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82. [Weill-Marchesani syndrome. Study of a case]. Jouhaud F; Augustin P; Malbrel C Bull Soc Ophtalmol Fr; 1984 Oct; 84(10):1107-11. PubMed ID: 6544165 [No Abstract] [Full Text] [Related]
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84. Septo-optic dysplasia in two siblings. Benner JD; Preslan MW; Gratz E; Joslyn J; Schwartz M; Kelman S Am J Ophthalmol; 1990 Jun; 109(6):632-7. PubMed ID: 2346191 [TBL] [Abstract][Full Text] [Related]
85. [Computed tomography appearance of agenesis of the corpus callosum. A report of 5 cases (author's transl)]. Coursault R; Delouvrier JJ; Desbleds MT; Marsault C; Nahum H J Radiol; 1981 Feb; 62(2):103-6. PubMed ID: 7252897 [No Abstract] [Full Text] [Related]
86. Agenesis of the corpus callosum in Schinzel-Giedion syndrome associated with 47,XXY karyotype. Ozkinay FF; Akisü M; Kültürsay N; Oral R; Tansug N; Sapmaz G Clin Genet; 1996 Sep; 50(3):145-8. PubMed ID: 8946113 [TBL] [Abstract][Full Text] [Related]
87. Chondrodysplasia punctata with retinal colobomas: radiographic findings. Herman TE J Perinatol; 1998; 18(2):152-5. PubMed ID: 9605308 [No Abstract] [Full Text] [Related]
88. The acrocallosal syndrome in a Turkish boy. Yüksel M; Caliskan M; Oğur G; Ozmen M; Dolunay G; Apak S J Med Genet; 1990 Jan; 27(1):48-9. PubMed ID: 2308155 [TBL] [Abstract][Full Text] [Related]
89. Acrocallosal syndrome in a girl born to consanguineous parents. Salgado LJ; Ali CA; Castilla EE Am J Med Genet; 1989 Mar; 32(3):298-300. PubMed ID: 2729348 [TBL] [Abstract][Full Text] [Related]
90. The normal, absent, and abnormal corpus callosum: sonographic findings. Babcock DS Radiology; 1984 May; 151(2):449-53. PubMed ID: 6709917 [TBL] [Abstract][Full Text] [Related]
91. Provisionally unique autosomal recessive chondrodysplasia punctata syndrome. Toriello HV; Higgins JV; Miller T Am J Med Genet; 1993 Oct; 47(5):797-9. PubMed ID: 8267015 [TBL] [Abstract][Full Text] [Related]
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93. Evidence for possible Mendelian inheritance of septo-optic dysplasia. Wales JK; Quarrell OW Acta Paediatr; 1996 Mar; 85(3):391-2. PubMed ID: 8696006 [TBL] [Abstract][Full Text] [Related]
96. Previously undescribed syndrome of craniofacial, hand anomalies, and sensorineural deafness. Sommer A; Young-Wee T; Frye T Am J Med Genet; 1983 May; 15(1):71-7. PubMed ID: 6859126 [TBL] [Abstract][Full Text] [Related]
97. Cat's eye syndrome with cleft soft palate. Nakamura K Ann Plast Surg; 1985 Jan; 14(1):77-80. PubMed ID: 3856414 [TBL] [Abstract][Full Text] [Related]
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100. Agenesis of the corpus callosum and macrocephaly in siblings. Young ID; Trounce JQ; Levene MI; Fitzsimmons JS; Moore JR Clin Genet; 1985 Sep; 28(3):225-30. PubMed ID: 3905089 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]