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Wilms Tümörü: Tek Merkezin 32 Yıllık Deneyimleri ile Güncel Literatürün Gözden Geçirilmesi.
- Published in:
- Medical Journal of Istanbul Kanuni Sultan Süleyman / İstanbul Kanuni Sultan Süleyman Tıp Dergisi, 2021, v. 13, n. 3, p. 207, doi. 10.4274/iksstd.2021.81557
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- Publication type:
- Article
Giant benign lymphangioendothelioma.
- Published in:
- Journal of Cutaneous Pathology, 2012, v. 39, n. 10, p. 950, doi. 10.1111/j.1600-0560.2012.01971.x
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- Publication type:
- Article
A submicroscopic deletion of 11p13 associated with the WAGR syndrome.
- Published in:
- Clinical Genetics, 2003, v. 63, n. 4, p. 319, doi. 10.1034/j.1399-0004.2003.00051.x
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- Article
Potocki‐Shaffer syndrome revealed in a WAGR syndrome case with multiple exostoses.
- Published in:
- 2023
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- Publication type:
- Case Study
Congenital Bilateral Aniridia with Ectopia Lentis: A Case Report.
- Published in:
- Journal of Clinical & Diagnostic Research, 2024, v. 18, n. 3, p. 1, doi. 10.7860/JCDR/2024/66990.19177
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- Publication type:
- Article
Sustained endocrine profiles of a girl with WAGR syndrome.
- Published in:
- 2017
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- Publication type:
- Case Study
Correction: The WAGR syndrome gene PRRG4 is a functional homologue of the commissureless axon guidance gene.
- Published in:
- 2017
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- Publication type:
- Correction Notice
The WAGR syndrome gene PRRG4 is a functional homologue of the commissureless axon guidance gene.
- Published in:
- PLoS Genetics, 2017, v. 13, n. 8, p. 1, doi. 10.1371/journal.pgen.1006865
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- Publication type:
- Article
WT1-related disorders: more than Denys-Drash syndrome.
- Published in:
- Pediatric Nephrology, 2024, v. 39, n. 9, p. 2601, doi. 10.1007/s00467-024-06302-y
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- Publication type:
- Article
Correction to: Risk factors for post-nephrectomy hypotension in pediatric patients.
- Published in:
- 2021
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- Publication type:
- Correction Notice
Risk factors for post-nephrectomy hypotension in pediatric patients.
- Published in:
- Pediatric Nephrology, 2021, v. 36, n. 11, p. 3699, doi. 10.1007/s00467-021-05115-7
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- Article
Lipid Metabolic Reprogramming in Embryonal Neoplasms with MYCN Amplification.
- Published in:
- Cancers, 2023, v. 15, n. 7, p. 2144, doi. 10.3390/cancers15072144
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- Publication type:
- Article
Clinical utility gene card for: WAGR syndrome.
- Published in:
- European Journal of Human Genetics, 2011, v. 19, n. 4, p. 1, doi. 10.1038/ejhg.2010.220
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- Publication type:
- Article
Nephroblastoma-specific dysregulated gene SNHG15 with prognostic significance: scRNA-Seq with bulk RNA-Seq data and experimental validation.
- Published in:
- Discover Oncology, 2024, v. 15, n. 1, p. 1, doi. 10.1007/s12672-024-00946-w
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- Article
WAGR syndrome in a Nepalese male child.
- Published in:
- 2016
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- Publication type:
- Case Study
A Rare Case With Aniridic Fibrosis Syndrome After Iris Diaphragm Intraocular Lens and Ahmed Valve Implantation in a Patient With WAGR Syndrome.
- Published in:
- 2017
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- Publication type:
- Case Study
Neuronal expression in Drosophila of an evolutionarily conserved metallophosphodiesterase reveals pleiotropic roles in longevity and odorant response.
- Published in:
- PLoS Genetics, 2023, v. 19, n. 9, p. 1, doi. 10.1371/journal.pgen.1010962
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- Publication type:
- Article
Dysgerminoma developing from an ectopic ovary in a patient with WAGR syndrome: A case report.
- Published in:
- 2016
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- Publication type:
- Case Study
Bilateral Peters' anomaly, aniridia and Wilms tumour (WAGR syndrome) in monozygotic twins.
- Published in:
- Acta Paediatrica, 2024, v. 113, n. 6, p. 1420, doi. 10.1111/apa.17160
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- Publication type:
- Article
Management of bilateral Wilms tumours.
- Published in:
- 2017
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- Publication type:
- journal article
Improving molecular diagnosis of aniridia and WAGR syndrome using customized targeted array-based CGH.
- Published in:
- PLoS ONE, 2017, v. 12, n. 2, p. 1, doi. 10.1371/journal.pone.0172363
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- Publication type:
- Article
A case of WAGR syndrome in association with developmental glaucoma requiring bilateral Baerveldt glaucoma implants and subsequent tube repositioning.
- Published in:
- Clinical Ophthalmology, 2015, v. 9, p. 1081, doi. 10.2147/OPTH.S80444
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- Publication type:
- Article
Conventional and molecular cytogenetic characterization of a Moroccan patient with WAGR syndrome.
- Published in:
- Egyptian Journal of Medical Human Genetics, 2024, v. 25, n. 1, p. 1, doi. 10.1186/s43042-024-00514-5
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- Publication type:
- Article
Prenatal Diagnosis of WAGR Syndrome.
- Published in:
- Case Reports in Obstetrics & Gynecology, 2015, p. 1, doi. 10.1155/2015/928585
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- Publication type:
- Article
Epidemiology of PAX6 Gene Pathogenic Variants and Expected Prevalence of PAX6 -Associated Congenital Aniridia across the Russian Federation: A Nationwide Study.
- Published in:
- Genes, 2023, v. 14, n. 11, p. 2041, doi. 10.3390/genes14112041
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- Publication type:
- Article
Complex Chromosomal Rearrangement Involving Chromosomes 10 and 11, Accompanied by Two Adjacent 11p14.1p13 and 11p13p12 Deletions, Identified in a Patient with WAGR Syndrome.
- Published in:
- 2023
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- Publication type:
- Case Study
Characterization of 11p14-p12 deletion in WAGR syndrome by array CGH for identifying genes contributing to mental retardation and autism.
- Published in:
- Cytogenetic & Genome Research, 2008, v. 122, n. 2, p. 181, doi. 10.1159/000172086
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- Publication type:
- Article
Pineal hypoplasia, reduced melatonin and sleep disturbance in patients with PAX6 haploinsufficiency.
- Published in:
- Journal of Sleep Research, 2016, v. 25, n. 1, p. 16, doi. 10.1111/jsr.12345
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- Publication type:
- Article
Anaesthetic management for a patient with WAGR syndrome.
- Published in:
- Anaesthesia, 2001, v. 56, n. 12, p. 1203, doi. 10.1046/j.1365-2044.2001.02369-24.x
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- Publication type:
- Article