Author:
Gucev Zoran S,Pop-Jordanova Nada,Dumalovska Gordana,Stomnaroska Orhideja,Zafirovski Gorgji,Tasic Velibor B
Publisher
Springer Science and Business Media LLC
Reference20 articles.
1. Lacassie Y, Sack GH, McKusick VA: An autosomal dominant form of arthrogryposis multiplex congenita (AMC) with unusual dermatoglyphics. (Abstract). Birth Defects Orig Art Ser. 1977, XIII (3B): 246-247.
2. Hall JG, Reed SD, Driscoll EP: Part 1. Amyoplasia: a common, sporadic condition with congenital contractures. Am J Med Genet. 1983, 15: 571-590. 10.1002/ajmg.1320150407.
3. Hall JG, Reed SD, Greene G: The distal arthrogryposes: delineation of new entities--review and nosologic discussion. Am J Med Genet. 1982, 11: 185-239. 10.1002/ajmg.1320110208.
4. Daentl DL, Berg BO, Layzer RB, Epstein CJ: A new familial arthrogryposis without weakness. Neurology. 1974, 24: 55-60.
5. Krakowiak PA, O'Quinn JR, Bohnsack JF, Watkins WS, Carey JC, Jorde LB, Bamshad M: A variant of Freeman-Sheldon syndrome maps to 11p15.5-pter. Am J Hum Genet. 1997, 60: 426-432.
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