Found: 6
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Evaluating the use of parental reports to estimate health care resource utilization in children with suspected genetic disorders.
- Published in:
- Journal of Evaluation in Clinical Practice, 2018, v. 24, n. 2, p. 416, doi. 10.1111/jep.12876
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- Publication type:
- Article
Correction to: Genome-wide sequencing as a first-tier screening test for short tandem repeat expansions.
- Published in:
- 2021
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- Publication type:
- Correction Notice
De novo mutations in the SET nuclear proto‐oncogene, encoding a component of the inhibitor of histone acetyltransferases (INHAT) complex in patients with nonsyndromic intellectual disability.
- Published in:
- Human Mutation, 2018, v. 39, n. 7, p. 1014, doi. 10.1002/humu.23541
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- Publication type:
- Article
FOXP1 haploinsufficiency: Phenotypes beyond behavior and intellectual disability?
- Published in:
- American Journal of Medical Genetics. Part A, 2017, v. 173, n. 12, p. 3172, doi. 10.1002/ajmg.a.38462
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- Publication type:
- Article
Shortened consent forms for genome‐wide sequencing: Parent and provider perspectives.
- Published in:
- Molecular Genetics & Genomic Medicine, 2020, v. 8, n. 7, p. 1, doi. 10.1002/mgg3.1254
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- Publication type:
- Article
The Genomic Consultation Service: A clinical service designed to improve patient selection for genome‐wide sequencing in British Columbia.
- Published in:
- Molecular Genetics & Genomic Medicine, 2018, v. 6, n. 4, p. 592, doi. 10.1002/mgg3.410
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- Publication type:
- Article