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Further evidence localising the gene for Hunter's syndrome to the distal region of the X chromosome long arm.

Cytogenetic re-evaluation of a fibroblast cell line from a female Hunter's syndrome case with a balanced X;autosome translocation, which had previously been reported to have a breakpoint in Xq26 to Xq27, showed the breakpoint to be either between Xq27 and Xq28 or within Xq28. The normal X chrom...

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Detalhes bibliográficos
Publicado no:J Med Genet
Main Authors: Roberts, S H, Upadhyaya, M, Sarfarazi, M, Harper, P S
Formato: Artigo
Idioma:Inglês
Publicado em: BMJ Publishing Group 1989
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC1015597/
https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/2499679/
https://ncbi.nlm.nih.govhttps://doi.org/10.1136/jmg.26.5.309
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