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26. Morphometric measurements of the cranium in patients with Chiari type I malformation and comparison with the normal population. Karagöz F; Izgi N; Kapíjcíjoğlu Sencer S Acta Neurochir (Wien); 2002 Feb; 144(2):165-71; discussion 171. PubMed ID: 11862517 [TBL] [Abstract][Full Text] [Related]
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28. A boy with a sac-like protrusion at the occipital region. Zhou YH; Zheng MH BMJ; 2016 Apr; 353():i2073. PubMed ID: 27079497 [No Abstract] [Full Text] [Related]
29. Dandy-Walker syndrome together with occipital encephalocele. Cakmak A; Zeyrek D; Cekin A; Karazeybek H Minerva Pediatr; 2008 Aug; 60(4):465-8. PubMed ID: 18511899 [TBL] [Abstract][Full Text] [Related]
30. Congenital hereditary cranium bifidum occultum frontalis with a review of anatomical variations in lower medsagittal region of frontal bones. TERRAFRANCA RJ; ZELLIS A Radiology; 1953 Jul; 61(1):60-6. PubMed ID: 13064405 [No Abstract] [Full Text] [Related]
31. [Occipital encephalocele with cerebellar dysontogenesis (at birth and 10 years later)]. Bignardi C; Zini GC; Provvisionato G Chir Organi Mov; 1978; 64(5):509-22. PubMed ID: 754913 [No Abstract] [Full Text] [Related]
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33. Spectrum of anomalies in the Meckel syndrome, or: "Maybe there is a malformation syndrome with at least one constant anomaly". Fraser FC; Lytwyn A Am J Med Genet; 1981; 9(1):67-73. PubMed ID: 7246621 [TBL] [Abstract][Full Text] [Related]
34. [Intracranial occipital hyperostosis with cerebellar syndrome]. POGGIALI A Riv Sper Freniatr Med Leg Alien Ment; 1951 Dec; 75(4):507-31. PubMed ID: 14930679 [No Abstract] [Full Text] [Related]
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36. Polydactyly in a carrier of the gene for the Meckel syndrome. Nelson J; Nevin NC; Hanna EJ Am J Med Genet; 1994 Nov; 53(3):207-9. PubMed ID: 7856653 [TBL] [Abstract][Full Text] [Related]
38. von Voss-Cherstvoy syndrome: a variable perinatally lethal syndrome of multiple congenital anomalies. Lubinsky MS; Kahler SG; Speer IE; Hoyme HE; Kirillova IA; Lurie IW Am J Med Genet; 1994 Sep; 52(3):272-8. PubMed ID: 7810558 [TBL] [Abstract][Full Text] [Related]
39. Autosomal recessive congenital cerebellar hypoplasia and short stature in a large inbred family. Mégarbané A; Delague V; Salem N; Loiselet J Am J Med Genet; 1999 Nov; 87(1):88-90. PubMed ID: 10528257 [No Abstract] [Full Text] [Related]