1. Two New Loci for Autosomal Recessive Ichthyosis on Chromosomes 3p21 and 19p12- q12 and Evidence for Further Genetic Heterogeneity 
Judith Fischer, Alexandra Faure, Bakar Bouadjar, Claudine Blanchet-Bardon, Aysen Karaduman, Isabelle Thomas, Serap Emre, Susan Cure, Meral Özgüc, Jean Weissenbach, Jean-François Prud'homme 
The American Journal of Human Genetics 
Volume 66, Issue 3, Pages (March 2000)
DOI: /302814
Copyright © 2000 The American Society of Human Genetics Terms and Conditions

2. Figure 1
Pedigrees of six consanguineous nuclear LI families with linkage to chromosome 19. Haplotypes for 29 microsatellite markers from chromosome 19p12-q12 are shown. Affected individuals are indicated by blackened symbols, and the homozygous region that segregates with the disease phenotype is circled.
The American Journal of Human Genetics  , DOI: ( /302814)
Copyright © 2000 The American Society of Human Genetics Terms and Conditions

3. Figure 2
Pedigrees of six consanguineous nuclear NCIE families with linkage to chromosome 3. Haplotypes for 33 microsatellite markers from chromosome 3p21 are shown. Affected individuals are indicated by blackened symbols, and the homozygous region that segregates with the disease phenotype is circled.
The American Journal of Human Genetics  , DOI: ( /302814)
Copyright © 2000 The American Society of Human Genetics Terms and Conditions

4. Figure 3
Limits of the common interval (shaded) in the chromosome 19–linked LI families.
The American Journal of Human Genetics  , DOI: ( /302814)
Copyright © 2000 The American Society of Human Genetics Terms and Conditions

5. Figure 4
Limits of the common interval (shaded) in the chromosome 3–linked NCIE families.
The American Journal of Human Genetics  , DOI: ( /302814)
Copyright © 2000 The American Society of Human Genetics Terms and Conditions