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CPLANE1
Clinical and Genetic Characteristics and Prenatal Diagnosis of Patients
Universidade Estadual De Campinas Faculdade De
Molecular Genetic Studies of Inherited Cystic Kidney Disease in Oman
Novel Gene Discovery in Primary Ciliary Dyskinesia
Opportunities and Challenges for Molecular Understanding of Ciliopathies–The 100,000 Genomes Project
Multilocus Disease-Causing Genomic Variations for Mendelian Disorders: Role of Systematic Phenotyping and Implications on Genetic Counselling
Signatures of Adaptive Evolution in Platyrrhine Primate Genomes 5 6 Hazel Byrne*, Timothy H
2.04.107 Carrier Screening for Genetic Diseases Original Policy Date: February 1, 2017 Effective Date: January 1, 2020 Section: 2.0 Medicine Page: Page 1 of 24
Towards the Identification of Causal Genes and Contributing
Clinician-Centric Diagnosis of Rare Genetic Diseases: Performance of a Gene Pertinence Metric in Decision Support for Clinicians Michael M
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