Editorial
Molecular heterogeneity: a clinical dilemma. Clinical heterogeneity: a molecular dilemma
- PMID: 8317487
- PMCID: PMC1682237
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Editorial
Molecular heterogeneity: a clinical dilemma. Clinical heterogeneity: a molecular dilemma
Am J Hum Genet.
1993 Jul.
No abstract available
Comment on
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Autosomal dominant Marfan-like connective-tissue disorder with aortic dilation and skeletal anomalies not linked to the fibrillin genes.Am J Hum Genet. 1993 Jul;53(1):46-54. Am J Hum Genet. 1993. PMID: 8317497 Free PMC article.
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Mutation in type II procollagen (COL2A1) that substitutes aspartate for glycine alpha 1-67 and that causes cataracts and retinal detachment: evidence for molecular heterogeneity in the Wagner syndrome and the Stickler syndrome (arthro-ophthalmopathy).Am J Hum Genet. 1993 Jul;53(1):55-61. Am J Hum Genet. 1993. PMID: 8317498 Free PMC article.
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