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The Library's Role in Marketing Digital Information Services during COVID-19: Al-Balqa Applied University: Case Study.
- Published in:
- International Journal of Information Science & Management, 2024, v. 22, n. 3, p. 139, doi. 10.22034/ijism.2024.1977923.0
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- Publication type:
- Article
Unraveling the genetic landscape of autosomal recessive Charcot-Marie-Tooth neuropathies using a homozygosity mapping approach.
- Published in:
- Neurogenetics, 2015, v. 16, n. 1, p. 33, doi. 10.1007/s10048-014-0422-0
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- Publication type:
- Article
Definition of the phenotypic spectrum of Temtamy preaxial brachydactyly syndrome associated with autosomal recessive CHYS1 mutations.
- Published in:
- Middle East Journal of Medical Genetics, 2012, v. 1, n. 2, p. 64, doi. 10.1097/01.MXE.0000414918.78299.94
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- Publication type:
- Article
Arthrogrypotic Syndrome is the Usual Misnomer in Children with Du Pan Syndrome.
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- American Journal of Biomedical Sciences, 2020, v. 12, n. 2, p. 91, doi. 10.5099/aj200200091
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- Publication type:
- Article
Foreign exchange rate exposure: Evidence from Canada.
- Published in:
- Review of Financial Economics, 2014, v. 23, n. 1, p. 18, doi. 10.1016/j.rfe.2013.12.001
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- Publication type:
- Article
Foreign exchange rate exposure: Evidence from Canada.
- Published in:
- Review of Financial Economics, 2004, v. 23, n. 1, p. 18, doi. 10.1016/j.rfe.2013.12.001
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- Publication type:
- Article
Clinical Phenotype and Bone Biopsy Characteristics in a Child with Proteus Syndrome.
- Published in:
- Calcified Tissue International, 2021, v. 109, n. 5, p. 586, doi. 10.1007/s00223-021-00862-z
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- Publication type:
- Article
A progeroid syndrome caused by a deep intronic variant in TAPT1 is revealed by RNA/SI‐NET sequencing.
- Published in:
- EMBO Molecular Medicine, 2023, v. 15, n. 2, p. 1, doi. 10.15252/emmm.202216478
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- Publication type:
- Article
The Impact of Sentiment on Commodity Return and Volatility.
- Published in:
- Review of Pacific Basin Financial Markets & Policies, 2020, v. 23, n. 4, p. N.PAG, doi. 10.1142/S0219091520500344
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- Publication type:
- Article
The Effects of the Use of Corporate Derivatives on the Foreign Exchange Rate Exposure.
- Published in:
- Journal of Accounting, Business & Management, 2009, v. 16, n. 1, p. 72
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- Publication type:
- Article
Haploinsufficiency for AAGAB causes clinically heterogeneous forms of punctate palmoplantar keratoderma.
- Published in:
- Nature Genetics, 2012, v. 44, n. 11, p. 1272, doi. 10.1038/ng.2444
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- Publication type:
- Article
Mutations in IRX5 impair craniofacial development and germ cell migration via SDF1.
- Published in:
- Nature Genetics, 2012, v. 44, n. 6, p. 709, doi. 10.1038/ng.2259
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- Publication type:
- Article
Mutations in PYCR1 cause cutis laxa with progeroid features.
- Published in:
- Nature Genetics, 2009, v. 41, n. 9, p. 1016, doi. 10.1038/ng.413
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- Publication type:
- Article
Arthrogryposis is a descriptive term, not a specific disease entity: Escobar Syndrome is an example.
- Published in:
- Minerva Pediatrics, 2024, v. 76, n. 1, p. 30, doi. 10.23736/S2724-5276.20.05796-5
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- Publication type:
- Article
A novel AUTS2 Variant in a Patient with Global Developmental Delay and Intellectual Disability.
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- Jordan Journal of Biological Sciences, 2024, v. 17, n. 2, p. 217, doi. 10.54319/jjbs/170201
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- Publication type:
- Article
Air Pollution and Economic Growth in MENA Countries: Testing EKC Hypothesis.
- Published in:
- Environmental Research, Engineering & Management / Aplinkos Tyrimai, Inžinerija ir Vadyba, 2014, v. 70, n. 4, p. 54, doi. 10.5755/j01.erem.70.4.7743
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- Publication type:
- Article
Recessive mutation in GALNT3 causes hyperphosphatemic familial tumoral calcinosis associated with chronic recurrent multifocal osteomyelitis.
- Published in:
- Turkish Journal of Pediatrics, 2019, v. 61, n. 1, p. 130, doi. 10.24953/turkjped.2019.01.022
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- Publication type:
- Article
Craniofacial Malformations as Fundamental Diagnostic Tools in Syndromic Entities.
- Published in:
- Diagnostics (2075-4418), 2022, v. 12, n. 10, p. 2375, doi. 10.3390/diagnostics12102375
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- Publication type:
- Article
Torticollis in Connection with Spine Phenotype.
