Pages that link to "Q54647114"
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The following pages link to Molecular basis of hypotrichosis with juvenile macular dystrophy in two siblings. (Q54647114):
Displaying 12 items.
- P-cadherin and the journey to cancer metastasis (Q26781906) (← links)
- CDH3-Related Syndromes: Report on a New Mutation and Overview of the Genotype-Phenotype Correlations (Q30410237) (← links)
- Whole Exome Sequencing Reveals Mutations in Known Retinal Disease Genes in 33 out of 68 Israeli Families with Inherited Retinopathies (Q35996537) (← links)
- New CDH3 mutation in the first Spanish case of hypotrichosis with juvenile macular dystrophy, a case report. (Q36243253) (← links)
- Hypotrichosis and juvenile macular dystrophy caused by CDH3 mutation: A candidate disease for retinal gene therapy (Q36881858) (← links)
- Do you know this syndrome? (Q36977784) (← links)
- Genetic diseases of junctions. (Q37002828) (← links)
- The role of P-cadherin in skin biology and skin pathology: lessons from the hair follicle (Q38364407) (← links)
- Phenotypic observations in "hypotrichosis with juvenile macular dystrophy" (recessive CDH3 mutations). (Q38736982) (← links)
- CDH3 gene related hypotrichosis and juvenile macular dystrophy - A case with a novel mutation. (Q47136054) (← links)
- Hypotrichosis with juvenile macular dystrophy: Combination of whole-genome sequencing and genome-wide homozygosity mapping identifies a large deletion in CDH3 initially undetected by whole-exome sequencing-A lesson from next-generation sequencing (Q90330615) (← links)
- Genetic Hair Disorders: A Review (Q92097726) (← links)