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28. X-linked recessive inheritance of dysgenesis of corpus callosum in a Chinese family. Kang WM; Huang CC; Lin SJ Am J Med Genet; 1992 Nov; 44(5):619-23. PubMed ID: 1481821 [TBL] [Abstract][Full Text] [Related]
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31. Microcephaly-lymphedema-chorioretinal dysplasia associated with pachymicrogyria and atrophy of the cerebellar vermis: an integration of brain-ocular migration disorders. Pastora N; Peralta J; Canal-Fontcuberta I; Grabowska A; Pulido JS; Abelairas J; Armada F; Garcia-Alix A Ophthalmic Genet; 2012 Jun; 33(2):116-8. PubMed ID: 22420539 [TBL] [Abstract][Full Text] [Related]
32. Postnatal short stature, microcephaly, severe syndactyly of hands and feet, dysmorphic face, and mental retardation: a new syndrome? Zerres K; Rietschel M; Rietschel E; Majewski F; Meinecke P J Med Genet; 1992 Apr; 29(4):269-71. PubMed ID: 1316441 [TBL] [Abstract][Full Text] [Related]
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34. Autosomal recessive microcephaly with early onset seizures and spasticity. Silengo M; Lerone M; Martinelli M; Martucciello G; Caffarena PE; Jasonni V; Romeo G Clin Genet; 1992 Sep; 42(3):152-5. PubMed ID: 1395086 [TBL] [Abstract][Full Text] [Related]
35. Electroretinograms in microcephaly with chorioretinal degeneration. Manning FJ; Bruce AM; Berson EL Am J Ophthalmol; 1990 Apr; 109(4):457-63. PubMed ID: 2330949 [TBL] [Abstract][Full Text] [Related]
36. Syndrome of microcephaly, deafness/malformed ears, mental retardation and peculiar facies in a mother and son. Kawashima H; Tsuji N Clin Genet; 1987 May; 31(5):303-7. PubMed ID: 3608216 [TBL] [Abstract][Full Text] [Related]
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39. Unknown syndrome. A possible new X linked retardation syndrome: dysmorphic facies, microcephaly, hypotonia, and small genitalia. Porteous ME; Burn J J Med Genet; 1990 May; 27(5):339-40. PubMed ID: 2352265 [TBL] [Abstract][Full Text] [Related]