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Identification of Gene Signature as Diagnostic and Prognostic Blood Biomarker for Early Hepatocellular Carcinoma Using Integrated Cross-Species Transcriptomic and Network Analyses.
- Published in:
- Frontiers in Genetics, 2021, v. 12, p. 1, doi. 10.3389/fgene.2021.710049
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- Article
Chromosome 9p terminal deletion in nine Egyptian patients and narrowing of the critical region for trigonocephaly.
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- Molecular Genetics & Genomic Medicine, 2021, v. 9, n. 11, p. 1, doi. 10.1002/mgg3.1829
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- Article
Microcephalic osteodysplastic primordial dwarfism type II: Additional nine patients with implications on phenotype and genotype correlation.
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- American Journal of Medical Genetics. Part A, 2020, v. 182, n. 6, p. 1407, doi. 10.1002/ajmg.a.61585
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- Article
Biallelic novel missense HHAT variant causes syndromic microcephaly and cerebellar‐vermis hypoplasia.
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- American Journal of Medical Genetics. Part A, 2019, v. 179, n. 6, p. 1053, doi. 10.1002/ajmg.a.61133
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- Article
Identification of a novel homozygous <italic>ALX4</italic> mutation in two unrelated patients with frontonasal dysplasia type‐2.
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- American Journal of Medical Genetics. Part A, 2018, v. 176, n. 5, p. 1190, doi. 10.1002/ajmg.a.38655
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- Article
Clinical features of SMARCA2 duplication overlap with Coffin-Siris syndrome.
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- American Journal of Medical Genetics. Part A, 2016, v. 170A, n. 10, p. 2662, doi. 10.1002/ajmg.a.37778
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- Article
De Novo 17q24.2-q24.3 microdeletion presenting with generalized hypertrichosis terminalis, gingival fibromatous hyperplasia, and distinctive facial features.
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- American Journal of Medical Genetics. Part A, 2015, v. 167A, n. 10, p. 2418, doi. 10.1002/ajmg.a.37185
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- Article
A homozygous mutation in RNU4ATAC as a cause of microcephalic osteodysplastic primordial dwarfism type I (MOPD I) with associated pigmentary disorder.
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- American Journal of Medical Genetics. Part A, 2011, v. 155A, n. 11, p. 2885, doi. 10.1002/ajmg.a.34299
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- Publication type:
- Article
Exploring Telomere Length in Progeroid Syndromes Through Quantitative Fluorescence In-Situ Hybridization (QFISH).
- Published in:
- Middle East Journal of Medical Genetics, 2023, v. 12, n. 1, p. 1, doi. 10.21608/MXE.2024.254410.1009
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- Article
Trials for Implementing Cost-effective Fanconi Anemia (FA) Molecular Diagnosis.
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- Middle East Journal of Medical Genetics, 2022, v. 11, n. 2, p. 58, doi. 10.21608/MXE.2023.287527
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- Publication type:
- Article
Fanconi and Non-Fanconi anemia: A Single Center Experience of A Large Egyptian Cohort.
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- Middle East Journal of Medical Genetics, 2022, v. 11, n. 1, p. 19, doi. 10.21608/MXE.2023.283879
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- Article
Clinical implementation of sperm DNA fragmentation studies in the assessment of male unexplained infertility.
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- Middle East Journal of Medical Genetics, 2021, v. 10, n. 1, p. 1
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- Article
Clinical and cytogenetic description of three patients with constitutional mosaic trisomy 8.
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- Middle East Journal of Medical Genetics, 2017, v. 8, n. 1, p. 29, doi. 10.1097/01.MXE.0000511080.21083.0a
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- Article
Cytogenetics abnormalities in a referred population for chromosomal analysis and the role of fluorescence in-situ hybridization in refining the diagnosis.
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- Middle East Journal of Medical Genetics, 2017, v. 8, n. 1, p. 13, doi. 10.1097/01.MXE.0000510783.68308.a4
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- Article
Evaluation of the frequency of sister chromatid exchanges and micronuclei in children with type-1 diabetes mellitus.
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- Middle East Journal of Medical Genetics, 2016, v. 5, n. 1, p. 26, doi. 10.1097/01.MXE.0000475220.51742.95
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- Article
Cytogenetics evaluation of the effect of cord blood versus adult red blood cells on chromosomal breakage in Fanconi anemia.
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- Middle East Journal of Medical Genetics, 2015, v. 4, n. 1, p. 13, doi. 10.1097/01.MXE.0000456626.14919.1f
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- Article
Epilepsy and autistic manifestations in an Egyptian child with ring 14.
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- Middle East Journal of Medical Genetics, 2014, v. 3, n. 2, p. 65, doi. 10.1097/01.MXE.0000449830.77498.77
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- Article
Screening for common mutations in four FANCA gene exons in Egyptian Fanconi anemia patients.
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- Middle East Journal of Medical Genetics, 2014, v. 3, n. 1, p. 24, doi. 10.1097/01.MXE.0000438179.47299.3c
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- Article
Evaluation of the in-vitro protective effect of plant extract (astaxanthin) on chromosomal breakage in Fanconi anemia cell culture.
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- Middle East Journal of Medical Genetics, 2013, v. 2, n. 2, p. 45, doi. 10.1097/01.MXE.0000430775.91633.7f
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- Publication type:
- Article
Cytogenetic studies of chromosomal breakage diseases.
