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3. Arthrogryposis, perthes disease, and upward gaze palsy: a novel autosomal recessive syndromic form of arthrogryposis. Alkuraya FS Am J Med Genet A; 2011 Feb; 155A(2):297-300. PubMed ID: 21271645 [TBL] [Abstract][Full Text] [Related]
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10. Familial distal arthrogryposis type I. Stoll C; Alembik Y; Dott B Ann Genet; 1996; 39(2):75-80. PubMed ID: 8766137 [TBL] [Abstract][Full Text] [Related]
11. Arthrogryposis multiplex congenita: a report of two cases. Brooks JG; Coster DJ Aust N Z J Ophthalmol; 1994 May; 22(2):127-32. PubMed ID: 7917267 [TBL] [Abstract][Full Text] [Related]
13. Distal arthrogryposis type II: a family with varying congenital abnormalities. Reiss JA; Sheffield LJ Am J Med Genet; 1986 Jun; 24(2):255-67. PubMed ID: 3717209 [TBL] [Abstract][Full Text] [Related]
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16. Mutations of GPR126 are responsible for severe arthrogryposis multiplex congenita. Ravenscroft G; Nolent F; Rajagopalan S; Meireles AM; Paavola KJ; Gaillard D; Alanio E; Buckland M; Arbuckle S; Krivanek M; Maluenda J; Pannell S; Gooding R; Ong RW; Allcock RJ; Carvalho ED; Carvalho MD; Kok F; Talbot WS; Melki J; Laing NG Am J Hum Genet; 2015 Jun; 96(6):955-61. PubMed ID: 26004201 [TBL] [Abstract][Full Text] [Related]
17. Arthrogryposis multiplex congenita--myopathic type. Lebenthal E; Ben-Bassat M; Reisner SH; Seelenfreund M Isr J Med Sci; 1973 Apr; 9(4):463-8. PubMed ID: 4709230 [No Abstract] [Full Text] [Related]
18. A dominantly inherited form of arthrogryposis multiplex congenita with unusual dermatoglyphics. Sack GH Clin Genet; 1978 Dec; 14(6):317-23. PubMed ID: 729196 [TBL] [Abstract][Full Text] [Related]
19. Arthrogryposis multiplex congenita associated with lissencephaly: a case report. Massa G; Casaer P; Ceulemans B; Van Eldere S Neuropediatrics; 1988 Feb; 19(1):24-6. PubMed ID: 3362309 [TBL] [Abstract][Full Text] [Related]
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