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25. A new form of autosomal dominant limb-girdle muscular dystrophy (LGMD1G) with progressive fingers and toes flexion limitation maps to chromosome 4p21. Starling A, Kok F, Passos-Bueno MR, Vainzof M, Zatz M. Eur J Hum Genet; 2004 Dec; 12(12):1033-40. PubMed ID: 15367920 [Abstract] [Full Text] [Related]
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32. Another family with tricho-rhino-phalangeal syndrome type III (Sugio-Kajii syndrome). Nagai T, Nishimura G, Kasai H, Hasegawa T, Kato R, Ohashi H, Fukushima Y. Am J Med Genet; 1994 Feb 01; 49(3):278-80. PubMed ID: 8209886 [Abstract] [Full Text] [Related]
33. Short-rib-polydactyly syndrome (Saldino-Noonan type). Pirnar T, Balci S, Cağlar M. Turk J Pediatr; 1982 Feb 01; 24(3):175-82. PubMed ID: 7147365 [No Abstract] [Full Text] [Related]
34. [Rudimentary acral anomalies in a patient with Acrocal-losal syndrome]. Silengo M, Del Monaco A, Defilippi C. Radiol Med; 2001 Apr 01; 101(4):299-301. PubMed ID: 11398065 [No Abstract] [Full Text] [Related]
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