References

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Courtens W, Perlmutter N, Dan B, Vamos E. New syndrome or severe expression of Gordon syndrome? A case report. Clin Dysmorphol 1997; 6: 39-44 Donofrio P,Ayala F. Familial streblodactyly.Acta Derm Venerol 1983;63:361-3

Figuera LE, Ramirez-Duenas ML, Garcia-Cruz D,Villar V, Can-tu JM. Guadalajara camptodactyly syndrome type I: a corroborative family. Clin Genet 1993; 43:11-5 Goodman RM, Katznelson MB-M, Katznelson A. Campto-dactyly, with muscular hypoplasia, skeletal dysplasia, and abnormal palmar creases: Tel Hashomer camptodactyly syndrome. J Med Genet 1976; 13:136-41 Gordon H, Davies D, Berman MM. Camptodactyly, cleft palate and club foot: syndrome showing the autosomal-dominant pattern of inheritance. J Med Genet 1969; 6:266-74 Halal F, Fraser FC. Camptodactyly, cleft palate, and club foot (the Gordon syndrome): a report of a large pedigree. J Med Genet 1979; 16: 149-50 Hefner RA. Crooked little finger (minor streblomicrodactyly).

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Dupuytren's disease. Scand J Dent Res 1990; 98:457-60 Raphael SA, Blau EB, Zhang WH, Hsu SH. Analysis of a large kindred with Blau syndrome for HLA, autoimmunity, and sarcoidosis. Am J Dis Child 1993; 147: 842-8 Saini SK, Rose CD. Liver involvement in familial granuloma-tous arthritis (Blau syndrome). J Rheumatol 1996; 23: 396-9

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