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

Odontologisk Institut / Tandlægeskolen

Abstract

Gorlin syndrome, chromosome 9q, FISH

Originalsprog	Engelsk
Titel	Ikke angivet
Forlag	European Human Genetics Conference 2002, Strasbourg
Publikationsdato	2002
Sider	201-201
Status	Udgivet - 2002
Begivenhed	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 - Varighed: 29 nov. 2010 → …

Konference

Konference	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
Periode	29/11/2010 → …

Citationsformater

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. s. 201-201.

Publikation: Bidrag til bog/antologi/rapport › Konferenceabstrakt i proceedings › Forskning

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. i Ikke angivet. European Human Genetics Conference 2002, Strasbourg, s. 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.

@inbook{a7115c7074bf11dbbee902004c4f4f50,

title = "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",

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

author = "S.E. Boonen and Z. T{\"u}mer and Niels Tommerup and D. Stahl and T. Rosenberg and S. Kreiborg and Karen Br{\o}ndum-Nielsen",

year = "2002",

language = "English",

pages = "201--201",

booktitle = "Ikke angivet",

publisher = "European Human Genetics Conference 2002, Strasbourg",

note = "Gorlin syndrome in a patient with deletion of the distal part of chromosome 9q and fine mapping of the break points with fluorescence <i>in situ</i> hybridization ; Conference date: 29-11-2010",

}

TY - ABST

T1 - 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

AU - Boonen, S.E.

AU - Tümer, Z.

AU - Tommerup, Niels

AU - Stahl, D.

AU - Rosenberg, T.

AU - Kreiborg, S.

AU - Brøndum-Nielsen, Karen

PY - 2002

Y1 - 2002

N2 - Gorlin syndrome, chromosome 9q, FISH

AB - Gorlin syndrome, chromosome 9q, FISH

M3 - Conference abstract in proceedings

SP - 201

EP - 201

BT - Ikke angivet

PB - European Human Genetics Conference 2002, Strasbourg

T2 - Gorlin syndrome in a patient with deletion of the distal part of chromosome 9q and fine mapping of the break points with fluorescence <i>in situ</i> hybridization

Y2 - 29 November 2010

ER -