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Association between c135G/A genotype and RET proto-oncogene germline mutations and phenotype of Hirschsprung's disease.

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Association between c135G/A genotype and RET proto-oncogene germline mutations and phenotype of Hirschsprung's disease. / Fitze, Guido; Cramer, Jakob; Ziegler, Andreas; Schierz, Mandy; Schreiber, Matthias; Kuhlisch, Eberhard; Roesner, Dietmar; Schackert, Hans K.

In: LANCET, Vol. 359, No. 9313, 9313, 2002, p. 1200-1205.

Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review

Harvard

Fitze, G, Cramer, J, Ziegler, A, Schierz, M, Schreiber, M, Kuhlisch, E, Roesner, D & Schackert, HK 2002, 'Association between c135G/A genotype and RET proto-oncogene germline mutations and phenotype of Hirschsprung's disease.', LANCET, vol. 359, no. 9313, 9313, pp. 1200-1205. <http://www.ncbi.nlm.nih.gov/pubmed/11955539?dopt=Citation>

APA

Fitze, G., Cramer, J., Ziegler, A., Schierz, M., Schreiber, M., Kuhlisch, E., Roesner, D., & Schackert, H. K. (2002). Association between c135G/A genotype and RET proto-oncogene germline mutations and phenotype of Hirschsprung's disease. LANCET, 359(9313), 1200-1205. [9313]. http://www.ncbi.nlm.nih.gov/pubmed/11955539?dopt=Citation

Vancouver

Fitze G, Cramer J, Ziegler A, Schierz M, Schreiber M, Kuhlisch E et al. Association between c135G/A genotype and RET proto-oncogene germline mutations and phenotype of Hirschsprung's disease. LANCET. 2002;359(9313):1200-1205. 9313.

Bibtex

@article{72dcae1d6421404f85a0430f9abf91fc,
title = "Association between c135G/A genotype and RET proto-oncogene germline mutations and phenotype of Hirschsprung's disease.",
abstract = "Several genes, including the major susceptibility gene RET, have roles in development of Hirschsprung's disease. Results of genetic-linkage analysis of patients with familial disease with both long-segment and short-segment phenotypes have shown close linkage with the RET locus. We aimed to investigate whether both RET mutations and polymorphisms contribute to phenotype of Hirschsprung's disease.",
author = "Guido Fitze and Jakob Cramer and Andreas Ziegler and Mandy Schierz and Matthias Schreiber and Eberhard Kuhlisch and Dietmar Roesner and Schackert, {Hans K}",
year = "2002",
language = "Deutsch",
volume = "359",
pages = "1200--1205",
journal = "LANCET",
issn = "0140-6736",
publisher = "Elsevier Limited",
number = "9313",

}

RIS

TY - JOUR

T1 - Association between c135G/A genotype and RET proto-oncogene germline mutations and phenotype of Hirschsprung's disease.

AU - Fitze, Guido

AU - Cramer, Jakob

AU - Ziegler, Andreas

AU - Schierz, Mandy

AU - Schreiber, Matthias

AU - Kuhlisch, Eberhard

AU - Roesner, Dietmar

AU - Schackert, Hans K

PY - 2002

Y1 - 2002

N2 - Several genes, including the major susceptibility gene RET, have roles in development of Hirschsprung's disease. Results of genetic-linkage analysis of patients with familial disease with both long-segment and short-segment phenotypes have shown close linkage with the RET locus. We aimed to investigate whether both RET mutations and polymorphisms contribute to phenotype of Hirschsprung's disease.

AB - Several genes, including the major susceptibility gene RET, have roles in development of Hirschsprung's disease. Results of genetic-linkage analysis of patients with familial disease with both long-segment and short-segment phenotypes have shown close linkage with the RET locus. We aimed to investigate whether both RET mutations and polymorphisms contribute to phenotype of Hirschsprung's disease.

M3 - SCORING: Zeitschriftenaufsatz

VL - 359

SP - 1200

EP - 1205

JO - LANCET

JF - LANCET

SN - 0140-6736

IS - 9313

M1 - 9313

ER -