Mapping of Hereditary Trichilemmal Cyst (TRICY1) to Chromosome 3p24-p21.2 and Exclusion of β-CATENIN and MLH1

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Standard

Mapping of Hereditary Trichilemmal Cyst (TRICY1) to Chromosome 3p24-p21.2 and Exclusion of β-CATENIN and MLH1. / Eiberg, Hans; Hansen, Lars; Hansen, Claus; Mohr, Jan; Teglbjærg, Peter Stubbe; Kjaer, Klaus Wilbrandt.

I: American Journal of Medical Genetics, Bind 133 A, Nr. 1, 15.02.2005, s. 44-47.

Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › fagfællebedømt

Harvard

Eiberg, H, Hansen, L, Hansen, C, Mohr, J, Teglbjærg, PS & Kjaer, KW 2005, 'Mapping of Hereditary Trichilemmal Cyst (TRICY1) to Chromosome 3p24-p21.2 and Exclusion of β-CATENIN and MLH1', American Journal of Medical Genetics, bind 133 A, nr. 1, s. 44-47. https://doi.org/10.1002/ajmg.a.30568

APA

Eiberg, H., Hansen, L., Hansen, C., Mohr, J., Teglbjærg, P. S., & Kjaer, K. W. (2005). Mapping of Hereditary Trichilemmal Cyst (TRICY1) to Chromosome 3p24-p21.2 and Exclusion of β-CATENIN and MLH1. American Journal of Medical Genetics, 133 A(1), 44-47. https://doi.org/10.1002/ajmg.a.30568

Vancouver

Eiberg H, Hansen L, Hansen C, Mohr J, Teglbjærg PS, Kjaer KW. Mapping of Hereditary Trichilemmal Cyst (TRICY1) to Chromosome 3p24-p21.2 and Exclusion of β-CATENIN and MLH1. American Journal of Medical Genetics. 2005 feb. 15;133 A(1):44-47. https://doi.org/10.1002/ajmg.a.30568

Author

Eiberg, Hans ; Hansen, Lars ; Hansen, Claus ; Mohr, Jan ; Teglbjærg, Peter Stubbe ; Kjaer, Klaus Wilbrandt. / Mapping of Hereditary Trichilemmal Cyst (TRICY1) to Chromosome 3p24-p21.2 and Exclusion of β-CATENIN and MLH1. I: American Journal of Medical Genetics. 2005 ; Bind 133 A, Nr. 1. s. 44-47.

Bibtex

@article{bdfaa29d4a7044a0ac2ae4224542b191,
title = "Mapping of Hereditary Trichilemmal Cyst (TRICY1) to Chromosome 3p24-p21.2 and Exclusion of β-CATENIN and MLH1",
abstract = "Trichilemmal cysts (also named pilar cyst) derived from the outer root sheath of the deeper parts of the hair follicle can segregate dominantly, and are caused by a yet unknown gene. In order to identify candidate genes for this trait we have ascertained a Danish family with 38 persons (11 affected), and carried out a genome wide scan with 580 DNA micro-satellite markers to identify the locus for a gene, which we termed TRICY1 (for trichilemmal cysts). We found tight linkage to D3S1277 (Z = 4.63; θM = F = 0.00), with flanking markers D3S2432 (Z = 1.59; θM = F = 0.08), and D3S3685 (Z = 2.69; θM = F = 0.08) spanning 10.3 Mb on chromosome 3p24-p21.2. We sequenced two candidate genes previously reported in inherited hair defects, CTNNB1 and MLH1 but failed to detect mutations in exons and intron-exon bounders.",
keywords = "Chromosome 3, Pilar cyst, Trichilemmal cyst",
author = "Hans Eiberg and Lars Hansen and Claus Hansen and Jan Mohr and Teglbj{\ae}rg, {Peter Stubbe} and Kjaer, {Klaus Wilbrandt}",
year = "2005",
month = feb,
day = "15",
doi = "10.1002/ajmg.a.30568",
language = "English",
volume = "133 A",
pages = "44--47",
journal = "American Journal of Medical Genetics, Part A",
issn = "1552-4825",
publisher = "JohnWiley & Sons, Inc.",
number = "1",

}

RIS

TY - JOUR

T1 - Mapping of Hereditary Trichilemmal Cyst (TRICY1) to Chromosome 3p24-p21.2 and Exclusion of β-CATENIN and MLH1

AU - Eiberg, Hans

AU - Hansen, Lars

AU - Hansen, Claus

AU - Mohr, Jan

AU - Teglbjærg, Peter Stubbe

AU - Kjaer, Klaus Wilbrandt

PY - 2005/2/15

Y1 - 2005/2/15

N2 - Trichilemmal cysts (also named pilar cyst) derived from the outer root sheath of the deeper parts of the hair follicle can segregate dominantly, and are caused by a yet unknown gene. In order to identify candidate genes for this trait we have ascertained a Danish family with 38 persons (11 affected), and carried out a genome wide scan with 580 DNA micro-satellite markers to identify the locus for a gene, which we termed TRICY1 (for trichilemmal cysts). We found tight linkage to D3S1277 (Z = 4.63; θM = F = 0.00), with flanking markers D3S2432 (Z = 1.59; θM = F = 0.08), and D3S3685 (Z = 2.69; θM = F = 0.08) spanning 10.3 Mb on chromosome 3p24-p21.2. We sequenced two candidate genes previously reported in inherited hair defects, CTNNB1 and MLH1 but failed to detect mutations in exons and intron-exon bounders.

AB - Trichilemmal cysts (also named pilar cyst) derived from the outer root sheath of the deeper parts of the hair follicle can segregate dominantly, and are caused by a yet unknown gene. In order to identify candidate genes for this trait we have ascertained a Danish family with 38 persons (11 affected), and carried out a genome wide scan with 580 DNA micro-satellite markers to identify the locus for a gene, which we termed TRICY1 (for trichilemmal cysts). We found tight linkage to D3S1277 (Z = 4.63; θM = F = 0.00), with flanking markers D3S2432 (Z = 1.59; θM = F = 0.08), and D3S3685 (Z = 2.69; θM = F = 0.08) spanning 10.3 Mb on chromosome 3p24-p21.2. We sequenced two candidate genes previously reported in inherited hair defects, CTNNB1 and MLH1 but failed to detect mutations in exons and intron-exon bounders.

KW - Chromosome 3

KW - Pilar cyst

KW - Trichilemmal cyst

U2 - 10.1002/ajmg.a.30568

DO - 10.1002/ajmg.a.30568

M3 - Journal article

C2 - 15637721

AN - SCOPUS:12944335173

VL - 133 A

SP - 44

EP - 47

JO - American Journal of Medical Genetics, Part A

JF - American Journal of Medical Genetics, Part A

SN - 1552-4825

IS - 1

ER -

ID: 231917619