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Bartsocas CS, Dimitriou J, Kavadias A, et al. 
De Barsy syndrome. [Case Reports, Journal Article]
Prog Clin Biol Res 1982.:157-60.
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Kunze J, Majewski F, Montgomery P, et al. 
De Barsy syndrome--an autosomal recessive, progeroid syndrome. [Journal Article]
Eur J Pediatr 1985 Nov; 144(4):348-54.
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Young ID, Moore JR 
Intrafamilial variation in Cohen syndrome. [Journal Article]
J Med Genet 1987 Aug; 24(8):488-92.
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Nelson J, Flaherty M, Grattan-Smith P 
Gillespie syndrome: a report of two further cases. [Case Reports, Journal Article]
Am J Med Genet 1997 Aug 8; 71(2):134-8.
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Burn J, Martin N 
Two retarded male cousins with odd facies, hypotonia, and severe constipation: possible examples of the X linked FG syndrome. [Case Reports, Journal Article]
J Med Genet 1983 Apr; 20(2):97-9.
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Antiñolo G, Rufo M, Borrego S, et al. 
Megalocornea-mental retardation syndrome: an additional case. [Case Reports, Journal Article, Review]
Am J Med Genet 1994 Aug 15; 52(2):196-7.
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Yomo A, Taira T, Kondo I 
Goldberg-Shprintzen syndrome: Hirschsprung disease, hypotonia, and ptosis in sibs. [Case Reports, Journal Article, Review]
Am J Med Genet 1991 Nov 1; 41(2):188-91.
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Dallapiccola B, Zelante L, Cristalli P 
Diagnostic definition of the FG syndrome. [Case Reports, Letter]
Am J Med Genet 1984 Oct; 19(2):379-81.
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Gazit E, Goodman RM, Katznelson MB, et al. 
The Wrinkly Skin Syndrome: a new heritable disorder of connective tissue. [Journal Article]
Clin Genet 1973; 4(3):186-92.
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