Manuel Mattheisen

Evidence for linkage of the bladder exstrophy-epispadias complex on chromosome 4q31.21-22 and 19q13.31-41 from a consanguineous Iranian family

Research output: Contribution to journal/Conference contribution in journal/Contribution to newspaperJournal articleResearchpeer-review

Standard

Evidence for linkage of the bladder exstrophy-epispadias complex on chromosome 4q31.21-22 and 19q13.31-41 from a consanguineous Iranian family. / Reutter, Heiko; Rüschendorf, Franz; Mattheisen, Manuel; Draaken, Markus; Bartels, Enrika; Hübner, Norbert; Hoffmann, Per; Payabvash, Seyedmedhi; Saar, Kathrin; Nöthen, Markus M; Kajbafzadeh, Abdol-Mohammad; Ludwig, Michael.

In: Birth Defects Research. Part A: Clinical and Molecular Teratology, Vol. 88, No. 9, 09.2010, p. 757-61.

Research output: Contribution to journal/Conference contribution in journal/Contribution to newspaperJournal articleResearchpeer-review

Harvard

Reutter, H, Rüschendorf, F, Mattheisen, M, Draaken, M, Bartels, E, Hübner, N, Hoffmann, P, Payabvash, S, Saar, K, Nöthen, MM, Kajbafzadeh, A-M & Ludwig, M 2010, 'Evidence for linkage of the bladder exstrophy-epispadias complex on chromosome 4q31.21-22 and 19q13.31-41 from a consanguineous Iranian family', Birth Defects Research. Part A: Clinical and Molecular Teratology, vol. 88, no. 9, pp. 757-61. https://doi.org/10.1002/bdra.20701

APA

Reutter, H., Rüschendorf, F., Mattheisen, M., Draaken, M., Bartels, E., Hübner, N., Hoffmann, P., Payabvash, S., Saar, K., Nöthen, M. M., Kajbafzadeh, A-M., & Ludwig, M. (2010). Evidence for linkage of the bladder exstrophy-epispadias complex on chromosome 4q31.21-22 and 19q13.31-41 from a consanguineous Iranian family. Birth Defects Research. Part A: Clinical and Molecular Teratology, 88(9), 757-61. https://doi.org/10.1002/bdra.20701

CBE

Reutter H, Rüschendorf F, Mattheisen M, Draaken M, Bartels E, Hübner N, Hoffmann P, Payabvash S, Saar K, Nöthen MM, Kajbafzadeh A-M, Ludwig M. 2010. Evidence for linkage of the bladder exstrophy-epispadias complex on chromosome 4q31.21-22 and 19q13.31-41 from a consanguineous Iranian family. Birth Defects Research. Part A: Clinical and Molecular Teratology. 88(9):757-61. https://doi.org/10.1002/bdra.20701

MLA

Vancouver

Reutter H, Rüschendorf F, Mattheisen M, Draaken M, Bartels E, Hübner N et al. Evidence for linkage of the bladder exstrophy-epispadias complex on chromosome 4q31.21-22 and 19q13.31-41 from a consanguineous Iranian family. Birth Defects Research. Part A: Clinical and Molecular Teratology. 2010 Sep;88(9):757-61. https://doi.org/10.1002/bdra.20701

Author

Reutter, Heiko ; Rüschendorf, Franz ; Mattheisen, Manuel ; Draaken, Markus ; Bartels, Enrika ; Hübner, Norbert ; Hoffmann, Per ; Payabvash, Seyedmedhi ; Saar, Kathrin ; Nöthen, Markus M ; Kajbafzadeh, Abdol-Mohammad ; Ludwig, Michael. / Evidence for linkage of the bladder exstrophy-epispadias complex on chromosome 4q31.21-22 and 19q13.31-41 from a consanguineous Iranian family. In: Birth Defects Research. Part A: Clinical and Molecular Teratology. 2010 ; Vol. 88, No. 9. pp. 757-61.

