Found: 8
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Hypospadias associated with hypertelorism, the mildest phenotype of Opitz syndrome.
- Published in:
- Journal of Human Genetics, 2011, v. 56, n. 5, p. 348, doi. 10.1038/jhg.2011.17
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- Article
Corrigendum: Common variants in DGKK are strongly associated with risk of hypospadias.
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- 2011
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- Correction Notice
Common variants in DGKK are strongly associated with risk of hypospadias.
- Published in:
- Nature Genetics, 2011, v. 43, n. 1, p. 48, doi. 10.1038/ng.721
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- Article
Fine mapping analysis confirms and strengthens linkage of four chromosomal regions in familial hypospadias.
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- European Journal of Human Genetics, 2015, v. 23, n. 4, p. 516, doi. 10.1038/ejhg.2014.129
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- Article
Genome-wide identification of quantitative trait loci in a cross between Hampshire and Landrace II: Meat quality traits.
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- BMC Genetics, 2008, v. 9, p. 1, doi. 10.1186/1471-2156-9-22
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- Article
Further support linking the 22q11.2 microduplication to an increased risk of bladder exstrophy and highlighting LZTR1 as a candidate gene.
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- Molecular Genetics & Genomic Medicine, 2019, v. 7, n. 6, p. N.PAG, doi. 10.1002/mgg3.666
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- Article
WNT3 involvement in human bladder exstrophy and cloaca development in zebrafish.
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- Human Molecular Genetics, 2015, v. 24, n. 18, p. 5069, doi. 10.1093/hmg/ddv225
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- Article
ZBED6, a Novel Transcription Factor Derived from a Domesticated DNA Transposon Regulates IGF2 Expression and Muscle Growth.
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- PLoS Biology, 2009, v. 7, n. 12, p. 1, doi. 10.1371/journal.pbio.1000256
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- Article