Found: 13
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Targeted SLC19A3 gene sequencing of 3000 Saudi newborn: a pilot study toward newborn screening.
- Published in:
- Annals of Clinical & Translational Neurology, 2019, v. 6, n. 10, p. 2097, doi. 10.1002/acn3.50898
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- Publication type:
- Article
Feasibility of Responsive Teaching With Mothers and Young Children With Autism in Saudi Arabia.
- Published in:
- Journal of Early Intervention, 2018, v. 40, n. 4, p. 304, doi. 10.1177/1053815118789176
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- Publication type:
- Article
Molecular Analysis of Congenital Hypothyroidism in Saudi Arabia: SLC26A7 Mutation Is a Novel Defect in Thyroid Dyshormonogenesis.
- Published in:
- 2018
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- Publication type:
- journal article
Assessment of the Knowledge and Attitudes of Saudi Mothers towards Newborn Screening.
- Published in:
- BioMed Research International, 2015, v. 2015, p. 1, doi. 10.1155/2015/718674
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- Publication type:
- Article
A novel X-linked disorder with developmental delay and autistic features.
- Published in:
- Annals of Neurology, 2012, v. 71, n. 4, p. 498, doi. 10.1002/ana.22673
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- Publication type:
- Article
Arginine 16 Glycine Polymorphism in β2-Adrenergic Receptor Gene Is Associated with Obesity, Hyperlipidemia, Hyperleptinemia, and Insulin Resistance in Saudis.
- Published in:
- International Journal of Endocrinology, 2012, p. 1, doi. 10.1155/2012/945608
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- Publication type:
- Article
Erratum: Preimplantation genetic diagnosis in Saudi Arabia: parents' experience and attitudes.
- Published in:
- Prenatal Diagnosis, 2011, v. 31, n. 4, p. 415, doi. 10.1002/pd.2649
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- Publication type:
- Article
Chromosome 12q24.31-q24.33 deletion causes multiple dysmorphic features and developmental delay: First mosaic patient and overview of the phenotype related to 12q24qter defects.
- Published in:
- Molecular Cytogenetics (17558166), 2011, v. 4, n. 1, p. 9, doi. 10.1186/1755-8166-4-9
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- Publication type:
- Article
Medium‐chain acyl‐CoA dehydrogenase deficiency in Saudi Arabia: incidence, genotype, and preventive implications.
- Published in:
- Journal of Inherited Metabolic Disease, 2010, v. 33, p. 263, doi. 10.1007/s10545-010-9143-1
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- Publication type:
- Article
Preimplantation genetic diagnosis in Saudi Arabia: parents' experience and attitudes.
- Published in:
- Prenatal Diagnosis, 2010, v. 30, n. 8, p. 753, doi. 10.1002/pd.2532
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- Publication type:
- Article
The Gln27Glu Polymorphism in β2-Adrenergicreceptor gene is linked to hypertriglyceridemia,hyperinsulinemia and hyperleptinemia in Saudis.
- Published in:
- Lipids in Health & Disease, 2010, v. 9, p. 90, doi. 10.1186/1476-511X-9-90
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- Publication type:
- Article
Preimplantation genetic diagnosis for Niemann-Pick disease type B.
- Published in:
- Prenatal Diagnosis, 2004, v. 24, n. 12, p. 943, doi. 10.1002/pd.1050
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- Publication type:
- Article
Multiple displacement amplification on single cell and possible PGD applications.
- Published in:
- Molecular Human Reproduction, 2004, v. 10, n. 11, p. 847, doi. 10.1093/molehr/gah114
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- Publication type:
- Article