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23. Band heterotopias: a newly recognized neuronal migration anomaly. Barkovich AJ; Jackson DE; Boyer RS Radiology; 1989 May; 171(2):455-8. PubMed ID: 2468173 [TBL] [Abstract][Full Text] [Related]
24. 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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28. Further evidence that arthrogryposis multiplex congenita in the human sometimes is caused by an intrauterine vascular accident. Robertson WL; Glinski LP; Kirkpatrick SJ; Pauli RM Teratology; 1992 Apr; 45(4):345-51. PubMed ID: 1533956 [TBL] [Abstract][Full Text] [Related]
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30. [Pachygyria and laminar heterotopic tissue. A rare case of unique expression of a neuronal migration disorder in twins]. Hebing B; Uhlenbrock D; Wesseler K Monatsschr Kinderheilkd; 1992 Apr; 140(4):220-2. PubMed ID: 1614447 [TBL] [Abstract][Full Text] [Related]
31. Arthrogryposis multiplex congenita and cerebellopontine ischemic lesions in sibs: recurrence of prenatal disruptive brain lesions with different patterns of expression? Mahieu-Caputo D; Salomon LJ; Dommergues M; Aubry MC; Sonigo P; Martinovic Y; Le Merrer M; Dumez Y; Encha-Razavi F Fetal Diagn Ther; 2002; 17(3):153-6. PubMed ID: 11914567 [TBL] [Abstract][Full Text] [Related]
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34. Arthrogryposis multiplex congenita and bilateral mid-brain infarction following maternal overdose of co-proxamol. Maalouf EF; Battin M; Counsell SJ; Rutherford MA; Manzur AY Eur J Paediatr Neurol; 1997; 1(5-6):183-6. PubMed ID: 10728216 [TBL] [Abstract][Full Text] [Related]
35. Grey matter heterotopia: an unusual association of intractable epilepsy. Stafford Johnson DB; Brennan P; Dwyer AJ; Toland J Ir J Med Sci; 1997; 166(3):135-8. PubMed ID: 9256546 [TBL] [Abstract][Full Text] [Related]
36. Recurrent de novo BICD2 mutation associated with arthrogryposis multiplex congenita and bilateral perisylvian polymicrogyria. Ravenscroft G; Di Donato N; Hahn G; Davis MR; Craven PD; Poke G; Neas KR; Neuhann TM; Dobyns WB; Laing NG Neuromuscul Disord; 2016 Nov; 26(11):744-748. PubMed ID: 27751653 [TBL] [Abstract][Full Text] [Related]
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