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Articles related to 8500259 [Unique ID], provided by the PubMed system
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Kreuz FR, Wittwer BH 
Del(2q)--cause of the wrinkly skin syndrome? [Case Reports, Journal Article, Review]
Clin Genet 1993 Mar; 43(3):132-8.
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Casamassima AC, Wesson SK, Conlon CJ, et al. 
Wrinkly skin syndrome: phenotype and additional manifestations. [Case Reports, Journal Article, Review]
Am J Med Genet 1987 Aug; 27(4):885-93.
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Azuri J, Mizrachi A, Weintraub S, et al. 
Neurological involvement in a child with the wrinkly skin syndrome. [Case Reports, Journal Article, Review]
Am J Med Genet 1999 Jan 1; 82(1):31-3.
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Van Buggenhout G, Van Ravenswaaij-Arts C, Mc Maas N, et al. 
The del(2)(q32.2q33) deletion syndrome defined by clinical and molecular characterization of four patients. [Case Reports, Journal Article]
Eur J Med Genet 2005 Jul-Sep; 48(3):276-89.
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Ramer JC, Ladda RL, Frankel CA, et al. 
A review of phenotype-karyotype correlations in individuals with interstitial deletions of the long arm of chromosome 2. [Case Reports, Journal Article, Review]
Am J Med Genet 1989 Mar; 32(3):359-63.
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Prasher VP, Krishnan VH, Clarke DJ, et al. 
Deletion of chromosome 2 (p11-p13): case report and review. [Case Reports, Journal Article, Review]
J Med Genet 1993 Jul; 30(7):604-6.
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Rajab A, Kornak U, Budde BS, et al. 
Geroderma osteodysplasticum hereditaria and wrinkly skin syndrome in 22 patients from Oman. [JOURNAL ARTICLE]
Am J Med Genet A 2008 Mar 17.
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Al-Gazali LI, Sztriha L, Skaff F, et al. 
Gerodermia osteodysplastica and wrinkly skin syndrome: are they the same? [Case Reports, Journal Article]
Am J Med Genet 2001 Jul 1; 101(3):213-20.
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Kroes HY, Tuerlings JH, Hordijk R, et al. 
Another patient with an interstitial deletion of chromosome 9: case report and a review of six cases with del(9)(q22q32). [Journal Article, Review]
J Med Genet 1994 Feb; 31(2):156-8.
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