Found: 15
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Evaluation of Clinical Manifestations in Patients with Severe Lymphedema with and without CCBE1 Mutations.
- Published in:
- Molecular Syndromology, 2013, v. 4, n. 3, p. 107, doi. 10.1159/000342486
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- Publication type:
- Article
Ectodermal dysplasia: otolaryngologic manifestations and management.
- Published in:
- 2002
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- Publication type:
- Journal Article
To Evaluate the Feasibility of Neurotisation of Facial Nerve Branches with Ipsilateral Masseteric Nerve: An Anatomic Study.
- Published in:
- Journal of Clinical & Diagnostic Research, 2014, v. 8, n. 4, p. 4, doi. 10.7860/JCDR/2014/7708.4302
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- Publication type:
- Article
Practical considerations in the clinical application of whole-exome sequencing.
- Published in:
- Clinical Genetics, 2016, v. 89, n. 2, p. 173, doi. 10.1111/cge.12569
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- Publication type:
- Article
Additional evidence that PGAP1 loss of function causes autosomal recessive global developmental delay and encephalopathy.
- Published in:
- Clinical Genetics, 2015, v. 88, n. 6, p. 597, doi. 10.1111/cge.12581
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- Publication type:
- Article
The RBMX gene as a candidate for the Shashi X-linked intellectual disability syndrome.
- Published in:
- Clinical Genetics, 2015, v. 88, n. 4, p. 386, doi. 10.1111/cge.12511
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- Publication type:
- Article
Social cognitive training in adolescents with chromosome 22q11.2 deletion syndrome: feasibility and preliminary effects of the intervention.
- Published in:
- Journal of Intellectual Disability Research, 2015, v. 59, n. 10, p. 902, doi. 10.1111/jir.12192
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- Publication type:
- Article
A tale worth telling: the impact of the diagnosis experience on disclosure of genetic disorders.
- Published in:
- Journal of Intellectual Disability Research, 2015, v. 59, n. 5, p. 474, doi. 10.1111/jir.12151
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- Publication type:
- Article
Association of the family environment with behavioural and cognitive outcomes in children with chromosome 22q11.2 deletion syndrome.
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- Journal of Intellectual Disability Research, 2014, v. 58, n. 1, p. 31, doi. 10.1111/jir.12054
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- Publication type:
- Article
Social skills and associated psychopathology in children with chromosome 22q11.2 deletion syndrome: implications for interventions.
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- Journal of Intellectual Disability Research, 2012, v. 56, n. 9, p. 865, doi. 10.1111/j.1365-2788.2011.01477.x
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- Publication type:
- Article
Awareness and practice concerning oral cancer among Ayurveda and Homeopathy practitioners in Davangere District: A speciality-wise analysis.
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- Journal of Natural Science, Biology & Medicine, 2015, v. 6, n. 1, p. 116, doi. 10.4103/0976-9668.149104
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- Publication type:
- Article
Cognitive correlates of a functional COMT polymorphism in children with 22q11.2 deletion syndrome.
- Published in:
- Clinical Genetics, 2006, v. 69, n. 3, p. 234, doi. 10.1111/j.1399-0004.2006.00569.x
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- Publication type:
- Article
Ring chromosome 17: phenotype variation by deletion size.
- Published in:
- Clinical Genetics, 2003, v. 64, n. 4, p. 361, doi. 10.1034/j.1399-0004.2003.00146.x
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- Publication type:
- Article
Vascular ring leading to tracheoesophageal compression in a patient with Rubinstein-Taybi syndrome.
- Published in:
- Clinical Genetics, 1995, v. 48, n. 6, p. 324, doi. 10.1111/j.1399-0004.1995.tb04119.x
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- Publication type:
- Article
Factors related to the presentation of patients with thick primary melanomas.
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- Medical Journal of Australia, 1991, v. 154, n. 9, p. 583, doi. 10.5694/j.1326-5377.1991.tb121217.x
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- Publication type:
- Article