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

S.E. Boonen; Z. Tümer; Niels Tommerup; D. Stahl; T. Rosenberg; S. Kreiborg; Karen Brøndum-Nielsen

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

S.E. Boonen, Z. Tümer, Niels Tommerup, D. Stahl, T. Rosenberg, S. Kreiborg, Karen Brøndum-Nielsen

Department of Odontology

Abstract

Gorlin syndrome, chromosome 9q, FISH

Original language	English
Title of host publication	Ikke angivet
Publisher	European Human Genetics Conference 2002, Strasbourg
Publication date	2002
Pages	201-201
Publication status	Published - 2002
Event	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 - Duration: 29 Nov 2010 → …

Conference

Conference	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
Period	29/11/2010 → …

Cite this

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. / Boonen, S.E.; Tümer, Z.; Tommerup, Niels et al.

Ikke angivet. European Human Genetics Conference 2002, Strasbourg, 2002. p. 201-201.

Research output: Chapter in Book/Report/Conference proceeding › Conference abstract in proceedings › Research

Boonen, SE, Tümer, Z, Tommerup, N, Stahl, D, Rosenberg, T, Kreiborg, S & Brøndum-Nielsen, K 2002, 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. in Ikke angivet. European Human Genetics Conference 2002, Strasbourg, pp. 201-201, 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, 29/11/2010.

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abstract = "Gorlin syndrome, chromosome 9q, FISH",

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AU - Brøndum-Nielsen, Karen

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