Found: 6
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Imprinted expression of UBE3A in non-neuronal cells from a Prader–Willi syndrome patient with an atypical deletion.
- Published in:
- Human Molecular Genetics, 2014, v. 23, n. 9, p. 2364, doi. 10.1093/hmg/ddt628
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- Publication type:
- Article
A deletion of the HBII-85 class of small nucleolar RNAs (snoRNAs) is associated with hyperphagia, obesity and hypogonadism.
- Published in:
- Human Molecular Genetics, 2009, v. 18, n. 17, p. 3257, doi. 10.1093/hmg/ddp263
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- Publication type:
- Article
Array CGH analysis of copy number variation identifies 1284 new genes variant in healthy white males: implications for association studies of complex diseases.
- Published in:
- Human Molecular Genetics, 2007, v. 16, n. 23, p. 2783, doi. 10.1093/hmg/ddm208
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- Article
Genetics of obesity and the prediction of risk for health.
- Published in:
- Human Molecular Genetics, 2006, v. 15, n. 2, p. r124, doi. 10.1093/hmg/ddl215
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- Publication type:
- Article
Genetics of obesity and the prediction of risk for health.
- Published in:
- Human Molecular Genetics, 2006, v. 15, n. suppl_2, p. R124, doi. 10.1093/hmg/ddl215
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- Publication type:
- Article
Chromosome 19p13.3 deletion in a patient with macrocephaly, obesity, mental retardation, and behavior problems.
- Published in:
- American Journal of Medical Genetics. Part A, 2011, v. 155A, n. 5, p. 1192, doi. 10.1002/ajmg.a.33986
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- Publication type:
- Article