Found: 13
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Tongue Part Movement Trajectories for /r/ Using Ultrasound.
- Published in:
- Perspectives of the ASHA Special Interest Groups, 2019, v. 4, n. 6, p. 1644, doi. 10.1044/2019_PERS-19-00064
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- Publication type:
- Article
Delineation of the 9q31 deletion syndrome: Genomic microarray characterization of two patients with overlapping deletions.
- Published in:
- American Journal of Medical Genetics. Part A, 2018, v. 176, n. 12, p. 2901, doi. 10.1002/ajmg.a.40664
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- Publication type:
- Article
Neuroradiographic findings in 22q11.2 deletion syndrome.
- Published in:
- American Journal of Medical Genetics. Part A, 2017, v. 173, n. 8, p. 2158, doi. 10.1002/ajmg.a.38304
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- Publication type:
- Article
7q11.23 Duplication Syndrome: Physical Characteristics and Natural History.
- Published in:
- American Journal of Medical Genetics. Part A, 2015, v. 167A, n. 12, p. 2916, doi. 10.1002/ajmg.a.37340
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- Publication type:
- Article
New recessive truncating mutation in LTBP3 in a family with oligodontia, short stature, and mitral valve prolapse.
- Published in:
- American Journal of Medical Genetics. Part A, 2015, v. 167A, n. 6, p. 1396, doi. 10.1002/ajmg.a.37049
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- Publication type:
- Article
Ectopia lentis as the presenting and primary feature in Marfan syndrome.
- Published in:
- American Journal of Medical Genetics. Part A, 2011, v. 155A, n. 11, p. 2661, doi. 10.1002/ajmg.a.34245
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- Publication type:
- Article
Using Children's Artifacts to Avoid Interpretive Missteps.
- Published in:
- Legacy (National Association for Interpretation), 2016, v. 27, n. 4, p. 24
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- Publication type:
- Article
Bilateral exudative retinal detachments and associated choroidal detachments in a patient on dapsone: a case report.
- Published in:
- International Journal of Retina & Vitreous, 2022, v. 8, n. 1, p. 1, doi. 10.1186/s40942-022-00383-3
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- Publication type:
- Article
Clinical and molecular cytogenetic characterization of a novel 10q interstitial deletion: a case report and review of the literature.
- Published in:
- Molecular Cytogenetics (17558166), 2019, v. 12, n. 1, p. N.PAG, doi. 10.1186/s13039-019-0430-8
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- Publication type:
- Article
The molecular and phenotypic spectrum of IQSEC2-related epilepsy.
- Published in:
- Epilepsia (Series 4), 2016, v. 57, n. 11, p. 1858, doi. 10.1111/epi.13560
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- Article
A recurrent mutation in KCNA2 as a novel cause of hereditary spastic paraplegia and ataxia.
- Published in:
- 2016
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- Publication type:
- journal article
A Qualitative Analysis of Clinician Perspectives of Ultrasound Biofeedback for Speech Sound Disorders.
- Published in:
- American Journal of Speech-Language Pathology, 2023, v. 32, n. 3, p. 1252, doi. 10.1044/2023_AJSLP-22-00194
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- Publication type:
- Article
Deletion at an 1q24 locus reveals a critical role of long noncoding RNA DNM3OS in skeletal development.
- Published in:
- Cell & Bioscience, 2021, v. 11, n. 1, p. 1, doi. 10.1186/s13578-021-00559-8
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- Publication type:
- Article