共 68 条
[1]
Wang YY(2011)A novel splice site mutation in ANTXR2 (CMG2) gene results in systemic hyalinosis J Pediatr Hematol Oncol 33 355-357
[2]
Wen CQ(2003)Mutations in the gene encoding capillary morphogenesis protein 2 cause juvenile hyaline fibromatosis and infantile systemic hyalinosis Am J Hum Genet 73 791-800
[3]
Wei Z(2003)Mutations in capillary morphogenesis gene-2 result in the allelic disorders juvenile hyaline fibromatosis and infantile systemic hyalinosis Am J Hum Genet 73 957-966
[4]
Jin X(2009)Juvenile hyaline fibromatosis and infantile systemic hyalinosis: a unifying term and a proposed grading system J Am Acad Dermatol 61 695-700
[5]
Hanks S(2012)Identification of 2 novel ANTXR2 mutations in patients with hyaline fibromatosis syndrome and proposal of a modified grading system Am J Med Genet A 158A 732-742
[6]
Adams S(1999)Juvenile hyaline fibromatosis: clinical heterogeneity in three patients Dermatology 198 18-25
[7]
Douglas J(1986)Infantile systemic hyalinosis: report of four cases of a disease, fatal in infancy, apparently different from juvenile systemic hyalinosis Paediatr Pathol 6 55-79
[8]
Dowling O(2010)Clinical and imaging findings of systemic hyalinosis: two cases presenting with congenital arthrogryposis Skelet Radiol 39 589-593
[9]
Difeo A(2008)Infantile systemic hyalinosis: case report and review of the literature J Am Acad Dermatol 58 303-307
[10]
Ramirez MC(2011)Juvenile hyaline fibromatosis: focus on radiographic features in adulthood Rheumatol Int 31 273-276