Congenital gastrointestinal defects in Down syndrome - Emory ...
Creating genetic reports that are understood by nonspecialists: a case study | Genetics in Medicine
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Example Genome Report result summary. | Download Scientific Diagram
A report template for molecular genetic tests designed to improve communication between the clinician and laboratory. | Semantic Scholar
Table of contents | Journal of Medical Genetics
Journal of Clinical Genetics and Genomics | Open Access Journals
Genetic predictors of cardiovascular morbidity in Bardet-Biedl syndrome – topic of research paper in Clinical medicine. Download scholarly article PDF and read for free on CyberLeninka open science hub.
Journal of Medical Genetics - A leading BMJ journal for geneticists
Clinical Genetics
Recommendations for designing genetic test reports to be understood by patients and non-specialists | European Journal of Human Genetics
Developing patient-friendly genetic and genomic test reports: formats to promote patient engagement and understanding | Genome Medicine | Full Text
PDF) Clinical and molecular characterization of individuals with recurrent genomic disorder at 10q22.3q23.2 | Sarah Dyack - Academia.edu
Return of genetic and genomic research findings: experience of a pediatric biorepository | BMC Medical Genomics | Full Text
Identification of critical regions for clinical features of distal 10q deletion syndrome
Clinical Genetics Research Papers - Academia.edu
PDF) Expanding the phenotypic spectrum of ECEL1 -related congenital contracture syndromes | Caroline Andrews and Sherin Shaaban - Academia.edu
Clinical Genetics - Wiley Online Library
Clinical Genetics - Wiley Online Library
Creating genetic reports that are understood by nonspecialists: a case study | Genetics in Medicine
A rare cause of short stature: Kenny-Caffey syndrome type 2 – a case report and literature review
PDF) A Report Template for Molecular Genetic Tests Designed to Improve Communication Between the Clinician and Laboratory
Dystrophic epidermolysis bullosa pruriginosa in ... - ResearchGate
Stüve-Wiedemann syndrome: long-term follow-up and genetic heterogeneity | Andre Megarbane - Academia.edu
Featured Cover - Rezaei - 2021 - Clinical Genetics - Wiley Online Library
Clinical Genetics - Wiley Online Library
