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- Oligohydramnios Precision Panel Overview Indications Clinical Utility
- Mygenome Gene-Disease Reference List for Providers
- Ontology-Based Methods for Disease Similarity Estimation and Drug
- Ehlers-Danlos Syndrome Precision Panel Overview Indications
- Nuove Politiche Per L'innovazione Nel Settore Delle Scienze Della Vita
- Exome Sequencing Enhanced Package Department of Pathology and Laboratory Medicine Feb 2012 UCLA Molecular Diagnostics Laboratories Page:1
- Hereditary Disorders of Connective Tissue: a Guide to the Emerging Differential Diagnosis Maureen Murphy-Ryan, BS1, Apostolos Psychogios, MD2, and Noralane M
- FBN1 Gene Fibrillin 1
- Mendeliome Panel Versie V3 (4362 Genen) Centrum Voor Medische Genetica Gent
- Cardiac Next-Generation Sequencing Panels
- Chromosomal Abnormalities Chromosome Mutations/Anomalies / Diseases Number 1 1
- Stroke Panel 2019-01-31 Versie Centrum Voor Medische Genetica Gent (102 Genen)
- WES Gene Package Multiple Congenital Anomalie
- Cardiopathy Panel Versie V5 (168 Genen) Centrum Voor Medische Genetica Gent
- Fabio Pammolli, Massimo Riccaboni, Laura Magazzini, Mark Supekar
- Signalling Defects and Disease 12 1
- Ventriculomegaly Precision Panel Overview Indications Clinical Utility
- ACMG Actionable Diseases Precision Panel Overview Indications
- Stickler Syndrome Precision Panel Overview Indications Clinical Utility
- WES Gene Package Multiple Congenital Anomalie
- Marfan Syndrome, Diagnostics and Life Status in Adults
- Blueprint Genetics Marfan Syndrome Panel
- Individual Genome Sequence Gene List (By Disease)
- Duke University Dissertation Template
- Characterization of Two Novel Intronic Variants Affecting Splicing in FBN1
- Leistungsverzeichnis Der Sektion Pädiatrische Genetik Der Universitätskinderklinik Freiburg, Mathildenstr
- Signalling Defects and Disease 12 1
- Cellular Processes 7 1
- FBN1-Specific Polyclonal ANTIBODY Catalog Number:20251-1-AP
- Blueprint Genetics Ectopia Lentis Panel
- OMIM Mendelian Gene List V2.0
- The New Ghent Criteria for Marfan Syndrome: What Do They Change? G Faivre, Gwenaëlle Collod-Béroud, a Adès, a Arbustini, C Child, C Callewaert, B Loeys, C
- Recessive Gene List V2.0
- Genetic Diagnostics Test(S)/Gene(S)/Panel(S)
- Disease ID Disorder Name Gene Symbols OMIM ID