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Gorlin syndrome in a patient with deletion of the distal part of chromosome 9q and fine mapping of the break points with fluorescence in situ hybridization

Publikation: Bidrag til bog/antologi/rapportKonferenceabstrakt i proceedingsForskning

Gorlin syndrome, chromosome 9q, FISH
OriginalsprogEngelsk
TitelIkke angivet
ForlagEuropean Human Genetics Conference 2002, Strasbourg
Publikationsdato2002
Sider201-201
StatusUdgivet - 2002
BegivenhedGorlin syndrome in a patient with deletion of the distal part of chromosome 9q and fine mapping of the break points with fluorescence in situ hybridization -
Varighed: 29 nov. 2010 → …

Konference

KonferenceGorlin syndrome in a patient with deletion of the distal part of chromosome 9q and fine mapping of the break points with fluorescence in situ hybridization
Periode29/11/2010 → …

ID: 34178