Found: 21
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Outcome of array CGH analysis for 255 subjects with intellectual disability and search for candidate genes using bioinformatics.
- Published in:
- Human Genetics, 2010, v. 128, n. 2, p. 179, doi. 10.1007/s00439-010-0837-0
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- Publication type:
- Article
DNA damage to spermatozoa has impacts on fertilization and pregnancy.
- Published in:
- Cell & Tissue Research, 2005, v. 322, n. 1, p. 33, doi. 10.1007/s00441-005-1097-5
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- Publication type:
- Article
Prenatally detected trisomy 20 mosaicism.
- Published in:
- Prenatal Diagnosis, 2005, v. 25, n. 3, p. 239, doi. 10.1002/pd.1121
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- Publication type:
- Article
Increased concentrations of the oxidative DNA adduct 7,8-dihydro-8-oxo-2-deoxyguanosine in the germ-line of men with type 1 diabetes.
- Published in:
- Reproductive BioMedicine Online (Reproductive Healthcare Limited), 2008, v. 16, n. 3, p. 401, doi. 10.1016/S1472-6483(10)60602-5
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- Publication type:
- Article
Identification of protein changes in human spermatozoa throughout the cryopreservation process.
- Published in:
- Andrology, 2017, v. 5, n. 1, p. 10, doi. 10.1111/andr.12279
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- Publication type:
- Article
Face–brain asymmetry in autism spectrum disorders.
- Published in:
- Molecular Psychiatry, 2008, v. 13, n. 6, p. 614, doi. 10.1038/mp.2008.18
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- Publication type:
- Article
Mitochondrial DNA deletions and nuclear DNA fragmentation in testicular and epididymal human sperm.
- Published in:
- 2002
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- Publication type:
- journal article
A comparison of mitochondrial and nuclear DNA status in testicular sperm from fertile men and those with obstructive azoospermia.
- Published in:
- 2002
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- Publication type:
- journal article
The effects of cryopreservation on sperm morphology, motility and mitochondrial function.
- Published in:
- 2002
- By:
- Publication type:
- journal article
A genome-wide DNA methylation signature for SETD1B-related syndrome.
- Published in:
- Clinical Epigenetics, 2019, v. 11, n. 1, p. N.PAG, doi. 10.1186/s13148-019-0749-3
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- Publication type:
- Article
The effects of pentoxifylline on the generation of reactive oxygen species and lipid peroxidation in human spermatozoa.
- Published in:
- Andrologia, 1996, v. 28, n. 1, p. 15, doi. 10.1111/j.1439-0272.1996.tb02752.x
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- Publication type:
- Article
Autism severity is associated with child and maternal MAOA genotypes.
- Published in:
- Clinical Genetics, 2011, v. 79, n. 4, p. 355, doi. 10.1111/j.1399-0004.2010.01471.x
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- Publication type:
- Article
Autism-associated familial microdeletion of Xp11.22.
- Published in:
- Clinical Genetics, 2008, v. 74, n. 2, p. 134, doi. 10.1111/j.1399-0004.2008.01028.x
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- Publication type:
- Article
15q Duplication associated with autism in a multiplex family with a familial cryptic translocation t(14;15)(q11.2;q13.3) detected using array-CGH.
- Published in:
- Clinical Genetics, 2006, v. 69, n. 2, p. 124, doi. 10.1111/j.1399-0004.2005.00560.x
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- Publication type:
- Article
Loud and clear evidence for gene silencing by epigenetic mechanisms in autism spectrum and related neurodevelopmental disorders.
- Published in:
- Clinical Genetics, 2006, v. 69, n. 1, p. 21, doi. 10.1111/j.1399-0004.2006.00543a.x
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- Publication type:
- Article
Putting mind over matter: rethinking current strategies for unmasking the genetics of mental illness.
- Published in:
- 2004
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- Publication type:
- Other
The complicity of segmental duplicity in human genetic disease.
- Published in:
- Clinical Genetics, 2003, v. 63, n. 4, p. 262, doi. 10.1034/j.1399-0004.2003.00068.x
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- Publication type:
- Article
Nature's accounting: the gains, losses and human cost of duplicon-mediated genomic imbalance.
- Published in:
- Clinical Genetics, 2003, v. 63, n. 4, p. 262, doi. 10.1034/j.1399-0004.2003.t01-1-00068.x
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- Publication type:
- Article
Chromosome 22: a little chromosome that presents a larger understanding of genomic disorders.
- Published in:
- Clinical Genetics, 2003, v. 63, n. 4, p. 264, doi. 10.1034/j.1399-0004.2003.t01-2-00068.x
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- Publication type:
- Article
Searching the vast array of genomic disorders.
- Published in:
- Clinical Genetics, 2003, v. 63, n. 4, p. 266, doi. 10.1034/j.1399-0004.2003.t01-3-00068.x
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- Publication type:
- Article
Putatively benign copy number variants in subjects with idiopathic autism spectrum disorder and/or intellectual disability.
- Published in:
- Cytogenetic & Genome Research, 2009, v. 123, n. 1-4, p. 79, doi. 10.1159/000184694
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- Publication type:
- Article