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Molecular diagnosis of Turner's syndrome.

Turner's syndrome is a common disorder which occurs in around 1/3000 live births in girls. Diagnostic use of polymorphic DNA markers for the X chromosome could help to reduce the number of time consuming karyotype analyses needed. The M27 beta probe maps on the X chromosome to Xcen-Xp11-22 and...

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Bibliografische gegevens
Hoofdauteurs: Gicquel, C, Cabrol, S, Schneid, H, Girard, F, Le Bouc, Y
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: 1992
Onderwerpen:
Online toegang:https://ncbi.nlm.nih.gov/pmc/articles/PMC1016059/
https://ncbi.nlm.nih.gov/pubmed/1355559
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