Found: 7
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Delineation of MidXq28‐duplication syndrome distal to MECP2 and proximal to RAB39B genes.
- Published in:
- Clinical Genetics, 2019, v. 96, n. 3, p. 246, doi. 10.1111/cge.13565
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- Publication type:
- Article
Assessment of Crohn's disease in the small bowel: Prospective comparison of magnetic resonance enteroclysis with conventional enteroclysis.
- Published in:
- 2006
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- Publication type:
- journal article
Acute diverticulitis: beyond the diagnosis: predictive role of CT in assessing risk of recurrence and clinical implications in non-operative management of acute diverticulitis.
- Published in:
- La Radiologia Medica, 2024, v. 129, n. 8, p. 1118, doi. 10.1007/s11547-024-01841-8
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- Publication type:
- Article
Correction to: Chest CT for early detection and management of coronavirus disease (COVID-19): a report of 314 patients admitted to Emergency Department with suspected pneumonia.
- Published in:
- 2021
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- Publication type:
- Correction Notice
Chest CT for early detection and management of coronavirus disease (COVID-19): a report of 314 patients admitted to Emergency Department with suspected pneumonia.
- Published in:
- La Radiologia Medica, 2020, v. 125, n. 10, p. 931, doi. 10.1007/s11547-020-01256-1
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- Publication type:
- Article
Tremor is a major feature of 9p13 deletion syndrome.
- Published in:
- American Journal of Medical Genetics. Part A, 2020, v. 182, n. 11, p. 2694, doi. 10.1002/ajmg.a.61807
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- Publication type:
- Article
A novel mutation in CDH11, encoding cadherin‐11, cause Branchioskeletogenital (Elsahy‐Waters) syndrome.
- Published in:
- American Journal of Medical Genetics. Part A, 2018, v. 176, n. 9, p. 2028, doi. 10.1002/ajmg.a.40379
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- Publication type:
- Article