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- Conclusions from a Kidney Disease: Improving Global Outcomes
- Genomeposter2009.Pdf
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- Beacon Carrier Screening Detecting 400+ Conditions
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- WO 2016/014781 Al 28 January 2016 (28.01.2016) P O P C T
- Expert Guidelines for the Management of Alport Syndrome and Thin Basement Membrane Nephropathy
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- Smooth Muscle Tumors Associated with X-Linked Alport Syndrome: Carrier Detection in Females
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- Male-To-Male Transmission of X-Linked Alport Syndrome in a Boy with a 47,XXY Karyotype
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- Expert Guidelines for the Management of Alport Syndrome and TBMN 1Judy Savige, 2Martin Gregory, 3Oliver Gross, 4Clifford Kashtan, 5Jie Ding and 6Frances Flinter
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- Alport Syndrome Alport Syndrome Is an Inherited Disease That Affects a Part of the Kidney Called the Glomerulus
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- Knowledge Is Power. Plan Ahead with Geneaware. Gain the Knowledge Needed to Provide Your Patients Empowered Family Planning Decisions
- Alport Syndrome Aminoglycoside-Induced Deafness
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- Mutations in the COL4A5 Gene in Alport Syndrome: a Possible Mutation in Primordial Germ Cells
- Download Gene List
- X Linked Dominant Diseases Example
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- Kidneyseq™ Version 3 Gene List Iowa Institute of Human Genetics
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- PGT-M Disease List
- 17 X Chromosome Rearrangements
- Esit Diagnosis List
- Congenital Nephropathy Associated with Hearing Loss, Ocular Abnormalities, Mental Retardation, Convulsions and Abnormal E
- Alport's Syndrome
- Recessive Gene List V2.0
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- Maternal Genetic Disease. Edited by NB Isada, a Drugan, MP Johnson