Found: 15
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Polymorphism at VNTR Locus 3′ to the apolipoprotein B gene in a tunisian population: Difference from other ethnic groups.
- Published in:
- Genetic Epidemiology, 1995, v. 12, n. 4, p. 381, doi. 10.1002/gepi.1370120406
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- Publication type:
- Article
Estimating the Total Pathogenic Allele Frequency of Autosomal Recessive Disorders in Case of Consanguinity.
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- Human Heredity, 2016, v. 80, n. 2, p. 69, doi. 10.1159/000438862
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- Publication type:
- Article
CONSANGUINITY AND HOMOZYGOSITY AMONG TUNISIAN PATIENTS WITH AN AUTOSOMAL RECESSIVE DISORDER.
- Published in:
- 2015
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- Publication type:
- journal article
The first missense mutation of NHS gene in a Tunisian family with clinical features of NHS syndrome including cardiac anomaly.
- Published in:
- European Journal of Human Genetics, 2011, v. 19, n. 8, p. 851, doi. 10.1038/ejhg.2011.52
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- Publication type:
- Article
A novel splice mutation in PAK3 gene underlying mental retardation with neuropsychiatric features.
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- European Journal of Human Genetics, 2008, v. 16, n. 11, p. 1358, doi. 10.1038/ejhg.2008.103
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- Publication type:
- Article
Family history predictors of BRCA1/BRCA2 mutation status among Tunisian breast/ovarian cancer families.
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- Breast Cancer (13406868), 2017, v. 24, n. 2, p. 238, doi. 10.1007/s12282-016-0693-4
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- Publication type:
- Article
High-resolution melting (HRM) assay for the detection of recurrent BRCA1/BRCA2 germline mutations in Tunisian breast/ovarian cancer families.
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- Familial Cancer, 2014, v. 13, n. 4, p. 603, doi. 10.1007/s10689-014-9740-5
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- Article
Allele Frequency Distribution of the D1S80 VNTR Locus in a Tunisian Population.
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- Journal of Forensic Sciences, 2005, v. 50, n. 5, p. 1237, doi. 10.1520/JFS2005185
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- Publication type:
- Article
Subtelomeric Microduplications in Three Sisters with Moderate Mental Retardation.
- Published in:
- Biochemical Genetics, 2010, v. 48, n. 11/12, p. 909, doi. 10.1007/s10528-010-9371-y
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- Publication type:
- Article
MLPA Subtelomere Analysis in Tunisian Mentally Retarded Patients.
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- Biochemical Genetics, 2009, v. 47, n. 9/10, p. 727, doi. 10.1007/s10528-009-9271-1
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- Publication type:
- Article
The Creatine Transporter Gene Paralogous at 16p11.2 Is Expressed in Human Brain.
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- Comparative & Functional Genomics, 2008, p. 1, doi. 10.1155/2008/609684
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- Publication type:
- Article
Exploring the 7p22.1 Chromosome as a Candidate Region for Autism.
- Published in:
- Journal of Biomedicine & Biotechnology, 2010, p. 1, doi. 10.1155/2010/423894
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- Publication type:
- Article
Absence of mutations in four genes encoding for congenital cataract and expressed in the human brain in Tunisian families with cataract and mental retardation.
- Published in:
- 2011
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- Publication type:
- journal article
Genetics and genomic medicine in Tunisia.
- Published in:
- Molecular Genetics & Genomic Medicine, 2018, v. 6, n. 2, p. 134, doi. 10.1002/mgg3.392
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- Publication type:
- Article
ARX, a novel Prd-class-homeobox gene highly expressed in the telencephalon, is mutated in X-linked mental retardation.
- Published in:
- Human Molecular Genetics, 2002, v. 11, n. 8, p. 981, doi. 10.1093/hmg/11.8.981
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- Publication type:
- Article