Works matching DE "ROBERTS syndrome"
Results: 16
Antenatal three-dimensional sonographic features of Roberts syndrome.
- Published in:
- 2011
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- Publication type:
- journal article
Roberts-SC Fokomeli Sendromu: Olgu Sunumu.
- Published in:
- 2012
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- Publication type:
- Case Study
A Case of Norman-Roberts Syndrome Identified from Postnatal Diagnosis of Microlissencephaly.
- Published in:
- Fetal & Pediatric Pathology, 2015, v. 34, n. 3, p. 197, doi. 10.3109/15513815.2015.1031414
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- Publication type:
- Article
Roberts-SC syndrome, a rare syndrome and cleft palate repair.
- Published in:
- Indian Journal of Plastic Surgery, 2008, v. 41, n. 2, p. 222, doi. 10.4103/0970-0358.44939
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- Publication type:
- Article
Long-term survival after corrective surgeries in two patients with severe deformities due to Roberts syndrome: A Case report and review of the literature.
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- Experimental & Therapeutic Medicine, 2018, v. 15, n. 2, p. 1702, doi. 10.3892/etm.2017.5592
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- Publication type:
- Article
Cohesinopathies of a Feather Flock Together.
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- PLoS Genetics, 2013, v. 9, n. 12, p. 1, doi. 10.1371/journal.pgen.1004036
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- Publication type:
- Article
Tetra-amelia with lung hypoplasia and facial clefts, Roberts-SC syndrome: report of two cases.
- Published in:
- 2010
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- Publication type:
- journal article
The non-redundant function of cohesin acetyltransferase Esco2.
- Published in:
- Nucleus (1949-1034), 2012, v. 3, n. 4, p. 1, doi. 10.4161/nucl.20440
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- Publication type:
- Article
3D-FISH analysis reveals chromatid cohesion defect during interphase in Roberts syndrome.
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- Molecular Cytogenetics (17558166), 2014, v. 7, n. 1, p. 1, doi. 10.1186/s13039-014-0059-6
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- Publication type:
- Article
ROBERTS-SC PHOCOMELIA SYNDROME: SPONTANEOUS OCCURRENCE IN NON THALIDOMIDE ERA: A RARE CASE WITH THE REVIEW OF LITERATURE AND MANAGEMENT ISSUES.
- Published in:
- 2013
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- Publication type:
- Case Study
FROM THE EDITOR'S DESK.
- Published in:
- Indian Obstetrics & Gynaecology, 2013, v. 3, n. 3, p. 5
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- Publication type:
- Article
A Zebrafish Model of Roberts Syndrome Reveals That Esco2 Depletion Interferes with Development by Disrupting the Cell Cycle.
- Published in:
- PLoS ONE, 2011, v. 6, n. 5, p. 1, doi. 10.1371/journal.pone.0020051
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- Publication type:
- Article
The Cellular Phenotype of Roberts Syndrome Fibroblasts as Revealed by Ectopic Expression of ESCO2.
- Published in:
- PLoS ONE, 2009, v. 4, n. 9, p. 1, doi. 10.1371/journal.pone.0006936
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- Publication type:
- Article
Roberts syndrome is caused by mutations in ESCO2, a human homolog of yeast ECO1 that is essential for the establishment of sister chromatid cohesion.
- Published in:
- Nature Genetics, 2005, v. 37, n. 5, p. 468, doi. 10.1038/ng1548
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- Publication type:
- Article
Improved transcription and translation with L-leucine stimulation of mTORC1 in Roberts syndrome.
- Published in:
- BMC Genomics, 2016, v. 17, p. 1, doi. 10.1186/s12864-015-2354-y
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- Publication type:
- Article
Shoulder joint replacement can improve quality of life and outcome in patients with dysmelia: a case series.
- Published in:
- 2016
- By:
- Publication type:
- journal article