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| First Page | Document Content | |
|---|---|---|
 Biology Cytogenetics Rare diseases Chromosomal abnormalities Cri du chat 5P Fryns Syndrome Chromosome 5 Monosomy Health Syndromes Genetics |
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Orphanet Journal of Rare Diseases BioMed Central | DOCX DocumentDocID: 1wwhs - View Document |
| DOCX DocumentDocID: 1wv76 - View Document |
| PDF DocumentDocID: 1w4hN - View Document |
| -Application for Renewal of RDMM Catalyst Grants This application is to be used by the Network’s Scientific Advisory Committee (SAC) to determine as to whether to provide an additional year of funding ($DocID: 1vceh - View Document |
| MULTISYSTEMIC RARE DISEASESDocID: 1v3AN - View Document |