Found: 26
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Genetics of multifactorial disorders: proceedings of the 6th Pan Arab Human Genetics Conference.
- Published in:
- 2016
- By:
- Publication type:
- journal article
A Novel Variant in the Endothelin-Converting Enzyme-Like 1 (ECEL1) Gene in an Emirati Child.
- Published in:
- 2017
- By:
- Publication type:
- journal article
Marinesco-Sjögren Syndrome in an Emirati Child with a Novel Mutation in SIL1 Affecting the 5' Untranslated Region.
- Published in:
- 2016
- By:
- Publication type:
- journal article
Incidence of Down Syndrome in Dubai, UAE.
- Published in:
- Medical Principles & Practice, 2007, v. 16, n. 1, p. 25, doi. 10.1159/000096136
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- Publication type:
- Article
Clinical and Molecular Update on the Fourth Reported Family with Hamamy Syndrome.
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- Molecular Syndromology, 2021, v. 12, n. 6, p. 342, doi. 10.1159/000517253
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- Publication type:
- Article
Barriers of Adherence among Palestinian Healthcare Professionals towards the Protocol of Health Education and Counselling on Healthy Behaviours for Non-Communicable Diseases.
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- Ethiopian Journal of Health Sciences, 2021, v. 31, n. 1, p. 73, doi. 10.4314/ejhs.v31i1.9
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- Publication type:
- Article
Developmental delay, intellectual disability, short stature, subglottic stenosis, hearing impairment, onychodysplasia of the index fingers, and distinctive facial features: A newly reported autosomal recessive syndrome.
- Published in:
- American Journal of Medical Genetics. Part A, 2020, v. 182, n. 8, p. 1865, doi. 10.1002/ajmg.a.61730
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- Publication type:
- Article
Microcephalic primordial dwarfism in an Emirati patient with PNKP mutation.
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- American Journal of Medical Genetics. Part A, 2016, v. 170A, n. 8, p. 2127, doi. 10.1002/ajmg.a.37766
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- Publication type:
- Article
Identification of a novel CTCF mutation responsible for syndromic intellectual disability – a case report.
- Published in:
- 2017
- By:
- Publication type:
- Case Study
Identification of a novel homozygous UNC80 variant in a child with infantile hypotonia with psychomotor retardation and characteristic facies-2 (IHPRF2).
- Published in:
- Metabolic Brain Disease, 2018, v. 33, n. 3, p. 869, doi. 10.1007/s11011-018-0200-z
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- Publication type:
- Article
Meta-analyses of the association of HLA- DRB1 alleles with rheumatoid arthritis among Arabs.
- Published in:
- International Journal of Rheumatic Diseases, 2017, v. 20, n. 7, p. 832, doi. 10.1111/1756-185X.12922
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- Publication type:
- Article
CTGA: the database for genetic disorders in Arab populations.
- Published in:
- Nucleic Acids Research, 2006, v. 34, n. suppl 1, p. d602, doi. 10.1093/nar/gkj015
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- Publication type:
- Article
Public Sector Capacity to Prevent and Control of Noncommunicable Diseases in Twelve Low- and Middle-Income Countries Based on WHO-PEN Standards: A Systematic Review.
- Published in:
- Health Services Insights, 2021, v. 14, p. 1, doi. 10.1177/1178632920986233
- By:
- Publication type:
- Article
Public Sector Capacity to Prevent and Control of Noncommunicable Diseases in Twelve Low- and Middle-Income Countries Based on WHO-PEN Standards: A Systematic Review.
- Published in:
- Health Services Insights, 2021, v. 14, p. 1, doi. 10.1177/1178632920986233
- By:
- Publication type:
- Article
Novel PDE6A mutation in an Emirati patient with retinitis pigmentosa.
- Published in:
- 2017
- By:
- Publication type:
- Case Study
A novel, putatively null, FGD1 variant leading to Aarskog-Scott syndrome in a family from UAE.
- Published in:
- 2017
- By:
- Publication type:
- journal article
A 20-year Clinical and Genetic Neuromuscular Cohort Analysis in Lebanon: An International Effort.
- Published in:
- Journal of Neuromuscular Diseases, 2022, v. 9, n. 1, p. 193, doi. 10.3233/JND-210652
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- Publication type:
- Article
Single-center experience of N-linked Congenital Disorders of Glycosylation with a Summary of Molecularly Characterized Cases in Arabs.
- Published in:
- Annals of Human Genetics, 2018, v. 82, n. 1, p. 35, doi. 10.1111/ahg.12220
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- Publication type:
- Article
Barriers toward the practice of healthy behaviors among patients with non-communicable diseases in Gaza Strip, Palestine.
- Published in:
- SAGE Open Medicine, 2021, v. 9, p. 1, doi. 10.1177/20503121211029179
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- Publication type:
- Article
Effects of Ramadan fasting on anthropometric measures, blood pressure, and lipid profile among hypertensive patients in the Kurdistan region of Iraq.
- Published in:
- SAGE Open Medicine, 2020, p. 1, doi. 10.1177/2050312120965780
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- Publication type:
- Article
Effects of Ramadan fasting on anthropometric measures, blood pressure, and lipid profile among hypertensive patients in the Kurdistan region of Iraq.
- Published in:
- SAGE Open Medicine, 2020, v. 8, p. 1, doi. 10.1177/2050312120965780
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- Publication type:
- Article
Assessment of the role of cone beam computed sialography in diagnosing salivary gland lesions.
- Published in:
- Imaging Science in Dentistry, 2013, v. 43, n. 1, p. 17, doi. 10.5624/isd.2013.43.1.17
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- Publication type:
- Article
Identification of a Novel Homozygous INSR Variant in a Patient with Rabson-Mendenhall Syndrome from the United Arab Emirates.
- Published in:
- Hormone Research in Paediatrics, 2017, v. 87, n. 1, p. 64, doi. 10.1159/000447090
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- Publication type:
- Article
Genomics into Healthcare: The 5th Pan Arab Human Genetics Conference and 2013 Golden Helix Symposium.
- Published in:
- Human Mutation, 2014, v. 35, n. 5, p. 637, doi. 10.1002/humu.22530
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- Publication type:
- Article
Spectrum of genetic disorders and gene variants in the United Arab Emirates national population: insights from the CTGA database.
- Published in:
- Frontiers in Genetics, 2023, p. 1, doi. 10.3389/fgene.2023.1177204
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- Publication type:
- Article
Catalogue for Transmission Genetics in Arabs (CTGA) Database: Analysing Lebanese Data on Genetic Disorders.
- Published in:
- Genes, 2021, v. 12, n. 10, p. 1518, doi. 10.3390/genes12101518
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- Publication type:
- Article