- Published in:
- Diagnostics (2075-4418), 2022, v. 12, n. 7, p. N.PAG, doi. 10.3390/diagnostics12071672
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- Publication type:
- Article
Impact of Mitochondrial Genetic Variants in ND1, ND2, ND5, and ND6 Genes on Sperm Motility and Intracytoplasmic Sperm Injection (ICSI) Outcomes.
- Published in:
- Reproductive Sciences, 2021, v. 28, n. 5, p. 1540, doi. 10.1007/s43032-020-00449-3
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- Publication type:
- Article
C5orf42 is the major gene responsible for OFD syndrome type VI.
- Published in:
- Human Genetics, 2014, v. 133, n. 3, p. 367, doi. 10.1007/s00439-013-1385-1
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- Publication type:
- Article
Tomographic Study of the Malformation Complex in Correlation With the Genotype in Patients With Robinow Syndrome: Review Article.
- Published in:
- Journal of Investigative Medicine High Impact Case Reports, 2020, v. 8, p. 1, doi. 10.1177/2324709620911771
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- Publication type:
- Article
Tomographic Study of the Malformation Complex in Correlation With the Genotype in Patients With Robinow Syndrome: Review Article.
- Published in:
- Journal of Investigative Medicine High Impact Case Reports, 2020, v. 8, n. 1, p. 1, doi. 10.1177/2324709620911771
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- Publication type:
- Article
Have the extraordinary circumstances of the COVID-19 outbreak and the Russian–Ukrainian conflict impacted the efficiency of cryptocurrencies?
- Published in:
- Financial Innovation, 2024, v. 10, n. 1, p. 1, doi. 10.1186/s40854-023-00550-x
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- Publication type:
- Article
INTS13 variants causing a recessive developmental ciliopathy disrupt assembly of the Integrator complex.
- Published in:
- Nature Communications, 2022, v. 13, n. 1, p. 1, doi. 10.1038/s41467-022-33547-8
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- Publication type:
- Article
Infantile systemic hyalinosis: Variable grades of severity.
- Published in:
- 2021
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- Publication type:
- journal article
Deficiency of lrp4 in zebrafish and human LRP4 mutation induce aberrant activation of Jagged-Notch signaling in fin and limb development.
- Published in:
- Cellular & Molecular Life Sciences, 2019, v. 76, n. 1, p. 163, doi. 10.1007/s00018-018-2928-3
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- Publication type:
- Article
Did real economic uncertainty drive risk connectedness in the oil–stock nexus during the COVID-19 outbreak? A partial wavelet coherence analysis.
- Published in:
- Journal of Economic Structures, 2023, v. 12, n. 1, p. 1, doi. 10.1186/s40008-023-00306-x
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- Publication type:
- Article
Long memory behavior in Singapore's tourism market.
- Published in:
- International Journal of Tourism Research, 2017, v. 19, n. 5, p. 524, doi. 10.1002/jtr.2125
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- Publication type:
- Article
Bioenergetic analysis of aged‐phenotype skin in a rare syndromic cutis laxa.
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- Journal of Cosmetic Dermatology, 2021, v. 20, n. 9, p. 2999, doi. 10.1111/jocd.13951
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- Publication type:
- Article
Case report: Dihydropyridine receptor (CACNA1S) congenital myopathy, a novel phenotype with early onset periodic paralysis.
- Published in:
- Frontiers in Neurology, 2024, p. 1, doi. 10.3389/fneur.2024.1359479
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- Publication type:
- Article
Prevalence of coagulation factor II G20210A and factor V G1691A Leiden polymorphisms in Chechans, a genetically isolated population in Jordan.
- Published in:
- Molecular Biology Reports, 2012, v. 39, n. 9, p. 9133, doi. 10.1007/s11033-012-1785-7
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- Publication type:
- Article
Loss of the scavenger mRNA decapping enzyme DCPS causes syndromic intellectual disability with neuromuscular defects.
- Published in:
- Human Molecular Genetics, 2015, v. 24, n. 11, p. 3163, doi. 10.1093/hmg/ddv067
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- Publication type:
- Article
ThalassoChip, an array mutation and single nucleotide polymorphism detection tool for the diagnosis of β-thalassaemia.
- Published in:
- Clinical Chemistry & Laboratory Medicine, 2010, v. 48, n. 12, p. 1713, doi. 10.1515/CCLM.2010.331
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- Publication type:
- Article
Skeletal phenotype/genotype in progressive pseudorheumatoid chondrodysplasia.
- Published in:
- Clinical Rheumatology, 2020, v. 39, n. 2, p. 553, doi. 10.1007/s10067-019-04783-z
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- Publication type:
- Article
Association between vitamin D metabolism gene polymorphisms and schizophrenia.
- Published in:
- Biomedical Reports, 2024, v. 21, n. 3, p. N.PAG, doi. 10.3892/br.2024.1822
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- Publication type:
- Article