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Articles related to 4076251 [Unique ID], provided by the PubMed system
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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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Hoekx J, Smeitink J, Brunner H, et al. 
[The De Barsy syndrome] [Case Reports, Journal Article]
Tijdschr Kindergeneeskd 1989 Apr; 57(2):53-7.
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Arazi M, Kapicioğlu MI, Mutlu M 
The de Barsy syndrome. [Case Reports, Journal Article]
Turk J Pediatr 2001 Jan-Mar; 43(1):79-84.
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Kivuva EC, Parker MJ, Cohen MC, et al. 
De Barsy syndrome: a review of the phenotype. [JOURNAL ARTICLE]
Clin Dysmorphol 2008 Apr; 17(2):99-107.
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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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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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Aldave AJ, Eagle RC, Streeten BW, et al. 
Congenital corneal opacification in De Barsy syndrome. [Case Reports, Journal Article]
Arch Ophthalmol 2001 Feb; 119(2):285-8.
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Baraitser M, Patton M, Lam ST, et al. 
The Angelman (Happy Puppet) syndrome: is it autosomal recessive? [Case Reports, Journal Article]
Clin Genet 1987 May; 31(5):323-30.
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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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