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Genetic analysis of the fragile-X mental retardation syndrome with two flanking polymorphic DNA markers.

The fragile-X mental retardation syndrome, one of the most prevalent chromosome X-linked diseases (approximately equal to 1 of 2000 newborn males), is characterized by the presence in affected males and in a portion of carrier females of a fragile site at chromosomes band Xq27. We have performed a l...

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Detalhes bibliográficos
Main Authors: Oberlé, I, Heilig, R, Moisan, J P, Kloepfer, C, Mattéi, G M, Mattéi, J F, Boué, J, Froster-Iskenius, U, Jacobs, P A, Lathrop, G M
Formato: Artigo
Idioma:Inglês
Publicado em: 1986
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Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC323001/
https://ncbi.nlm.nih.gov/pubmed/3006023
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