The Novel Genetic Disorder Microhydranencephaly Maps to Chromosome 16p

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The Novel Genetic Disorder Microhydranencephaly Maps to Chromosome 16p13.3- 12.1 Gül Nihan Kavaslar, Suna Önengüt, Orhan Derman, Ahmet Kaya, Aslıhan Tolun The American Journal of Human Genetics Volume 66, Issue 5, Pages 1705-1709 (May 2000) DOI: 10.1086/302898 Copyright © 2000 The American Society of Human Genetics Terms and Conditions

Figure 1 Haplotypes for 11 markers at 16p, for affected branches of the family. Marker order and relative distances (minimal to maximal [in cM]) are D16S2616-(1–1.5)-D16S418-(1.5–7)-16S497-(0–1)-D16S748-(2–3)-D16S764-(5–6)-D16S535-(0)-D16S490-(2)-D16S672-(8)-D16S769-(13)-D16S690-(11)-D16S3396, as deduced from Genome Database. The marker D16S403 maps somewhere in the region of markers D16S535, D16S490, and D16S672. The American Journal of Human Genetics 2000 66, 1705-1709DOI: (10.1086/302898) Copyright © 2000 The American Society of Human Genetics Terms and Conditions

Figure 2 Photographs of patient 1 (A and B), patient 2 (C), and patient 3 (D) The American Journal of Human Genetics 2000 66, 1705-1709DOI: (10.1086/302898) Copyright © 2000 The American Society of Human Genetics Terms and Conditions