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- Middle East Journal of Medical Genetics, 2013, v. 2, n. 1, p. 11, doi. 10.1097/01.MXE.0000422776.59740.e2
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- Publication type:
- Article
Cytokinesis-blocked micronucleus assay in a group of Egyptian patients with Fanconi anemia.
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- Middle East Journal of Medical Genetics, 2012, v. 1, n. 2, p. 76, doi. 10.1097/01.MXE.0000414809.51187.d6
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- Article
A Homozygous Missense Mutation in FANCA Gene in a 46,XY Female with Gonadal Dysgenesis.
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- Sexual Development, 2018, v. 12, n. 5, p. 239, doi. 10.1159/000491407
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- Article
Expanding the mutation and clinical spectrum of Roberts syndrome.
- Published in:
- Congenital Anomalies, 2016, v. 56, n. 4, p. 154, doi. 10.1111/cga.12151
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- Publication type:
- Article
Modulation of miR-192/NF-κB/ TGF-β/ E-cadherin by thymoquinone protects against diethylnitrosamine /carbon tetrachloride hepatotoxicity.
- Published in:
- Physiology International, 2022, v. 109, n. 3, p. 371, doi. 10.1556/2060.2022.00163
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- Article
De Novo Mutation in ABCC9 Causes Hypertrichosis Acromegaloid Facial Features Disorder.
- Published in:
- Pediatric Dermatology, 2016, v. 33, n. 2, p. e109, doi. 10.1111/pde.12821
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- Article
Ectodermal Abnormalities in Patients with Kabuki Syndrome.
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- Pediatric Dermatology, 2011, v. 28, n. 5, p. 507, doi. 10.1111/j.1525-1470.2011.01495.x
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- Article
Relation between Arrogant Nursing Supervision and Work Effectiveness from Nurses' Prospective.
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- Tanta Scientific Nursing Journal, 2023, v. 31, p. 87, doi. 10.21608/tsnj.2023.328660
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- Article
Adult Living Donor Liver Re-Transplant Following Late Pediatric Liver Transplant Failure: A Case Report.
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- American Journal of Case Reports, 2019, v. 20, p. 908, doi. 10.12659/AJCR.914456
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- Article
Evaluation of circulating miRNAs and mRNAs expression patterns in autism spectrum disorder.
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- Egyptian Journal of Medical Human Genetics, 2021, v. 22, n. 1, p. 1, doi. 10.1186/s43042-021-00202-8
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- Article
Muenke syndrome with pigmentary disorder and probable hemimegalencephaly: An expansion of the phenotype.
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- American Journal of Medical Genetics. Part A, 2011, v. 155A, n. 1, p. 207, doi. 10.1002/ajmg.a.33777
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- Publication type:
- Article
Response to letter from Okoye JO and Ngokere AA "Are the prevalence of Trisomy 13 and the incidence of severe holoprosencephaly increasing in Africa?".
- Published in:
- Prenatal Diagnosis, 2020, v. 40, n. 12, p. 1618, doi. 10.1002/pd.5804
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- Article
Response to letter from Okoye JO and Ngokere AA "Are the prevalence of Trisomy 13 and the incidence of severe holoprosencephaly increasing in Africa?".
- Published in:
- Prenatal Diagnosis, 2020, v. 40, p. 1618, doi. 10.1002/pd.5804
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- Publication type:
- Article
Prenatal ultrasound findings of holoprosencephaly spectrum: Unusual associations.
- Published in:
- 2020
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- Publication type:
- journal article
Two Abnormal Cell Lines of Trisomy 14 and t(X;14) with Skewed X-Inactivation.
- Published in:
- Cytogenetic & Genome Research, 2020, v. 160, n. 3, p. 124, doi. 10.1159/000506430
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- Article
Bilateral Calcification of Basal Ganglia in a Patient with Duplication of Both 11q13.1q22.1 and 4q35.2 with New Phenotypic Features.
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- Cytogenetic & Genome Research, 2019, v. 159, n. 3, p. 130, doi. 10.1159/000504075
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- Article
Nursing Staff Perception Regarding Crises Management during Pandemics.
- Published in:
- Tanta Scientific Nursing Journal, 2024, v. 33, p. 245
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- Article
Nurses' Perception regarding Twelve Hour Shifts and Professionalism at Intensive Care Units.
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- Tanta Scientific Nursing Journal, 2024, v. 33, n. 2, p. 88, doi. 10.21608/tsnj.2024.350968
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- Article
Influence of Head Nurses' Exploitative Leadership Style on Nurses' Workplace Alienation.
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- Tanta Scientific Nursing Journal, 2024, v. 32, p. 169
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- Publication type:
- Article
Screening of the SHOX/PAR1 region using MLPA and miRNA expression profiling in a group of Egyptian children with non-syndromic short stature.
- Published in:
- Egyptian Journal of Medical Human Genetics, 2020, v. 21, n. 1, p. N.PAG, doi. 10.1186/s43042-020-00090-4
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- Article
Telomerase reverse transcriptase gene amplification in hematological malignancies.
- Published in:
- Egyptian Journal of Medical Human Genetics, 2019, v. 20, n. 1, p. N.PAG, doi. 10.1186/s43042-019-0036-z
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- Publication type:
- Article