Zobrazeno 1 - 1
of 1
pro vyhledávání: '"Ronald W Harrison"'
Publikováno v:
Genomics. 34:285-298
Waardenburg syndrome type 1 is caused by mutations in PAX3. Over 50 human PAX3 mutations that lead to hearing, craniofacial, limb, and pigmentation anomalies have been identified. A PAX3 mutant allele, segregating in a family, can show reduced penetr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c6886ae5dae2488a7ec417d35a6cfa54
https://doi.org/10.1006/geno.1996.0289
https://doi.org/10.1006/geno.1996.0289
