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Futreal PA

Mutations in the gene encoding capillary morphogenesis protein 2 cause juvenile hyaline fibromatosis and infantile systemic hyalinosis
Ehlers-Danlos syndrome with severe early-onset periodontal disease (EDS-VIII) is a distinct, heterogeneous disorder with one predisposition gene at chromosome 12p13
The gene for juvenile hyaline fibromatosis maps to chromosome 4q21
Confirmation of a gene locus for medullary cystic kidney disease (MCKD2) on chromosome 16p12
Localization of the gene for distal hereditary motor neuronopathy VII (dHMN-VII) to chromosome 2q14

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