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Robertson SP, Bankier A 
Sotos syndrome and cutis laxa. [Case Reports, Journal Article]
J Med Genet 1999 Jan; 36(1):51-6.
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Morava E, Lefeber DJ, Urban Z, et al. 
Defining the phenotype in an autosomal recessive cutis laxa syndrome with a combined congenital defect of glycosylation. [JOURNAL ARTICLE]
Eur J Hum Genet 2007 Oct 31.
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Fryns JP, Vogels A, Haegeman J, et al. 
Costello syndrome: a postnatal growth retardation syndrome with distinct phenotype. [Case Reports, Journal Article]
Genet Couns 1994; 5(4):337-43.
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Gupta N, Phadke SR 
Cutis Laxa Type II and Wrinkly Skin Syndrome: Distinct Phenotypes. [Journal Article]
Pediatr Dermatol 2006 May-Jun; 23(3):225-30.
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Morava E, Wopereis S, Coucke P, et al. 
Defective protein glycosylation in patients with cutis laxa syndrome. [Case Reports, Journal Article]
Eur J Hum Genet 2005 Apr; 13(4):414-21.
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Imaizumi K, Kurosawa K, Makita Y, et al. 
Male with type II autosomal recessive cutis laxa. [Case Reports, Journal Article]
Clin Genet 1994 Jan; 45(1):40-3.
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Hucthagowder V, Sausgruber N, Kim KH, et al. 
Fibulin-4: a novel gene for an autosomal recessive cutis laxa syndrome. [Journal Article]
Am J Hum Genet 2006 Jun; 78(6):1075-80.
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Koppe R, Kaplan P, Hunter A, et al. 
Ambiguous genitalia associated with skeletal abnormalities, cutis laxa, craniostenosis, psychomotor retardation, and facial abnormalities (SCARF syndrome). [Case Reports, Journal Article]
Am J Med Genet 1989 Nov; 34(3):305-12.
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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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