Found: 16
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The 'tissue press': a new device to flatten fresh tissue during ex vivo confocal microscopy examination.
- Published in:
- Skin Research & Technology, 2017, v. 23, n. 1, p. 121, doi. 10.1111/srt.12293
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- Publication type:
- Article
A new highly penetrant form of obesity due to deletions on chromosome 16p11.2.
- Published in:
- Nature, 2010, v. 463, n. 7281, p. 671, doi. 10.1038/nature08727
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- Publication type:
- Article
New management of peri-ocular basal cell carcinoma using in vivo and ex vivo confocal microscopes.
- Published in:
- 2015
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- Publication type:
- Abstract
Adapting a dermatological multi‐laser fluorescent confocal microscope for ophthalmology applications.
- Published in:
- Acta Ophthalmologica (1755375X), 2012, v. 90, p. 0, doi. 10.1111/j.1755-3768.2012.T095.x
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- Publication type:
- Article
Fluorescence multi‐laser scanning microscopy of the cornea and ocular adnexa: a new era for functional confocal microscopy in ophthalmology.
- Published in:
- Acta Ophthalmologica (1755375X), 2012, v. 90, p. 0, doi. 10.1111/j.1755-3768.2012.4643.x
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- Publication type:
- Article
In vivo laser scanning microscopy of cornea, conjunctiva and ocular adnexa with a handheld dermatological laser‐scanning microscope: new perspectives.
- Published in:
- Acta Ophthalmologica (1755375X), 2012, v. 90, p. 0, doi. 10.1111/j.1755-3768.2012.4642.x
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- Publication type:
- Article
Coupling innovative imaging: in vivo multilaser confocal microscopy and ex vivo confocal Raman spectroscopy of cornea and skin in nephropathic cystinosis.
- Published in:
- Acta Ophthalmologica (1755375X), 2012, v. 90, p. 0, doi. 10.1111/j.1755-3768.2012.2237.x
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- Publication type:
- Article
Search for ReCQL4 mutations in 39 patients genotyped for suspected Rothmund-Thomson/Baller-Gerold syndromes.
- Published in:
- Clinical Genetics, 2015, v. 87, n. 3, p. 244, doi. 10.1111/cge.12361
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- Publication type:
- Article
Molecular findings and clinical data in a cohort of 150 patients with anophthalmia/microphthalmia.
- Published in:
- Clinical Genetics, 2014, v. 86, n. 4, p. 326, doi. 10.1111/cge.12275
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- Publication type:
- Article
Nager syndrome: confirmation of SF3B4 haploinsufficiency as the major cause.
- Published in:
- Clinical Genetics, 2014, v. 86, n. 3, p. 246, doi. 10.1111/cge.12259
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- Publication type:
- Article
Split hand/foot malformation with long-bone deficiency and BHLHA9 duplication: report of 13 new families.
- Published in:
- Clinical Genetics, 2014, v. 85, n. 5, p. 464, doi. 10.1111/cge.12219
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- Publication type:
- Article
Trisomy 7 mosaicism prenatally misdiagnosed and maternal uniparental disomy in a child with pigmentary mosaicism and Russell- Silver syndrome.
- Published in:
- Clinical Genetics, 2012, v. 81, n. 3, p. 265, doi. 10.1111/j.1399-0004.2010.01621.x
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- Publication type:
- Article
Hippocampal dysgenesis and variable neuropsychiatric phenotypes in patients with Bardet-Biedl syndrome underline complex CNS impact of primary cilia.
- Published in:
- Clinical Genetics, 2011, v. 80, n. 6, p. 523, doi. 10.1111/j.1399-0004.2011.01688.x
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- Publication type:
- Article
A GPHN point mutation leading to molybdenum cofactor deficiency.
- Published in:
- Clinical Genetics, 2011, v. 80, n. 6, p. 598, doi. 10.1111/j.1399-0004.2011.01709.x
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- Publication type:
- Article
Adams-Oliver syndrome: clinical description of a four-generation family and exclusion of five candidate genes.
- Published in:
- Clinical Genetics, 2006, v. 69, n. 1, p. 86, doi. 10.1111/j.1399-0004.2006.00552.x
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- Publication type:
- Article
Dermoscopy, confocal microscopy and optical coherence tomography for the diagnosis of bedbug infestation.
- Published in:
- Journal of the European Academy of Dermatology & Venereology, 2017, v. 31, n. 4, p. e203, doi. 10.1111/jdv.13956
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- Publication type:
- Article