Bibtex

@article{ecfbeb5554e941ca838ea09d490fa52a,
title = "Evidence for linkage of the bladder exstrophy-epispadias complex on chromosome 4q31.21-22 and 19q13.31-41 from a consanguineous Iranian family",
abstract = "The bladder exstrophy-epispadias complex (BEEC) is a spectrum of anomalies involving the abdominal wall, pelvis, urinary tract, genitalia, and, occasionally, the spine and anus. Although BEEC typically occurs sporadically, families with two or more affected members have been reported. The present authors previously conducted a genome-wide linkage analysis in two multiply affected (multiplex) families (one of German and one of Spanish origin), which revealed several chromosomal regions compatible with linkage. In the present study, genome-wide linkage analysis was performed in a recently reported consanguineous Iranian multiplex family with an affected sibling pair: a female with epispadias and a male with classic exstrophy of the bladder.",
author = "Heiko Reutter and Franz R{\"u}schendorf and Manuel Mattheisen and Markus Draaken and Enrika Bartels and Norbert H{\"u}bner and Per Hoffmann and Seyedmedhi Payabvash and Kathrin Saar and N{\"o}then, {Markus M} and Abdol-Mohammad Kajbafzadeh and Michael Ludwig",
note = "{\textcopyright} 2010 Wiley-Liss, Inc.",
year = "2010",
month = sep,
doi = "10.1002/bdra.20701",
language = "English",
volume = "88",
pages = "757--61",
journal = "Birth Defects Research",
issn = "1542-9733",
publisher = "John Wiley & Sons, Inc.",
number = "9",

}

RIS

TY - JOUR

T1 - Evidence for linkage of the bladder exstrophy-epispadias complex on chromosome 4q31.21-22 and 19q13.31-41 from a consanguineous Iranian family

AU - Reutter, Heiko

AU - Rüschendorf, Franz

AU - Mattheisen, Manuel

AU - Draaken, Markus

AU - Bartels, Enrika

AU - Hübner, Norbert

AU - Hoffmann, Per

AU - Payabvash, Seyedmedhi

AU - Saar, Kathrin

AU - Nöthen, Markus M

AU - Kajbafzadeh, Abdol-Mohammad

AU - Ludwig, Michael

N1 - © 2010 Wiley-Liss, Inc.

PY - 2010/9

Y1 - 2010/9

N2 - The bladder exstrophy-epispadias complex (BEEC) is a spectrum of anomalies involving the abdominal wall, pelvis, urinary tract, genitalia, and, occasionally, the spine and anus. Although BEEC typically occurs sporadically, families with two or more affected members have been reported. The present authors previously conducted a genome-wide linkage analysis in two multiply affected (multiplex) families (one of German and one of Spanish origin), which revealed several chromosomal regions compatible with linkage. In the present study, genome-wide linkage analysis was performed in a recently reported consanguineous Iranian multiplex family with an affected sibling pair: a female with epispadias and a male with classic exstrophy of the bladder.

AB - The bladder exstrophy-epispadias complex (BEEC) is a spectrum of anomalies involving the abdominal wall, pelvis, urinary tract, genitalia, and, occasionally, the spine and anus. Although BEEC typically occurs sporadically, families with two or more affected members have been reported. The present authors previously conducted a genome-wide linkage analysis in two multiply affected (multiplex) families (one of German and one of Spanish origin), which revealed several chromosomal regions compatible with linkage. In the present study, genome-wide linkage analysis was performed in a recently reported consanguineous Iranian multiplex family with an affected sibling pair: a female with epispadias and a male with classic exstrophy of the bladder.

U2 - 10.1002/bdra.20701

DO - 10.1002/bdra.20701

M3 - Journal article

C2 - 20672349

VL - 88

SP - 757

EP - 761

JO - Birth Defects Research

JF - Birth Defects Research

SN - 1542-9733

IS - 9

ER -