');document.write('Genetics Home Reference
');document.write('Leber congenital amaurosis
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Leber congenital amaurosis and its relationship with genes CEP290, CRB1, GUCY2D, and RPE65 have been added to Genetics Home Reference. Web links to MedlinePlus, NIH publications, patient support web sites, Gene Reviews, Gene Tests, ClinicalTrials.gov, PubMed, and OMIM are included.

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');document.write('CHMP2B-related frontotemporal dementia
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CHMP2B-related frontotemporal dementia and its relationship with gene CHMP2B have been added to Genetics Home Reference. Web links to MedlinePlus, NIH publications, patient support web sites, Gene Reviews, ClinicalTrials.gov, PubMed, and OMIM are included.

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');document.write('X-linked lymphoproliferative disease
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X-linked lymphoproliferative disease and its relationship with genes SH2D1A and XIAP have been added to Genetics Home Reference. Web links to MedlinePlus, NIH publications, patient support web sites, Gene Reviews, Gene Tests, ClinicalTrials.gov, PubMed, and OMIM are included.

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');document.write('Miller syndrome
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Miller syndrome and its relationship with gene DHODH have been added to Genetics Home Reference. Web links to MedlinePlus, patient support web sites, ClinicalTrials.gov, PubMed, and OMIM are included.

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');document.write('familial paroxysmal kinesigenic dyskinesia
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Familial paroxysmal kinesigenic dyskinesia has been added to Genetics Home Reference. Web links to MedlinePlus, patient support web sites, Gene Reviews, ClinicalTrials.gov, PubMed, and OMIM are included.

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');document.write('primary ciliary dyskinesia
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Primary ciliary dyskinesia and its relationship with genes DNAH5 and DNAI1 have been added to Genetics Home Reference. Web links to MedlinePlus, Genetic and Rare Diseases Information Center, NIH publications, patient support web sites, Gene Reviews, Gene Tests, ClinicalTrials.gov, PubMed, and OMIM are included.

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');document.write('lamellar ichthyosis
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Lamellar ichthyosis and its relationship with genes ABCA12 and TGM1 have been added to Genetics Home Reference. Web links to MedlinePlus, patient support web sites, Gene Reviews, Gene Tests, ClinicalTrials.gov, PubMed, and OMIM are included.

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');document.write('nonbullous congenital ichthyosiform erythroderma
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Nonbullous congenital ichthyosiform erythroderma and its relationship with genes ALOX12B and ALOXE3 have been added to Genetics Home Reference. Web links to MedlinePlus, patient support web sites, Gene Reviews, Gene Tests, ClinicalTrials.gov, PubMed, and OMIM are included.

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');document.write('mucopolysaccharidosis type III
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Mucopolysaccharidosis type III and its relationship with genes GNS, HGSNAT, NAGLU, and SGSH have been added to Genetics Home Reference. Web links to MedlinePlus, Genetic and Rare Diseases Information Center, NIH publications, patient support web sites, Gene Tests, ClinicalTrials.gov, PubMed, and OMIM are included.

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');document.write('mucopolysaccharidosis type VII
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Mucopolysaccharidosis type VII and its relationship with gene GUSB have been added to Genetics Home Reference. Web links to MedlinePlus, NIH publications, patient support web sites, Gene Tests, ClinicalTrials.gov, PubMed, and OMIM are included.

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');document.write('Lennox-Gastaut syndrome
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Lennox-Gastaut syndrome has been added to Genetics Home Reference. Web links to MedlinePlus, NIH publications, patient support web sites, ClinicalTrials.gov, PubMed, and OMIM are included.

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');document.write('Moebius syndrome
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Moebius syndrome has been added to Genetics Home Reference. Web links to MedlinePlus, NIH publications, patient support web sites, ClinicalTrials.gov, PubMed, and OMIM are included.

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