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Results: 3

1.
Figure  2

Figure 2. From: The Gene for Juvenile Hyaline Fibromatosis Maps to Chromosome 4q21.

Hands of ID 7, showing nodular lesions and subcutaneous swellings that are typical of JHF

Nazneen Rahman, et al. Am J Hum Genet. 2002 October;71(4):975-980.
2.
Figure  3

Figure 3. From: The Gene for Juvenile Hyaline Fibromatosis Maps to Chromosome 4q21.

Combined multipoint LOD score at chromosome 4q21 in five families with JHF

Nazneen Rahman, et al. Am J Hum Genet. 2002 October;71(4):975-980.
3.
Figure  1

Figure 1. From: The Gene for Juvenile Hyaline Fibromatosis Maps to Chromosome 4q21.

Haplotypes for 13 markers from chromosome 4q21 in five families with JHF. Blackened symbols indicate individuals affected with JHF. In families A–D, boxes around marker alleles indicate the region of homozygosity. In family E, all vertical bars next to the alleles indicate the segregating haplotypes and show that the parental chromosome 4q21 haplotypes inherited by the affected individual (ID 26) are different from those of his unaffected siblings. Critical meiotic recombinants in ID 11, ID 22, and ID 23 refine the minimal interval encompassing the JHF-predisposition gene to the region between D4S2393 and D4S395.

Nazneen Rahman, et al. Am J Hum Genet. 2002 October;71(4):975-980.

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