/journal.pone.0002966
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- Article
TMCO1 deficiency causes autosomal recessive cerebrofaciothoracic dysplasia.
- Published in:
- American Journal of Medical Genetics. Part A, 2014, v. 164A, n. 2, p. 291, doi. 10.1002/ajmg.a.36248
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- Article